Buenos Aires, Argentina
Cincinnati, USA
Leipzig, Germany
Thu 27 08:00
WG2.1
Stockholm, Sweden
Thu 27 08:30
WG2.2
Impaired fasting glycaemia in pediatric obesity and type 2 diabetes in young adulthood
Stockholm, Sweden
Heidelberg, Germany
Bern, Switzerland
Petah Tikva, Israel
Thu 27 09:25
WG4.6
Updates on the developments of Decision Support Systems for the treatment of diabetes
Petah Tikva, Israel
Thu 27 13:00
SS1.3
Interaction between nutrition, the endocrine system and the growth plate
Petah Tikva, Israel
Skopje, Macedonia
Thu 27 09:45
WG4.7
Use of social media for improving glucose control in patients with type 1 diabetes
Skopje, Macedonia
Cambridge, UK
Cincinnati, USA
Stockholm, Sweden
Thu 27 12:00
SS1.1
Petah Tikva, Israel
Thu 27 09:25
WG4.6
Updates on the developments of Decision Support Systems for the treatment of diabetes
Petah Tikva, Israel
Thu 27 13:00
SS1.3
Interaction between nutrition, the endocrine system and the growth plate
Petah Tikva, Israel
Tubingen, Germany
Thu 27 15:20
HDI1.2
…Differentiate between constitutional delay in growth and puberty and hypog hypog?
Tubingen, Germany
Cambridge, UK
Thu 27 15:40
HDI1.3
Munich, Germany
Fri 28 12:00
PL4
Genoa, Italy
Melbourne, Australia
Sat 29 09:20
HDI2.2
...Manage a child with physical disabilities who has a low bone mineral density
Melbourne, Australia
Poznań, Poland
Sat 29 09:40
HDI2.3
Dresden, Germany
London, UK
Bethesda, USA
Sat 29 17:30
PL8
Hebron, Palestine
Thu 27 16:25
RFC2.6
The novel R211Q POP1 homozygous mutation causes severe short stature but uniquely only subtle skeletal dysplasia.
Hebron, Palestine
Glasgow, United Kingdom
Fri 28 10:45
ERN1.5
EuRRECa - European Registries For Rare Endocrine Conditions
Glasgow, United Kingdom
Sat 29
AC1.1
The ESPE roadmap to a career in academic paediatric endocrinology
Glasgow, United Kingdom
Sat 29
AC1.2
Glasgow, UK
Odense, Denmark
Thu 27 16:05
RFC2.2
S-25OHD is Associated with Hand Grip Strength and Myopathy at Five Years in Girls: An Odense Child Cohort Study.
Odense, Denmark
Athens, Greece
Sat 29 15:30
S10.1
Moscow, Russian Federation
Thu 27 16:15
RFC5.4
The value of cytological, histological and US examination to determine of management children with nodular goiter.
Moscow, Russian Federation
Barcelona, Spain
Madrid, Spain
Thu 27 16:00
RFC4.1
Metabolomic changes in patients with PAPP-A2 deficiency in response to rhIGF1 treatment.
Madrid, Spain
Ioannina, Greece
Bern, Switzerland
Messina, Italy
Athens, Greece
Sat 29 10:00
RFC14.1
Psychometric and Psycho-social Profile of Children and Adolescent Survivors of Pediatric Cancer.
Athens, Greece
Paris, France
Sat 29
YI1.1
Ljubljana, Slovenia
Kolding, Denmark
Sat 29 10:10
RFC11.3
Increased levels of bone formation and resorption markers in patients with hypophosphatemic rickets.
Kolding, Denmark
Paris, France)
Thu 27 15:00
FC3.1
Neonatal diabetes owned to potassium channel mutation: response to sulfonylureas according to the genotype.
Paris, France)
Sat 29 10:25
RFC12.6
AMGLIDIA, a suspension of glibenclamide for patients with neonatal diabetes, long term data on efficiency and tolerance.
Paris, France)
New York, USA
't Harde, The Netherlands
't Harde, The Netherlands
Sheffield, UK
Sheffield, UK
Rome, Italy
Katowice, Poland
Sat 29 09:40
FC15.5
Utility of BDNF and MMP-1 as markers of cardiometabolic risk in Turner syndrome girls.
Katowice, Poland
Newcastle, UK
Thu 27 15:50
FC2.6
Białystok, Poland
Bristol, UK
Ulm, Germany
Fri 28 10:10
FC6.5
Copenhagen, Denmark
Sat 29 10:20
RFC13.5
Pubertal voice break: Temporal relation of secondary sexual characteristics in healthy boys.
Copenhagen, Denmark
Michigan, USA
Thu 27 12:00
S1.1
The molecular basis of Combined Pituitary Hormone Deficiency: lessons from animal models
Michigan, USA
Fri 28
NA1.2
Cardiff, UK
São Paulo, Brazil
Fri 28 10:30
RFC9.1
Clinical and genetic features of central precocious puberty associated with complex phenotypes.
São Paulo, Brazil
Paris, France
Paris, France
Indiana, USA
Paris, France
London, UK
Fri 28 10:55
RFC9.6
Can neuroimagine predict endocrine morbidity in congenital hypothalamo-pituitary (H-P) disorders?
London, UK
Vancouver, Canada
Vancouver, Canada
Athens, Greece
Pittsburgh, USA
Fri 28
S4.3
Glasgow, UK
Sat 29 10:20
RFC11.5
Seoul, Republic of Korea
Thu 27 16:20
RFC4.5
12-Month effects of once-weekly and twice-monthly administration of hybrid Fc-fused human growth hormone, GX-H9, treatment in pediatric with GHD deficiency.
Seoul, Republic of Korea
Madrid, Spain
Rome, Italy
North Carolina, USA
Fri 28
S6.1
The biology of the glucocorticoid receptor: new signaling mechanisms in health and disease
North Carolina, USA
Reggio Emilia, Italy
Paris, France
Haifa, Israel
Sat 29 10:10
RFC12.3
Barriers and sources of support for the performance of physical activity inpediatric type 1 diabetes.
Haifa, Israel
Nice, France
New Haven, USA
Sat 29 09:10
FC13.2
London, UK
Thu 27 15:50
FC1.6
London, UK
Birmingham, UK
Bristol, UK
Zagreb, Croatia
Sat 29 10:15
RFC11.4
A new form of Anhidrotic Ectodermal Dysplasia with Immunodeficiency caused by abolished Store-Operated Ca2+ Entry.
Zagreb, Croatia
Rotterdam, The Netherlands
Thu 27 16:25
RFC4.6
Effect of 2 years of Growth Hormone Treatment on Glucose Tolerance in Adults with Prader-Willi Syndrome.
Rotterdam, The Netherlands
London, UK
Rotterdam, The Netherlands
Sat 29 09:50
FC13.6
Teamwork saves lives: how pediatric multidisciplinary care can prevent ‘unexplained deaths’ in adults with Prader-Willi syndrome.
Rotterdam, The Netherlands
London, UK
Ulm, Germany
Glasgow, UK
Thu 27 09:52
WG1.6
London, UK
Tampa, USA
Montréal, Canada
Thu 27 16:25
RFC5.6
DUOX2 Deficiency in Quebec: From Life-threatening Compressive Goiter in Infancy to Lifelong Euthyroidism.
Montréal, Canada
Cairo, Egypt
Sat 29 09:40
FC12.5
Effect of Homocysteine-Lowering Therapy on Diabetic Nephropathy in Children and Adolescents with Type 1 Diabetes.
Cairo, Egypt
Bari, Italy
Fri 28 10:55
RFC6.6
Nicosia, Cyprus
Sat 29 09:00
FC13.1
Nancy, France
Fri 28 09:40
FC8.2
Partial restoration of biological effects of estrogen in a female with estrogen receptor α variant.
Nancy, France
Boston, USA
Cincinnati, USA
Haifa, Israel
Thu 27 15:40
FC4.5
Prediction of adult height by artificial intelligence (AI) through machine learning (ML) from early height data.
Haifa, Israel
Paris, France
Lille, France
Athens, Greece
London, UK
Thu 27 09:30
WG5.5
London, UK
Sao Paulo, Brazil
Fri 28 10:10
FC8.5
DEAH-box helicase 37defects (DXH37) deffects are a Novel Cause of 46,XY Gonadal Dysgenesis.
Sao Paulo, Brazil
Nijmegen, The Netherlands
London, UK
Fri 28 09:50
FC9.3
Mutations in MAGEL2 and L1CAM are associated with congenital hypopituitarism and arthrogryposis.
London, UK
Southborough, UK
Fri 28 10:05
ERN1.3
Ghent, Belgium
Ramat Gan, Israel
Fri 28 10:20
FC10.6
Primary ovarian insufficiency incidence rate and etiology among Israeli adolescents between the years 2000-2016 – A multi-center study
Ramat Gan, Israel
Moscow, Russian Federation
Fri 28 10:30
RFC7.1
Next generation sequencing results in 142 patients with congenital hyperinsulinism.
Moscow, Russian Federation
Madrid, Spain
London, UK
Fri 28 09:50
FC10.3
Istanbul, Turkey
Liestal, Switzerland
Udevalla, Sweden
Copenhagen, Denmark
Fri 28 10:10
FC7.5
Thyroid hormone levels in cord blood are associated with fetal and neonatal growth.
Copenhagen, Denmark
Holon, Israel
Sat 29 10:25
RFC14.6
Identification of epithelial sodium channel (ENaC) in endometrial pipelle biopsy samples.
Holon, Israel
Edmonton, Canada
Haifa, Isreal)
Birmingham, UK
Leipzig, Germany
London, UK
Thu 27 15:40
FC5.5
Guidelines for the Management of Paediatric Differentiated Thyroid Carcinoma; a UK endeavour.
London, UK
Sat 29 09:20
FC13.3
Cambridge, UK
Doha, Qatar
Fri 28
YB2.5
Birmingham, UK
Thu 27 16:15
RFC1.4
Mass spectrometry-based assessment of childhood androgen excess in 487 consecutive patients over 5 years.
Birmingham, UK
Tokyo, Japan
Rome, Italy
Varna, Bulgaria
Sat 29
AC1.4
London, UK
Sat 29 09:50
FC15.6
Oxford, UK
Glasgow, UK
Copenhagen, Denmark
Giessen, Germany
Sparta, Greece
Sat 29 09:10
FC12.2
Apoptosis and oxidative stress markers during the Oral Glucose Tolerance Test (OGTT).
Sparta, Greece
London, UK
Buenos Aires, Argentina
Thu 27 15:00
FC4.1
Monogenic and digenic gene mutations are present in children with idiopathic short stature (ISS).
Buenos Aires, Argentina
Amsterdam, The Netherlands
Thu 27 16:00
RFC1.1
The relative contributions of genetic and environmental factors on cortisol metabolism at pre-, mid- and post-pubertal ages.
Amsterdam, The Netherlands
Leipzig, Germany
Doha, Qatar
Leipzig, Germany
Fri 28 09:50
FC6.3
Gothenburg, Sweden
Fri 28 10:35
RFC6.2
IGF-I at four months associates to visceral and subcutaneous adipose tissue at 7 years of age.
Gothenburg, Sweden
Patras, Greece
Geneva, Switzerland
Sat 29 10:15
RFC12.4
Use of telemonitoring via a mobile device app reduces HbA1c in type 1 diabetic children and adolescents.
Geneva, Switzerland
Amsterdam, The Netherlands
Fri 28 10:55
RFC8.6
Metabolic profile of young adult transgender persons who started gender affirming treatment in their adolescence.
Amsterdam, The Netherlands
Hannover, Germany
Thu 27 17:15
MTE4.1
Sat 29
MTE4.2
Berlin, Germany
Sat 29 16:30
S10.3
Munich, Germany
Kiel, Germany
Thessaloniki, Greece
Thu 27 15:50
FC5.6
Alterations in DNA methylation status of gene promoters in children and adolescents with autoimmune thyroid disease.
Thessaloniki, Greece
Helsinki, Finland
Thu 27 15:20
FC2.3
Clinical course of hypoparathyroidism in patients with APECED (APS1)
Helsinki, Finland
Hannover, Germany
Fri 28 08:30
MTE8.1
Sat 29 14:00
MTE8.2
Philadelphia, USA
Thu 27 15:10
FC2.2
Whole genome sequencing reveals novel intragenic deletions of GNAS as causes of pseudohypoparathyroidism type 1a.
Philadelphia, USA
Sat 29 09:40
FC11.5
A recurrent 6-bp intronic deletion in NESP55 with reduced penetrance in pseudohypoparathyroidism type 1b.
Philadelphia, USA
Sheffield, UK
Sat 29 09:30
FC14.4
Glucocorticoid deficiency causes differentially dysregulated oxidative stress depending on the steroidogenic defects.
Sheffield, UK
Paris, France
Sat 29 15:30
S7.1
Paris, France
Thu 27 09:40
WG3.5
Groningen, The Netherlands
Sat 29 16:30
S8.3
Paediatric differentiated thyroid cancer: outcome and long term effects
Groningen, The Netherlands
Beijing, China
Örebro, Sweden
Rotterdam, The Netherlands
Thu 27 12:00
S2.1
The biology of germ cell tumors in Disorders of Sex Development
Rotterdam, The Netherlands
Girona, Spain
Mexico City, Mexico
Sat 29 10:25
RFC11.6
Reference Values of Automated Bone Age and Bone Health Index for Mexican children and adolescents.
Mexico City, Mexico
Herlev, Denmark
Sat 29 10:05
RFC12.2
Bone mineral density is increased in 276 Danish children and adolescents with Type-1-Diabetes.
Herlev, Denmark
Helsinki, Finland
Fri 28
YB2.1
Montreal, Canada
Thu 27 15:10
FC3.2
Genome-Wide Meta-Analysis identifies a novel low frequency STK39 variant of large effect on risk of Type 1 Diabetes.
Montreal, Canada
Madrid, Spain
London, United Kingdom
Fri 28 10:35
RFC7.2
Outcomes of a quality improvement project integrating Continuous Glucose Monitoring Systems into the routine management of neonatal hypoglycaemia.
London, United Kingdom
Cleveland, USA
Sat 29 10:00
RFC12.1
Use of acid-suppressive medications during infancy and early childhood and its association with type 1 diabetes.
Cleveland, USA
Fribourg, Switzerland
Fri 28 10:00
FC8.4
STARD8, a novel candidate gene for 46,XY disorders of sex development.
Fribourg, Switzerland
Copenhagen, Denmark
Minneapolis, USA
Sat 29 10:20
RFC15.5
Effect of Adjusting for Tanner Stage Age on Short and Tall Stature Prevalence in US Youths.
Minneapolis, USA
Edinburgh, UK
Thessaloniki, Greece
Sat 29 10:20
RFC12.5
Insulin gene promoter methylation status in Greek children and adolescents with Type 1 Diabetes.
Thessaloniki, Greece
South Brisbane, Australia
Sat 29 10:10
RFC14.3
Dysregulated glucose homeostasis in Congenital Central Hypoventilation Syndrome.
South Brisbane, Australia
Genoa, Italy
Fri 28 10:55
RFC7.6
Assessment of Pituitary Stalk Anatomy by T2 DRIVE without Gadolinium in Pituitary Diseases.
Genoa, Italy
Nicosia, Cyprus
Thu 27 16:20
RFC5.5
Evidence for a founder effect in Multiple Endocrine Neoplasia 2.
Nicosia, Cyprus
Paris, France
Athens, Greece
Saint-Petersburg, Russian Federation
Sat 29 09:40
FC13.5
Study of the serum kisspeptin level in healthy and hypogonadotropic boys.
Saint-Petersburg, Russian Federation
Stockholm, Sweden
Petah Tikva, Israel
São Paulo, Brazil
Sat 29 09:30
FC15.4
Ulm, Germany
Fri 28 10:45
RFC6.4
Functionality and phenotypic characteristics of mutations in the human leptin receptor.
Ulm, Germany
Sheffield, United Kingdom
Fri 28 10:20
FC8.6
The roles of steroids in gonadal development and maintenance – insights from a zebrafish model of androgen and cortisol deficiency.
Sheffield, United Kingdom
Cork, Ireland
Montreal, Canada
Sheffield, UK
Cambridge, UK
Thu 27 16:20
RFC3.5
Recent secular change in pre- and postnatal growth and adiposity in Infants of Mothers with Gestational Diabetes.
Cambridge, UK
Campinas, Brazil
Cambridge, United Kingdom
Chengdu, China
Sat 29 10:10
RFC13.3
Circulating MKRN3, Kisspeptin and IGF-1 levels in girls during the clinical onset of puberty.
Chengdu, China
Suita, Japan
Manchester, UK
Athens, Greece
Athens, Greece
Sat 29 10:15
RFC13.4
Liège, Belgium
Bern, Switzerland
Thu 27 16:05
RFC1.2
Changes in CYP19A1 and CYP3A4 activities due to population genetic variations in human P450 Oxidoreductase.
Bern, Switzerland
Adelaide, Australia
North Adelaide, Australia
Sat 29 09:50
FC12.6
Persistent beneficial effects of metformin in children and adolescents with type 1 diabetes: Adelaide metformin randomized controlled trial follow up.
North Adelaide, Australia
Buenos Aires, Argentina
Thu 27 15:10
FC4.2
Effects of IGF-1R nuclear localization in glioblastoma cells.
Buenos Aires, Argentina
Manchester, UK
Sat 29 09:00
FC15.1
The diagnostic yield of a targeted next generation sequencing panel in children with short stature of undefined aetiology.
Manchester, UK
Israel
Tel Aviv, Israel
Lausanne, Switzerland
Santiago, Chile
Thu 27 16:10
RFC4.3
A deletion encompassing exon 2 of the alsgene: Analysis of a patient with ALS deficiency and his family.
Santiago, Chile
Prague, Czech Republic
Thu 27 16:10
RFC3.3
Significant prevalence of severe monogenic immune defects among children with Type 1 diabetes and low T1D-genetic risk score.
Prague, Czech Republic
London, UK
Thu 27 15:50
FC3.6
Using CRISPR/Cas9gene editing to study the molecular genetics of Congenital Hyperinsulinism.
London, UK
Vienna, Austria
Sat 29 09:10
FC11.2
Helsinki, Finland
Vellore, India
Thu 27 15:40
FC2.5
Radial ESWT stimulates longitudinal bone growth in cultured rat fetal metatarsal bones.
Vellore, India
Søborg, Denmark
Thu 27 15:50
FC4.6
Absorption and Excretion of Somapacitan, a Long-Acting Growth Hormone (GH) Derivative.
Søborg, Denmark
Manchester, UK
Munich, Germany
Fri 28 10:25
ERN1.4
London, UK
Virginia, USA
Oregon, USA
Seattle, USA
Fri 28 09:40
FC6.2
Paris, France
Ankara, Turkey
Sat 29 09:30
FC12.4
How does thiol/disulphide homeostasis change in children with type 1 diabetesmellitus?
Ankara, Turkey
Parkville, Australia
Fri 28 10:30
RFC6.1
Allelic variation in key fitness genes is linked with increased severity of obesity in overweight/obese youth.
Parkville, Australia
Stockholm, Sweden
Ghent, Belgium
Bonn, Germany
Freiburg, Germany
Sat 29 10:25
RFC13.6
Close correlation between salivary and blood steroids in normal boys: Salivary testosterone best characterizes male puberty.
Freiburg, Germany
Geneva, Switzerland
Thu 27 16:05
RFC3.2
Personalized and predictive medicine for pediatric diabetes through a genetic test using next generation sequencing.
Geneva, Switzerland
Rehovot, Israel
Athens, Greece
Bethesda, USA
Sat 29 10:15
RFC14.4
A novel germline DICER1 mutation in a girl with multinodular goiter and ovarian Sertoli-Leydig cell tumor.
Bethesda, USA
Ankara, Turkey
Sat 29 10:05
RFC11.2
New York, USA
Fri 28
S4.2
Stockholm, Sweden
Fribourg, Switzerland
Fri 28 09:30
FC8.1
Estrogen Receptor 2 Variant as a Novel Cause for Dysgenetic Ovaries.
Fribourg, Switzerland
Bratislava, Slovakia
Sat 29
YI1.2
Adipokines and genetic markers of childhood obesity and insulin resistance
Bratislava, Slovakia
Amsterdam, The Netherlands
Thu 27 08:05
WG6.1
Gender identity development: Neither male nor female or being both, growing up as gender queer
Amsterdam, The Netherlands
Ljubljana, Slovenia
Fri 28 10:35
RFC9.2
Novel variant in GNRHR gene regulatory region in a pedigree with maternally inherited precocious puberty.
Ljubljana, Slovenia
Greece
Fri 28 08:00
PL3
Sacramento, USA
Basel, Switzerland
Lübeck, Germany
Sat 29 10:00
RFC11.1
Diagnosis and management of pseudohypoparathyroidism and related disorders: First international consensus statement.
Lübeck, Germany
Amsterdam, The Netherlands
Istanbul, Turkey
Bern, Switzerland
Fri 28 10:00
FC7.4
Altered substrate specificities and metabolite production by aromatase (CYP19A1) due to the R192H mutation.
Bern, Switzerland
Tokyo, Japan
Rotterdam, The Netherlands
Fri 28
S5.1
Kaunas, Lithuania
Bern, Switzerland
Utrecht, The Netherlands
Sat 29 10:20
RFC14.5
Natural course of MEN type 2B syndrome; a Dutch single-center cohort.
Utrecht, The Netherlands
Rotterdam, The Netherlands
Petah Tikva, Israel
Thu 27 09:10
WG5.4
Endocrine-metabolic outcome of women with a history of sexual precocity
Petah Tikva, Israel
Leiden, The Netherlands
Thu 27 09:30
WG6.3
Fertility preservation in transgender adolescents: an ethical perspective. Is the sky the limit?
Leiden, The Netherlands
Ankara, Turkey
Germany
Edinburgh, UK
Fri 28
PL5
Dynamic control of tissue glucocorticoids – lessons for optimising replacement therapy
Edinburgh, UK
Edinburgh, UK
Paris, France
Fri 28 10:50
RFC9.5
Non-isolated central precocious puberty: prevalence of brain lesions and other associated disorders.
Paris, France
London, UK
Stockholm, Sweden
Leiden, The Netherlands
Thu 27 12:30
SS1.2
Fascinating growth phenomena: what causes individual catch-up growth and population secular change
Leiden, The Netherlands
Erlangen, Germany
Chicago, USA
Manchester, UK
Sat 29 09:30
FC11.4
Using patient derived induced pluripotent stem cells to model multiple epiphyseal dysplasia.
Manchester, UK
Freiburg, Germany
London, UK
Manchester, UK
Fri 28 10:40
RFC7.3
Central venous cathether-associated thrombosis in children with congenital hyperinsulinism.
Manchester, UK
Leuven, Belgium
Thu 27 09:00
WG2.3
Hangzhou, China
Thu 27 15:30
FC2.4
Diagnostic Performance of Artificial Neural Network-Based TW3 Skeletal Maturity Assessment.
Hangzhou, China
Basel, Switzerland
Adrenal cortex (to include Cushing’s)
Adrenals and HPA Axis
Bone, growth plate and mineral metabolism
GH and IGFs
Pituitary, neuroendocrinology and puberty
Fetal, neonatal endocrinology and metabolism (to include hypoglycaemia)
Sex differentiation, gonads and gynaecology or sex endocrinology
Diabetes and insulin
Growth and syndromes (to include Turner syndrome)
Multisystem endocrine disorders
Thyroid
Fat, metabolism and obesity
FC1.1
A novel non-invasive Short Synacthen Test validated in a healthy paediatric population
Charlotte Elder, Ruben Vilela, Trevor Johnson, E Helen Kemp, Brian Keevil, John Newell-Price, Richard Ross, Neil Wright
A novel non-invasive Short Synacthen Test validated in a healthy paediatric population
Charlotte Elder, Ruben Vilela, Trevor Johnson, E Helen Kemp, Brian Keevil, John Newell-Price, Richard Ross, Neil Wright
FC1.2
Long-term effects of prenatal dexamethasone treatment and postnatal glucocorticoid treatment on brain structure in the context of CAH
Annelies van't Westeinde, Leif Karlsson, Malin Sandberg, Anna Nordenström, Nelly Paddila, Svetlana Lajic
Long-term effects of prenatal dexamethasone treatment and postnatal glucocorticoid treatment on brain structure in the context of CAH
Annelies van't Westeinde, Leif Karlsson, Malin Sandberg, Anna Nordenström, Nelly Paddila, Svetlana Lajic
FC1.3
Targetting the binding of ACTH to the Melanocortin receptor by structure modeling and design of peptide antagonists to block excess androgens in 21-hydroxylase deficiency
Shaheena Parween, Christa E Flück, Amit V Pandey
Targetting the binding of ACTH to the Melanocortin receptor by structure modeling and design of peptide antagonists to block excess androgens in 21-hydroxylase deficiency
Shaheena Parween, Christa E Flück, Amit V Pandey
FC1.4
Whole Exome Sequencing in patients with Primary Generalized Glucocorticoid Resistance identifies a novel TRIM28 gene mutation (p.R230X)
AMALIA SERTEDAKI, Nikos Marinakis, Nicolas C. Nicolaides, George Crousos, Evangelia Charmandari
Whole Exome Sequencing in patients with Primary Generalized Glucocorticoid Resistance identifies a novel TRIM28 gene mutation (p.R230X)
AMALIA SERTEDAKI, Nikos Marinakis, Nicolas C. Nicolaides, George Crousos, Evangelia Charmandari
FC1.5
Untargeted plasma metabolomics in subjects with differences in tissue glucocorticoid sensitivity identifies a novel metabolic signature
Nicolas C. Nicolaides, Maria-Konstantina Ioannidi, Eleni Koniari, Amalia Sertedaki, Maria I. Klapa, George P. Chrousos, Evangelia Charmandari
Untargeted plasma metabolomics in subjects with differences in tissue glucocorticoid sensitivity identifies a novel metabolic signature
Nicolas C. Nicolaides, Maria-Konstantina Ioannidi, Eleni Koniari, Amalia Sertedaki, Maria I. Klapa, George P. Chrousos, Evangelia Charmandari
FC1.6
A novel stem cell model for the Triple A Syndrome
Alexandra Rodrigues Da Costa, Shamma Qarin, Teisha Y. Bradshaw, David Watson, Rathi Prasad, Michael R. Barnes, Louise A. Metherell, J. Paul Chapple, William C. Skarnes, Helen L. Storr
A novel stem cell model for the Triple A Syndrome
Alexandra Rodrigues Da Costa, Shamma Qarin, Teisha Y. Bradshaw, David Watson, Rathi Prasad, Michael R. Barnes, Louise A. Metherell, J. Paul Chapple, William C. Skarnes, Helen L. Storr
LB-P15
A novel compound heterozygous mutation of the CYP17A1 gene is associated with rhabdomyolysis: Demonstration of combining 17α-hydroxylase/17,20-lyase deficiency
Hong Chen, Chunlin Wang, Li Liang, Qingfeng Yan
A novel compound heterozygous mutation of the CYP17A1 gene is associated with rhabdomyolysis: Demonstration of combining 17α-hydroxylase/17,20-lyase deficiency
Hong Chen, Chunlin Wang, Li Liang, Qingfeng Yan
LB-P19
Characterization and clinical course of prolactinoma in Korean adolescents
Aram Yang, Minji Im, Ari Song, Jinsup Kim, Hyung-Jin Shin, Hwan-Hee Park, Sung Yoon Cho, Dong-Kyu Jin
Characterization and clinical course of prolactinoma in Korean adolescents
Aram Yang, Minji Im, Ari Song, Jinsup Kim, Hyung-Jin Shin, Hwan-Hee Park, Sung Yoon Cho, Dong-Kyu Jin
P1-P001
Evaluation of long term metabolic effects after prenatal dexamethasone treatment in the context of CAH - the Swedish cohort
Lena Wallensteen, Leif Karlsson, Valeria Messina, Anna Nordenström, Svetlana Lajic
Evaluation of long term metabolic effects after prenatal dexamethasone treatment in the context of CAH - the Swedish cohort
Lena Wallensteen, Leif Karlsson, Valeria Messina, Anna Nordenström, Svetlana Lajic
P1-P002
Obesity and cardio-metabolic risk factors among children and adolescents with Non Classic 21-Hydroxylase Deficiency
Liat de Vries, Yael Lebenthal, Moshe Phillip, Ariel Tenenbaum, Rachel Bello
Obesity and cardio-metabolic risk factors among children and adolescents with Non Classic 21-Hydroxylase Deficiency
Liat de Vries, Yael Lebenthal, Moshe Phillip, Ariel Tenenbaum, Rachel Bello
P1-P003
Cognition in children with congenital adrenal hyperplasia
Valeria Messina, Leif Karlsson, Tatja Hirvikoski, Anna Nordenström, Svetlana Lajic
Cognition in children with congenital adrenal hyperplasia
Valeria Messina, Leif Karlsson, Tatja Hirvikoski, Anna Nordenström, Svetlana Lajic
P1-P004
Carriers of CYP21A2 mutations have decreased mortality in infectious diseases, anational population registry study
Anna Nordenström, Johan Svensson, Svetlana Lajic, Louise Frisén, Agneta Nordenskjöld, Christina Norrby, Catarina Almqvist Malmros, Henrik Falhammar
Carriers of CYP21A2 mutations have decreased mortality in infectious diseases, anational population registry study
Anna Nordenström, Johan Svensson, Svetlana Lajic, Louise Frisén, Agneta Nordenskjöld, Christina Norrby, Catarina Almqvist Malmros, Henrik Falhammar
P1-P005
Elevated concentrations of adrenal steroid precursors with glucocorticoid activity might prevent Addisonian crisis in untreated patients with classic congenital adrenal hyperplasia
Manon Engels, Karijn Pijnenburg-Kleizen, Agustini Utari, Sultana Faradz, Joop Heuvel, Teun van Herwaarden, Paul Span, Fred Sweep, Hedi Claahsen-van der Grinten
Elevated concentrations of adrenal steroid precursors with glucocorticoid activity might prevent Addisonian crisis in untreated patients with classic congenital adrenal hyperplasia
Manon Engels, Karijn Pijnenburg-Kleizen, Agustini Utari, Sultana Faradz, Joop Heuvel, Teun van Herwaarden, Paul Span, Fred Sweep, Hedi Claahsen-van der Grinten
P1-P006
Altered DNA Methylation in peripheral T-cells from patients with Congenital Adrenal Hyperplasia
Leif Karlsson, Michela Barbaro, Ewoud Ewing, David Gomez-Cabrero, Svetlana Lajic
Altered DNA Methylation in peripheral T-cells from patients with Congenital Adrenal Hyperplasia
Leif Karlsson, Michela Barbaro, Ewoud Ewing, David Gomez-Cabrero, Svetlana Lajic
P1-P007
Birth incidence, age at diagnosis, mortality in Congenital Adrenal Hyperplasia in Korea: a Nationwide Population-based Study
Jihyun Kim, Jong Bin Lee
Birth incidence, age at diagnosis, mortality in Congenital Adrenal Hyperplasia in Korea: a Nationwide Population-based Study
Jihyun Kim, Jong Bin Lee
P1-P008
Impact of puberty on final height in children and adolescents with Congenital Adrenal Hyperplasia (CAH)
Julia Rohayem, Felix Schreiner, Stefan Riedl, Egbert Voss, Johannes Wolf, Corinna Grasemann, Katharina Fink, Klaus Mohnicke
Impact of puberty on final height in children and adolescents with Congenital Adrenal Hyperplasia (CAH)
Julia Rohayem, Felix Schreiner, Stefan Riedl, Egbert Voss, Johannes Wolf, Corinna Grasemann, Katharina Fink, Klaus Mohnicke
P1-P009
The relationship of baseline, incremental and peak cortisol following a Short Synacthen Test – single-centre analysis of three years’ data
Apoorva Aji, Sharon Colyer, Sarah Burn, Paul Dimitri, Neil Wright, Nils Krone, Charlotte Elder
The relationship of baseline, incremental and peak cortisol following a Short Synacthen Test – single-centre analysis of three years’ data
Apoorva Aji, Sharon Colyer, Sarah Burn, Paul Dimitri, Neil Wright, Nils Krone, Charlotte Elder
P1-P010
The circadian rhythm of cortisol binding globulin has little impact on cortisol exposure after hydrocortisone dosing
Johanna Melin, Niklas Hartung, Zinnia Parra-Guillen, Martin Whitaker, Richard Ross, Charlotte Kloft
The circadian rhythm of cortisol binding globulin has little impact on cortisol exposure after hydrocortisone dosing
Johanna Melin, Niklas Hartung, Zinnia Parra-Guillen, Martin Whitaker, Richard Ross, Charlotte Kloft
P1-P011
Characterizing the Steroidome in ammniotic fluid of mid-gestation by LC-MS/MS
Rong Wang, Dov Tiosano, Michaela F. Hartmann, Stefan A. Wudy
Characterizing the Steroidome in ammniotic fluid of mid-gestation by LC-MS/MS
Rong Wang, Dov Tiosano, Michaela F. Hartmann, Stefan A. Wudy
P1-P012
Pediatric Adrenocortical Tumors. A single tertiary center experience: Clinical, Biological and Pathologic Characteristics Analysis.
Maria Celeste Mattone, Silvia Gil, Maria Laura Galluzzo Mutti, Alejandra Casanovas, Juan Manuel Lazzati, Veronica Zaidman, Alicia Belgorosky, Gabriela Guercio
Pediatric Adrenocortical Tumors. A single tertiary center experience: Clinical, Biological and Pathologic Characteristics Analysis.
Maria Celeste Mattone, Silvia Gil, Maria Laura Galluzzo Mutti, Alejandra Casanovas, Juan Manuel Lazzati, Veronica Zaidman, Alicia Belgorosky, Gabriela Guercio
P1-P013
Role of mast cells in the establishment of the mineralocorticoid pathway in the developing mouse
Alexandre Naccache, Estelle Louiset, Antonin Lamaziere, Michael Thomas, Arnaud Arabo, Hervé Lefebvre, Mireille Castanet
Role of mast cells in the establishment of the mineralocorticoid pathway in the developing mouse
Alexandre Naccache, Estelle Louiset, Antonin Lamaziere, Michael Thomas, Arnaud Arabo, Hervé Lefebvre, Mireille Castanet
P1-P014
Molecular characterization of TNXA/TNXB chimeras in CYP21A2 gene deletions: high frequency of undiagnosed Ehlers-Danlos syndrome in Congenital Adrenal Hyperplasia patients
Roxana Marino, Guillermo Notaristéfano, Natalia Perez Garrido, Pablo Ramirez, Maria Sol Touzon, Matías Pujana, Angélica Moresco, Gabriela Finkielstain, Gabriela Obregón, Marco A Rivarola, Alicia Belgorosky
Molecular characterization of TNXA/TNXB chimeras in CYP21A2 gene deletions: high frequency of undiagnosed Ehlers-Danlos syndrome in Congenital Adrenal Hyperplasia patients
Roxana Marino, Guillermo Notaristéfano, Natalia Perez Garrido, Pablo Ramirez, Maria Sol Touzon, Matías Pujana, Angélica Moresco, Gabriela Finkielstain, Gabriela Obregón, Marco A Rivarola, Alicia Belgorosky
P1-P015
New insights into Low Dose Dexamethasone Suppression Test in paediatric Cushing’s Syndrome (CS)
Ingrid C.E. Wilkinson, Lee Martin, Ashley B. Grossman, John P. Monson, Scott Akker, Martin O. Savage, William M. Drake, Helen L. Storr
New insights into Low Dose Dexamethasone Suppression Test in paediatric Cushing’s Syndrome (CS)
Ingrid C.E. Wilkinson, Lee Martin, Ashley B. Grossman, John P. Monson, Scott Akker, Martin O. Savage, William M. Drake, Helen L. Storr
P1-P016
Recurrent hypoglycemia in a preschooler girl with overgrowth: Isolated ACTH-deficiency with a novel TPIT mutation
Zehra Yavas Abali, Gozde Yesil, Tarik Kirkgoz, Sare Betul Kaygusuz, Serap Turan, Abdullah Bereket, Tulay Guran
Recurrent hypoglycemia in a preschooler girl with overgrowth: Isolated ACTH-deficiency with a novel TPIT mutation
Zehra Yavas Abali, Gozde Yesil, Tarik Kirkgoz, Sare Betul Kaygusuz, Serap Turan, Abdullah Bereket, Tulay Guran
P1-P017
Biochemical, genetic and molecular characterization of a novel P399_E401Dup mutation in P450 oxidoreductase (POR) altering several enzymatic activities in a patient with a 46,XX DSD phenotype at birth
Claudia Boettcher, Shaheena Parween, Eckhard Korsch, Michaela F Hartmann, Sameer Udhane, Norio Kagawa, Christa E Flück, Stefan A Wudy, Amit V Pandey
Biochemical, genetic and molecular characterization of a novel P399_E401Dup mutation in P450 oxidoreductase (POR) altering several enzymatic activities in a patient with a 46,XX DSD phenotype at birth
Claudia Boettcher, Shaheena Parween, Eckhard Korsch, Michaela F Hartmann, Sameer Udhane, Norio Kagawa, Christa E Flück, Stefan A Wudy, Amit V Pandey
P1-P018
Young lean women with evidence of both premature adrenarche and pubarche display a metabolic, hormonal and psychologic profile that is similar to that of their peers with polycystic ovary syndrome
Sarantis Livadas, Christina Bothou, Christina Kanaka-Gantenbein, Dimitrios Chiotis, Nicholas Angelopoulos, Djuro Macut, George P Chrousos
Young lean women with evidence of both premature adrenarche and pubarche display a metabolic, hormonal and psychologic profile that is similar to that of their peers with polycystic ovary syndrome
Sarantis Livadas, Christina Bothou, Christina Kanaka-Gantenbein, Dimitrios Chiotis, Nicholas Angelopoulos, Djuro Macut, George P Chrousos
P1-P019
The usefulness of combined analysis of serum and salivary maximum cortisol response to low-dose ACTH test to define the requirement of hormone replacement treatment.
Elisa Vaiani, Juan Manuel Lazzati, Mercedes Maceiras, Silvia Gil, Mariana Costanzo, Veronica Zaidman, Gustavo Dratler, Alicia Belgorosky
The usefulness of combined analysis of serum and salivary maximum cortisol response to low-dose ACTH test to define the requirement of hormone replacement treatment.
Elisa Vaiani, Juan Manuel Lazzati, Mercedes Maceiras, Silvia Gil, Mariana Costanzo, Veronica Zaidman, Gustavo Dratler, Alicia Belgorosky
P1-P020
High DHEAS (HD) in girls determines earlier pubertal maturation and mild hyperandrogenism throughout pubertal development
Ana Pereira, Paulina Merino, German Iñiguez, Camila Corvalan, Veronica Mericq
High DHEAS (HD) in girls determines earlier pubertal maturation and mild hyperandrogenism throughout pubertal development
Ana Pereira, Paulina Merino, German Iñiguez, Camila Corvalan, Veronica Mericq
P1-P021
Higher Dehydroepiandrosterone levels in prepubertal children born very preterm
Veronica Mericq, Alejandro Martinez-Aguayo, German Iñiguez, Helena Poggi, Ivonne D'Apremont, Rosario Moore, Monica Arancibia, Hernan Garcia, Soledad Peredo, Claudia Trincado, Sofia Sifaqui, Jose Tomas Ossa, Carlos Fardella, Cristian Carvajal, Carmen Campino, Rene Baudrand, Sandra Solari, Fidel Allende
Higher Dehydroepiandrosterone levels in prepubertal children born very preterm
Veronica Mericq, Alejandro Martinez-Aguayo, German Iñiguez, Helena Poggi, Ivonne D'Apremont, Rosario Moore, Monica Arancibia, Hernan Garcia, Soledad Peredo, Claudia Trincado, Sofia Sifaqui, Jose Tomas Ossa, Carlos Fardella, Cristian Carvajal, Carmen Campino, Rene Baudrand, Sandra Solari, Fidel Allende
P1-P022
A large consanguineous family with a mild and transient form of autosomal recessive Pseudohypoaldosteronism type 1 (PHA1) caused by a novel mutation in the SCNN1A gene: functional studies
Alexandra Efthymiadou, I Gautschi, M.X vanBemmelen, Amalia Sertedaki, George Chrousos, Laurent Schild, Dionisios Chrysis
A large consanguineous family with a mild and transient form of autosomal recessive Pseudohypoaldosteronism type 1 (PHA1) caused by a novel mutation in the SCNN1A gene: functional studies
Alexandra Efthymiadou, I Gautschi, M.X vanBemmelen, Amalia Sertedaki, George Chrousos, Laurent Schild, Dionisios Chrysis
P1-P023
Associations between maternal and offspring hair cortisol concentrations and child behavioral symptoms in pairs of children 18-48 months old and their mothers with and without perinatal mental disorders
Anna Agapaki, Fenia Papagianni, Eleni Valavani, Ioannis Zervas, Aimilia Mantziou, Stamatina Kanelli, Areti Spyropoulou, George Chrousos, Panagiota Pervanidou
Associations between maternal and offspring hair cortisol concentrations and child behavioral symptoms in pairs of children 18-48 months old and their mothers with and without perinatal mental disorders
Anna Agapaki, Fenia Papagianni, Eleni Valavani, Ioannis Zervas, Aimilia Mantziou, Stamatina Kanelli, Areti Spyropoulou, George Chrousos, Panagiota Pervanidou
P1-P024
Gonadotropin-Dependent Pubertal Disorders are Common in Patients with Virilizing Adrenocortical Tumors in Childhood
Monica F. Stecchini, Zilda Braid, Candy B. More, Davi C. Aragon, Margaret Castro, Ayrton C. Moreira, Sonir R. Antonini
Gonadotropin-Dependent Pubertal Disorders are Common in Patients with Virilizing Adrenocortical Tumors in Childhood
Monica F. Stecchini, Zilda Braid, Candy B. More, Davi C. Aragon, Margaret Castro, Ayrton C. Moreira, Sonir R. Antonini
P2-P001
Contribution of direct measurements of steroids by liquid chromatography tandem mass spectrometry (LC-MS/MS) in non-classical adrenal hyperplasia (NCCAH)
Helena Agnani, Muriel HOUANG, Thibaut EGETHER, Irène Netchine, Antonin LAMAZIERE
Contribution of direct measurements of steroids by liquid chromatography tandem mass spectrometry (LC-MS/MS) in non-classical adrenal hyperplasia (NCCAH)
Helena Agnani, Muriel HOUANG, Thibaut EGETHER, Irène Netchine, Antonin LAMAZIERE
P2-P002
GnRH-analogue treatment in children with congenital adrenal hyperplasia (CAH): data from a multicenter CAH registry
Felix Schreiner, Julia Rohayem, Susanne Fricke-Otto, Sven Golembowski, Norbert Jorch, Karl Otfried Schwab, Katharina Warncke, Ulrike Zanier, . on behalf of the German CAH registry (DGKED-QS)
GnRH-analogue treatment in children with congenital adrenal hyperplasia (CAH): data from a multicenter CAH registry
Felix Schreiner, Julia Rohayem, Susanne Fricke-Otto, Sven Golembowski, Norbert Jorch, Karl Otfried Schwab, Katharina Warncke, Ulrike Zanier, . on behalf of the German CAH registry (DGKED-QS)
P2-P003
Glucocorticoid replacement regimens in the treatment of 21-hydroxylase deficiency congenital adrenal hyperplasia: a systematic Cochrane review
Sze Ng, Karolina Stepien
Glucocorticoid replacement regimens in the treatment of 21-hydroxylase deficiency congenital adrenal hyperplasia: a systematic Cochrane review
Sze Ng, Karolina Stepien
P2-P004
Hydrocortisone (HC) dose in children with congenital adrenal hyperplasia (CAH)
Heike Hoyer-Kuhn, Angela Huebner, Annette Richter-Unruh, Rudolf Oeverink, Markus Bettendorf, Tilman Rohrer, Klaus Kapelari, Friedrich-Wilhelm Roehl, Reinhard Holl, Joachim Woelfle, on behalf of the German CAH registry
Hydrocortisone (HC) dose in children with congenital adrenal hyperplasia (CAH)
Heike Hoyer-Kuhn, Angela Huebner, Annette Richter-Unruh, Rudolf Oeverink, Markus Bettendorf, Tilman Rohrer, Klaus Kapelari, Friedrich-Wilhelm Roehl, Reinhard Holl, Joachim Woelfle, on behalf of the German CAH registry
P2-P005
Perioperative care of CAH – Incongruencies of Practices among Canadian Specialists
Munier Nour, Hardave Gill, Prosanta Mondal, Mark Inman, Kristine Urmson
Perioperative care of CAH – Incongruencies of Practices among Canadian Specialists
Munier Nour, Hardave Gill, Prosanta Mondal, Mark Inman, Kristine Urmson
P2-P006
Analysis of phenotypes and genotypes in 84 patients with 21-hydroxylase deficiency
Lele Hou, Shaofen Lin, Zhe Meng, Hui Ou, Zulin Liu, Lina Zhang, Zhuannan Jiang, Liyang Liang
Analysis of phenotypes and genotypes in 84 patients with 21-hydroxylase deficiency
Lele Hou, Shaofen Lin, Zhe Meng, Hui Ou, Zulin Liu, Lina Zhang, Zhuannan Jiang, Liyang Liang
P2-P007
Miscarriages in families with a child with classic congenital adrenal hyperplasia and 21-hydroxylase deficiency (CAH)
Theresa Penger, Johannes Hess, Michaela Marx, Patricia Oppelt, Helmuth-Günther Dörr
Miscarriages in families with a child with classic congenital adrenal hyperplasia and 21-hydroxylase deficiency (CAH)
Theresa Penger, Johannes Hess, Michaela Marx, Patricia Oppelt, Helmuth-Günther Dörr
P2-P008
Testing antiandrogens and aromatase inhibitors to achieve normal growth in children with classical congenital adrenal hyperplasia:a systematic review and meta-analysis
Rana Al Balwi, Wedad Al madani, Rania Saad, Mazen Ferwana
Testing antiandrogens and aromatase inhibitors to achieve normal growth in children with classical congenital adrenal hyperplasia:a systematic review and meta-analysis
Rana Al Balwi, Wedad Al madani, Rania Saad, Mazen Ferwana
P2-P009
Phenotype-genotype correlations of CYP21A2 mutations in patients with Congenital Adrenal Hyperplasia in Turkey
Enver Simsek, Cigdem Binay, Oguz Cilingir, Meliha Demiral, Ilhan Hazer, Sevilhan Artan
Phenotype-genotype correlations of CYP21A2 mutations in patients with Congenital Adrenal Hyperplasia in Turkey
Enver Simsek, Cigdem Binay, Oguz Cilingir, Meliha Demiral, Ilhan Hazer, Sevilhan Artan
P2-P010
Hypoglycemic crisis and salt loss in children with classic congenital adrenal hyperplasia
Simona Badalucco, Silvia Laura Carla Meroni, Alessandra Di Lascio, Moira Gianninoto, Marianna Rita Stancampiano, Gianni Russo
Hypoglycemic crisis and salt loss in children with classic congenital adrenal hyperplasia
Simona Badalucco, Silvia Laura Carla Meroni, Alessandra Di Lascio, Moira Gianninoto, Marianna Rita Stancampiano, Gianni Russo
P2-P011
Neonatal screening for congenital adrenal hyperplasia in Turkey: a pilot study with 38,935 infants
Tulay Guran, Basak Tezel, Fatih Gurbuz, Beray Selver Eklioglu, Nihal Hatipoglu, Cengiz Kara, Nuran Sahin, Enver Simsek, Filiz Mine Cizmecioglu, Alev Ozon, Firdevs Bas, Murat Aydin, Gulsum Ozdemir, Feyza Darendeliler
Neonatal screening for congenital adrenal hyperplasia in Turkey: a pilot study with 38,935 infants
Tulay Guran, Basak Tezel, Fatih Gurbuz, Beray Selver Eklioglu, Nihal Hatipoglu, Cengiz Kara, Nuran Sahin, Enver Simsek, Filiz Mine Cizmecioglu, Alev Ozon, Firdevs Bas, Murat Aydin, Gulsum Ozdemir, Feyza Darendeliler
P2-P012
Autoantibodies against 21-hydroxylase in prediction of adrenal failure in APECED patients.
Leila Sozaeva, Nadezhda Makazan, Larisa Nikankina, Maria Kareva, Elizaveta Orlova, Valentina Peterkova
Autoantibodies against 21-hydroxylase in prediction of adrenal failure in APECED patients.
Leila Sozaeva, Nadezhda Makazan, Larisa Nikankina, Maria Kareva, Elizaveta Orlova, Valentina Peterkova
P2-P013
A first combination case of 21-hydroxilase deficiency and CHARGE syndrome confirmed by genetic analysis
Miyuki Kitamura, Yuko Katoh-Fukui, Maki Fukami, Shuichi Yatsuga, Takako Matsumoto, Junko Nishioka, Yasutoshi Koga
A first combination case of 21-hydroxilase deficiency and CHARGE syndrome confirmed by genetic analysis
Miyuki Kitamura, Yuko Katoh-Fukui, Maki Fukami, Shuichi Yatsuga, Takako Matsumoto, Junko Nishioka, Yasutoshi Koga
P2-P014
Frequency of Enzyme Deficiencies in a Turkish Cohort of Congenital Adrenal Hyperplasia: A Single-Center Experience with 145 Patients
Melek Yildiz, Hasan Onal, Banu Aydin, Abdurrahman Akgun, Beyza Belde Dogan, Neval Topal, Teoman Akcay, Erdal Adal
Frequency of Enzyme Deficiencies in a Turkish Cohort of Congenital Adrenal Hyperplasia: A Single-Center Experience with 145 Patients
Melek Yildiz, Hasan Onal, Banu Aydin, Abdurrahman Akgun, Beyza Belde Dogan, Neval Topal, Teoman Akcay, Erdal Adal
P2-P015
Study of cardiovascular risk factors and carotid intima-media thickness in children with Congenital Adrenal Hyperplasia
Shaymaa Elsayed, Mohamed Emam, Magdy Abd El Fattah, Ahmed Abou Gabal
Study of cardiovascular risk factors and carotid intima-media thickness in children with Congenital Adrenal Hyperplasia
Shaymaa Elsayed, Mohamed Emam, Magdy Abd El Fattah, Ahmed Abou Gabal
P2-P016
The spectrum of genetic defects in Congenital Adrenal Hyperplasia in the population of Cyprus: a retrospective analysis
Nicos Skordis, Pavlos Fanis, Meropi Toumba, Charilaos Stylianou, Michalis Picolos, Elena Andreou, Andreas Kyriakou, Lambrini Yiannakide-Myli, Michalis Iasonides, Stella Nicolaou, Tassos C Kyriakides, George A Tanteles, Vassos Neocleous, Leonidas A Phylactou
The spectrum of genetic defects in Congenital Adrenal Hyperplasia in the population of Cyprus: a retrospective analysis
Nicos Skordis, Pavlos Fanis, Meropi Toumba, Charilaos Stylianou, Michalis Picolos, Elena Andreou, Andreas Kyriakou, Lambrini Yiannakide-Myli, Michalis Iasonides, Stella Nicolaou, Tassos C Kyriakides, George A Tanteles, Vassos Neocleous, Leonidas A Phylactou
P2-P017
Childhood growth advancement in girls with premature adrenarche heralds anabolic effects by adulthood
Jani Liimatta, Pauliina Utriainen, Tomi Laitinen, Raimo Voutilainen, Jarmo Jääskeläinen
Childhood growth advancement in girls with premature adrenarche heralds anabolic effects by adulthood
Jani Liimatta, Pauliina Utriainen, Tomi Laitinen, Raimo Voutilainen, Jarmo Jääskeläinen
P2-P018
A novel mutation in the MC2R gene in a two-year-old boy with adrenal insufficiency
Sara Al-Khawaga, Khalid Hussain*
A novel mutation in the MC2R gene in a two-year-old boy with adrenal insufficiency
Sara Al-Khawaga, Khalid Hussain*
P2-P019
Two cases of apparent mineralocorticoid excess due to novel mutations in HSD11B2 gene
Nina Makretskaya, Irina Kostrova, Anatoly Tiulpakov
Two cases of apparent mineralocorticoid excess due to novel mutations in HSD11B2 gene
Nina Makretskaya, Irina Kostrova, Anatoly Tiulpakov
P2-P020
Long-term follow-up of safety and disease control for hydrocortisone granules designed to give age-appropriate dosing with taste masking to children with adrenal insufficiency
Uta Neumann, Katarina Braune, Martin Whitaker, Susanna Wiegand, Heiko Krude, John Porter, Dena Digweed, Bernard Voet, Richard Ross, Madhu Davies, Oliver Blankenstein
Long-term follow-up of safety and disease control for hydrocortisone granules designed to give age-appropriate dosing with taste masking to children with adrenal insufficiency
Uta Neumann, Katarina Braune, Martin Whitaker, Susanna Wiegand, Heiko Krude, John Porter, Dena Digweed, Bernard Voet, Richard Ross, Madhu Davies, Oliver Blankenstein
P2-P021
Borderline peak plasma cortisol following Synacthen stimulation – single-centre analysis of three years’ data
Sarah Burn, Sharon Colyer, Paul Dimitri, Neil Wright, Nils Krone, Charlotte Elder
Borderline peak plasma cortisol following Synacthen stimulation – single-centre analysis of three years’ data
Sarah Burn, Sharon Colyer, Paul Dimitri, Neil Wright, Nils Krone, Charlotte Elder
P2-P022
Unilateral Adrenalectomy for primary pigmented nodular adrenocortical disease causing Cushing Syndrome
Shinji Higuchi, Rie Kawakita, Yuki Hosokawa, Yuki Yamada, Maki Oyachi, Kana Matsumura, Tohru Yorifuji
Unilateral Adrenalectomy for primary pigmented nodular adrenocortical disease causing Cushing Syndrome
Shinji Higuchi, Rie Kawakita, Yuki Hosokawa, Yuki Yamada, Maki Oyachi, Kana Matsumura, Tohru Yorifuji
P2-P023
Adrenal crisis in children with adrenal insufficiency: prevalence and risk factors
Ori Eyal, Yair Levin, Asaf Oren, Amnon Zung, Marianna Rachmiel, Zohar Landau, Naomi Weintrob
Adrenal crisis in children with adrenal insufficiency: prevalence and risk factors
Ori Eyal, Yair Levin, Asaf Oren, Amnon Zung, Marianna Rachmiel, Zohar Landau, Naomi Weintrob
P2-P024
The effectiveness of a Stress-Management Intervention Program in behavioral parameters and hair cortisol concentrations in children with Attention Deficit Hyperactivity Disorder
August Kapogiannis, Gerasimos Makris, Aimilia Mantzou, Theodora Bachourou, Christina Darviri, George Chrousos, Panagiota Pervanidou
The effectiveness of a Stress-Management Intervention Program in behavioral parameters and hair cortisol concentrations in children with Attention Deficit Hyperactivity Disorder
August Kapogiannis, Gerasimos Makris, Aimilia Mantzou, Theodora Bachourou, Christina Darviri, George Chrousos, Panagiota Pervanidou
P2-P025
Very high dehydroepiandrosterone sulfate (DHEAS) in serum of an overweight female adolescent without a tumor
Daniel Iliev, Regina Braun, Alberto Sànchez-Guijo, Stefan Wudy, Doreen Heckmann, Gernot Bruchelt, Anika Rösner, Gary Grosser, Joachim Geyer, Gerhard Binder
Very high dehydroepiandrosterone sulfate (DHEAS) in serum of an overweight female adolescent without a tumor
Daniel Iliev, Regina Braun, Alberto Sànchez-Guijo, Stefan Wudy, Doreen Heckmann, Gernot Bruchelt, Anika Rösner, Gary Grosser, Joachim Geyer, Gerhard Binder
P2-P026
Early recognition of adrenal insufficiency after hematopoietic stem cell transplantation during childhood
Yujung Choi, Seonhwa Lee, Seul ki Kim, Eun Kyoung Lee, Jung-Hyun Shin, Moon Bae Ahn, Won-Kyoung Cho, Min-Ho Jung, Byung-Kyu Suh
Early recognition of adrenal insufficiency after hematopoietic stem cell transplantation during childhood
Yujung Choi, Seonhwa Lee, Seul ki Kim, Eun Kyoung Lee, Jung-Hyun Shin, Moon Bae Ahn, Won-Kyoung Cho, Min-Ho Jung, Byung-Kyu Suh
P2-P027
Reference values for serum 17-alfa hydroxyprogesterone and adrenal size in healthy newborns
Gülay Karagüzel, İlker Eyüboğlu, Sebahat Özdem, Şebnem Kader, Serpil Kaya, Ercüment Beyhun
Reference values for serum 17-alfa hydroxyprogesterone and adrenal size in healthy newborns
Gülay Karagüzel, İlker Eyüboğlu, Sebahat Özdem, Şebnem Kader, Serpil Kaya, Ercüment Beyhun
P2-P028
A rare case of ACTH- independent Cushing’s syndrome due to bilateral micronodular adrenal hyperplasia and myoclonic dystonia
Ioannis- Anargyros Vasilakis, Paraskevi Kazakou, Christina Kogia, Maria Karaflou, George Chrousos, Evangelia Charmandari
A rare case of ACTH- independent Cushing’s syndrome due to bilateral micronodular adrenal hyperplasia and myoclonic dystonia
Ioannis- Anargyros Vasilakis, Paraskevi Kazakou, Christina Kogia, Maria Karaflou, George Chrousos, Evangelia Charmandari
P2-P029
Two siblins and three cousins with Allgrove (4A) syndrome in a Turkısh family:a novel mutation in the 'aladin' gene
Aysehan Akinci, Ismail Dundar, Emine Camtosun, Leman Kayas
Two siblins and three cousins with Allgrove (4A) syndrome in a Turkısh family:a novel mutation in the 'aladin' gene
Aysehan Akinci, Ismail Dundar, Emine Camtosun, Leman Kayas
P2-P030
Ganglioneuroma presenting as an adrenal incidentaloma in a 10-year-old boy-a rare entity
Meghna Chawla, Tushar Deshpande
Ganglioneuroma presenting as an adrenal incidentaloma in a 10-year-old boy-a rare entity
Meghna Chawla, Tushar Deshpande
P2-P031
The relationship between vitamin D status and metabolic abnormalities in females with classical Congenital Adrenal Hyperplasia: a pilot study
Mona Hassan, Amany Ibrahim, Marise Abdou, Sahar Abdel Atty, Diana Nabil
The relationship between vitamin D status and metabolic abnormalities in females with classical Congenital Adrenal Hyperplasia: a pilot study
Mona Hassan, Amany Ibrahim, Marise Abdou, Sahar Abdel Atty, Diana Nabil
P2-P032
Adrenal hypoplasia seemingly first as a primary hypoaldosteronism
Lorenzo Iughetti, Laura Lucaccioni, Patrizia Bruzzi, Silvia Ciancia, Barbara Predieri, Florence Roucher-Boulez
Adrenal hypoplasia seemingly first as a primary hypoaldosteronism
Lorenzo Iughetti, Laura Lucaccioni, Patrizia Bruzzi, Silvia Ciancia, Barbara Predieri, Florence Roucher-Boulez
P2-P033
Quantitative ultrasound evaluation in a cohort of 43 young adults with classical CAH due to 21-hydroxylase deficiency (21OHD): is bone mineral quality impaired?
Federico Baronio, Antonio Balsamo, Rita Ortolano, Nicoletta Massaccesi, Ilaria Bettocchi, Maximiliano Zioutas, Giulio Maltoni, Stefano Zucchini, Alessandra Cassio
Quantitative ultrasound evaluation in a cohort of 43 young adults with classical CAH due to 21-hydroxylase deficiency (21OHD): is bone mineral quality impaired?
Federico Baronio, Antonio Balsamo, Rita Ortolano, Nicoletta Massaccesi, Ilaria Bettocchi, Maximiliano Zioutas, Giulio Maltoni, Stefano Zucchini, Alessandra Cassio
P2-P034
Etiology of Primary Adrenal Insufficiency in children:a 29-year single center experience
Huamei MA, Jun ZHANG, Song GUO, Yanhong LI, Hongshan CHEN, Qiu CHEN, Minlian DU, Shaofu LI
Etiology of Primary Adrenal Insufficiency in children:a 29-year single center experience
Huamei MA, Jun ZHANG, Song GUO, Yanhong LI, Hongshan CHEN, Qiu CHEN, Minlian DU, Shaofu LI
P2-P035
Pseudopubertas praecox in a 4 year old boy with bilateral atypical adrenocortical adenomas
Corinna Brichta, Michael Wurm, Franka Hodde, Natascha van der Werf-Grohmann, Karl Otfried Schwab
Pseudopubertas praecox in a 4 year old boy with bilateral atypical adrenocortical adenomas
Corinna Brichta, Michael Wurm, Franka Hodde, Natascha van der Werf-Grohmann, Karl Otfried Schwab
P3-P003
Nelson’s syndrome after bilateral adrenalectomy for Cushing’s Disease in pediatric age – report of a case
Catarina M. Machado, Ana L. Leite, Ana Sousa, Lúcia Almeida, Rosa Arménia Campos, Maria João Oliveira, Jorge Sales Marques
Nelson’s syndrome after bilateral adrenalectomy for Cushing’s Disease in pediatric age – report of a case
Catarina M. Machado, Ana L. Leite, Ana Sousa, Lúcia Almeida, Rosa Arménia Campos, Maria João Oliveira, Jorge Sales Marques
P3-P004
Basal levels of 17-hydroxyprogesterone can distinguish isolated precocious pubarche from non-classical congenital adrenal hyperplasia in children: a prospective observational study
anna grandone, Adalgisa Festa, Michela Mariani, Caterina Luongo, Emanuele Miraglia del Giudice
Basal levels of 17-hydroxyprogesterone can distinguish isolated precocious pubarche from non-classical congenital adrenal hyperplasia in children: a prospective observational study
anna grandone, Adalgisa Festa, Michela Mariani, Caterina Luongo, Emanuele Miraglia del Giudice
P3-P005
Age at diagnosis and outcome in Maghreb patients with 21-hydroxylase deficient congenital adrenal hyperplasia; urgent need for newborn screening
Asmahane Ladjouze, Imane Yala, Manel Yahiaoui, Dounia Zerguini, Veronique Tardy, Kahina Mohammedi, Ourida N Taleb, Soraya Kerkouche, Karima Berkouk, Manoubia Bensmina, Abdeljlil Maoudj, Rawda Aboura, Tahar Anane, Yves Morel, Zahir Bouzerar
Age at diagnosis and outcome in Maghreb patients with 21-hydroxylase deficient congenital adrenal hyperplasia; urgent need for newborn screening
Asmahane Ladjouze, Imane Yala, Manel Yahiaoui, Dounia Zerguini, Veronique Tardy, Kahina Mohammedi, Ourida N Taleb, Soraya Kerkouche, Karima Berkouk, Manoubia Bensmina, Abdeljlil Maoudj, Rawda Aboura, Tahar Anane, Yves Morel, Zahir Bouzerar
P3-P006
An adrenal tumor presenting as a premature pubarche in a 7 year-old girl.
CAMPAS-LEBECQUE Marie-Neige, SOUTO Isabelle, PROUST Stéphanie, LECLAIR Marc-David, SUTEAU Valentine, BAILLEUL Justine, AZGAL Maryam, BOUHOURS-NOUET Natacha, COUTANT Régis
An adrenal tumor presenting as a premature pubarche in a 7 year-old girl.
CAMPAS-LEBECQUE Marie-Neige, SOUTO Isabelle, PROUST Stéphanie, LECLAIR Marc-David, SUTEAU Valentine, BAILLEUL Justine, AZGAL Maryam, BOUHOURS-NOUET Natacha, COUTANT Régis
P3-P007
Refractory Cyclical Cushing's Disease -a case of multiple pituitary micro-adenomas in a three year old girl after 8 years follow up
Elizabeth Robinson, Poonam Dharmaraj Poonam, Carl van Heyningen
Refractory Cyclical Cushing's Disease -a case of multiple pituitary micro-adenomas in a three year old girl after 8 years follow up
Elizabeth Robinson, Poonam Dharmaraj Poonam, Carl van Heyningen
P3-P009
Early diagnosis of Duchenne muscular dystrophy in 6-months-old male with primary adrenal insufficiency
Eda Yanar, Irina Kopylova, Ilya Kanivets, Sergey Korostelev, Denis Pyankov, Ekaterina Zakharova, Maria Kareva, Elizaveta Orlova
Early diagnosis of Duchenne muscular dystrophy in 6-months-old male with primary adrenal insufficiency
Eda Yanar, Irina Kopylova, Ilya Kanivets, Sergey Korostelev, Denis Pyankov, Ekaterina Zakharova, Maria Kareva, Elizaveta Orlova
P3-P010
Lipoid Adrenal Hyperplasia diagnosed with severe cholestasis in newborn
emel hatun aytaç kaplan, nuriye aslı melekoğlu, mehmet keskin, derya çağatay, kadri karaer
Lipoid Adrenal Hyperplasia diagnosed with severe cholestasis in newborn
emel hatun aytaç kaplan, nuriye aslı melekoğlu, mehmet keskin, derya çağatay, kadri karaer
P3-P011
Severe hyponatraemia with absence of hyperkalaemia in a patient with Addison's disease
Hakan Doneray, Ayse Ozden, Nagihan Erol Kizilelma
Severe hyponatraemia with absence of hyperkalaemia in a patient with Addison's disease
Hakan Doneray, Ayse Ozden, Nagihan Erol Kizilelma
P3-P012
Deep bronze skin without sun exposition in a 16-year old girl
Hildegard Jasser-Nitsche, Sabine Löffler, Elisabeth Suppan, Gudrun Weinhandl, Elke Fröhlich-Reiterer
Deep bronze skin without sun exposition in a 16-year old girl
Hildegard Jasser-Nitsche, Sabine Löffler, Elisabeth Suppan, Gudrun Weinhandl, Elke Fröhlich-Reiterer
P3-P015
A homozygous mutation c.518T>A (p.lle173Asn) of the CYP21A2 gene presenting as Non-Classical Congenital Adrenal Hyperplasia (NCAH)
Teodora Karamfilova, Iva Stoeva, Kalina Mihova, Rada Kaneva, Kaloyan Tsochev, Violeta Iotova
A homozygous mutation c.518T>A (p.lle173Asn) of the CYP21A2 gene presenting as Non-Classical Congenital Adrenal Hyperplasia (NCAH)
Teodora Karamfilova, Iva Stoeva, Kalina Mihova, Rada Kaneva, Kaloyan Tsochev, Violeta Iotova
P3-P017
Non-classic congenital adrenal hyperplasia causing alleles among adolescent girls with PCOS – genetical study
Lasma Lidaka, Gunta Lazdāne, Linda Gailīte, Iveta Dzivite-Krisane
Non-classic congenital adrenal hyperplasia causing alleles among adolescent girls with PCOS – genetical study
Lasma Lidaka, Gunta Lazdāne, Linda Gailīte, Iveta Dzivite-Krisane
P3-P018
Adequate interpretation of cortisol levels in children
Maria J. Chueca, Maria Villarreal, Carlos Andrés, Sara berrade, Teodoro Dura, Luiz-Miguel Nova, Pablo Rodriguez
Adequate interpretation of cortisol levels in children
Maria J. Chueca, Maria Villarreal, Carlos Andrés, Sara berrade, Teodoro Dura, Luiz-Miguel Nova, Pablo Rodriguez
P3-P019
Erythrocytosis as first manifestation of adrenal mass
Mariella Valenzise, Laura Cannavò, Giuseppina Zirilli, Graziella Iaria, Mario Lima
Erythrocytosis as first manifestation of adrenal mass
Mariella Valenzise, Laura Cannavò, Giuseppina Zirilli, Graziella Iaria, Mario Lima
P3-P020
A neonatal case with Familial Glucocorticoid Deficiency Type 1 having adrenal crisis in early period
Mehmet Keskin, Esat Koklu, Emel H.Aytac Kaplan, Murat Karaoglan, Kadri Karaer, Ozlem Keskin
A neonatal case with Familial Glucocorticoid Deficiency Type 1 having adrenal crisis in early period
Mehmet Keskin, Esat Koklu, Emel H.Aytac Kaplan, Murat Karaoglan, Kadri Karaer, Ozlem Keskin
P3-P021
Presenting features, clinical characteristics and follow up of familial isolated glucocorticoid deficiency (FGD) due to mutations in MC2R and MRAP genes
Mehmet Nuri Ozbek, Nezehat Doğan Karaşin, Huseyin Demirbilek, Meliha Demiral, Rıza Taner Baran, Tülay Güran
Presenting features, clinical characteristics and follow up of familial isolated glucocorticoid deficiency (FGD) due to mutations in MC2R and MRAP genes
Mehmet Nuri Ozbek, Nezehat Doğan Karaşin, Huseyin Demirbilek, Meliha Demiral, Rıza Taner Baran, Tülay Güran
P3-P022
Identification of X-linked adrenoleukodystrophy in boys presenting with adrenal insufficiency in the absence of adrenal antibodies
Michael Ryalls, Hoong-Wei Gan, Joe Biedenkapp, James Davison
Identification of X-linked adrenoleukodystrophy in boys presenting with adrenal insufficiency in the absence of adrenal antibodies
Michael Ryalls, Hoong-Wei Gan, Joe Biedenkapp, James Davison
P3-P023
Secondary hyperaldosteronism in the course of Cystic Fibrosis
Michał Erazmus, Anna Kucharska
Secondary hyperaldosteronism in the course of Cystic Fibrosis
Michał Erazmus, Anna Kucharska
P3-P024
The P30L mutation in the CYP21A2 gene in a girl with congenital adrenal hyperplasia with hidden salt loosing and central precocious puberty
Natallia Akulevich, Julia Boiko, Silvestro Mirabelli, Filippo DeLuca, Malgorzata Wasniewska
The P30L mutation in the CYP21A2 gene in a girl with congenital adrenal hyperplasia with hidden salt loosing and central precocious puberty
Natallia Akulevich, Julia Boiko, Silvestro Mirabelli, Filippo DeLuca, Malgorzata Wasniewska
P3-P025
Congenital adrenal hyperplasia due to a rare homozygous mutation R483P in the CYP21A2 gene and coexisting growth hormone deficiency
Natallia Akulevich, Yulia Makarava, Julia Boiko, Silvestro Mirabelli, Malgorzata Wasniewska, Filippo DeLuca
Congenital adrenal hyperplasia due to a rare homozygous mutation R483P in the CYP21A2 gene and coexisting growth hormone deficiency
Natallia Akulevich, Yulia Makarava, Julia Boiko, Silvestro Mirabelli, Malgorzata Wasniewska, Filippo DeLuca
P3-P026
Rare case of androgen producing tumor in 14 month old girl
Nino Kheladze, Elena Lundberg, Nino Totogashvili, Tinatin Tkeshelalashvili
Rare case of androgen producing tumor in 14 month old girl
Nino Kheladze, Elena Lundberg, Nino Totogashvili, Tinatin Tkeshelalashvili
P3-P028
Discrete virilization in girls with the classic form of congenital adrenal hyperplasia: the importance of a detailed genital examination at birth
Letícia Santos Silva Chagas, Gil Guerra-Junior, Maricilda Palandi De-Melo, Sofia Helena Valente Lemos-Marini
Discrete virilization in girls with the classic form of congenital adrenal hyperplasia: the importance of a detailed genital examination at birth
Letícia Santos Silva Chagas, Gil Guerra-Junior, Maricilda Palandi De-Melo, Sofia Helena Valente Lemos-Marini
P3-P029
A New Methodology for Early Identification of Steroid Resistant Acute Graft-Versus-Host Disease Patients
Alfred Gillio, Jennifer Krajewski, Michele Donato, Nancy Durning, Jeanette Haugh, Sarah Balboul, Steven Ghanny
A New Methodology for Early Identification of Steroid Resistant Acute Graft-Versus-Host Disease Patients
Alfred Gillio, Jennifer Krajewski, Michele Donato, Nancy Durning, Jeanette Haugh, Sarah Balboul, Steven Ghanny
P3-P030
Delayed diagnosis of a patient with Antley-Bixler Syndrome
Tarik Kirkgoz, Serpil Bas, Zehra Yavas Abali, Serap Turan, Abdullah Bereket, Tulay Guran
Delayed diagnosis of a patient with Antley-Bixler Syndrome
Tarik Kirkgoz, Serpil Bas, Zehra Yavas Abali, Serap Turan, Abdullah Bereket, Tulay Guran
P3-P404
Clinical and biochemical phenotype of aldosterone synthase deficiency
Katharina Förtsch, Carsten Döing, Stefan A. Wudy, Michaela F. Hartmann, Paul Martin Holterhus, Ertan Mayatepek, Christina Reinauer, Thomas Meissner, Sebastian Kummer
Clinical and biochemical phenotype of aldosterone synthase deficiency
Katharina Förtsch, Carsten Döing, Stefan A. Wudy, Michaela F. Hartmann, Paul Martin Holterhus, Ertan Mayatepek, Christina Reinauer, Thomas Meissner, Sebastian Kummer
P3-P414
Is the third time really a charm? The story about three brothers suffering from adrenoleukodystrophy and about HSCT being a chance to stop the unstoppable disease.
Marta Hetman, Krzysztof Kalwak, Ewa Barg
Is the third time really a charm? The story about three brothers suffering from adrenoleukodystrophy and about HSCT being a chance to stop the unstoppable disease.
Marta Hetman, Krzysztof Kalwak, Ewa Barg
RFC1.1
The relative contributions of genetic and environmental factors on cortisol metabolism at pre-, mid- and post-pubertal ages
Britt van Keulen, Conor Dolan, Ruth Andrew, Brian Walker, Dorret Boomsma, Joost Rotteveel, Martijn Finken
The relative contributions of genetic and environmental factors on cortisol metabolism at pre-, mid- and post-pubertal ages
Britt van Keulen, Conor Dolan, Ruth Andrew, Brian Walker, Dorret Boomsma, Joost Rotteveel, Martijn Finken
RFC1.2
Changes in CYP19A1 and CYP3A4 activities due to population genetic variations in human P450 Oxidoreductase
Shaheena Parween, Sameer S Udhane, Norio Kagawa, Amit V Pandey
Changes in CYP19A1 and CYP3A4 activities due to population genetic variations in human P450 Oxidoreductase
Shaheena Parween, Sameer S Udhane, Norio Kagawa, Amit V Pandey
RFC1.3
Sphingosine-1-phosphate lyase (SGPL1) deficiency is associated with mitochondrial dysfunction
Avinaash Maharaj, Teisha Bradshaw, Jack Williams, Tülay Güran, Debora Braslavsky, Britta Brügger, Lou Metherell, Rathi Prasad
Sphingosine-1-phosphate lyase (SGPL1) deficiency is associated with mitochondrial dysfunction
Avinaash Maharaj, Teisha Bradshaw, Jack Williams, Tülay Güran, Debora Braslavsky, Britta Brügger, Lou Metherell, Rathi Prasad
RFC1.4
Mass spectrometry-based assessment of childhood androgen excess in 487 consecutive patients over 5 years
Jan Idkowiak, Yasir S Elhassan, Pascoe Mannion, Karen Smith, Rachel Webster, Vrinda Saraff, Timothy G Barrett, Nick J Shaw, Nils Krone, Renuka P Dias, Melanie Kershaw, Jeremy Kirk, Ruth E Krone, Michael W O'Reilly, Wiebke Arlt
Mass spectrometry-based assessment of childhood androgen excess in 487 consecutive patients over 5 years
Jan Idkowiak, Yasir S Elhassan, Pascoe Mannion, Karen Smith, Rachel Webster, Vrinda Saraff, Timothy G Barrett, Nick J Shaw, Nils Krone, Renuka P Dias, Melanie Kershaw, Jeremy Kirk, Ruth E Krone, Michael W O'Reilly, Wiebke Arlt
RFC1.5
Quantitative urinary GC-MS based steroid analysis for treatment monitoring of adolescents and young adults with autoimmune primary adrenal insufficiency
Clemens Kamrath, Michaela F. Hartmann, Stefan A. Wudy
Quantitative urinary GC-MS based steroid analysis for treatment monitoring of adolescents and young adults with autoimmune primary adrenal insufficiency
Clemens Kamrath, Michaela F. Hartmann, Stefan A. Wudy
RFC1.6
A laboratory harmonization strategy for steroid hormone profiling by MoM-transformed, normalized reference ranges independent of age, sex and units
Alexandra E. Kulle, Dominika Zalas, Thomas Reinehr, Marek Niedziela, Christoph Borzikowsky, Francisca Pinto, Juliane Baumann, Maciej Flader, Gunter Simic-Schleicher, Halit Ilker Akkurt, Sabine Heger, Nadine Hornig, Paul-Martin Holterhus
A laboratory harmonization strategy for steroid hormone profiling by MoM-transformed, normalized reference ranges independent of age, sex and units
Alexandra E. Kulle, Dominika Zalas, Thomas Reinehr, Marek Niedziela, Christoph Borzikowsky, Francisca Pinto, Juliane Baumann, Maciej Flader, Gunter Simic-Schleicher, Halit Ilker Akkurt, Sabine Heger, Nadine Hornig, Paul-Martin Holterhus
FC10.1
Burosumab Improved Rickets, Phosphate Metabolism, and Clinical Outcomes Compared to Conventional Therapy in Children with X-Linked Hypophosphatemia (XLH) – A Randomized Controlled Phase 3 Study
Ola Nilsson, Michael P. Whyte, Erik A. Imel, Craig Munns, Anthony A. Portale, Leanne Ward, Jill H. Simmons, Raja Padidela, Noriyuki Namba, Hae Il Cheong, Meng Mao, Alison Skrinar, Chao-Yin Chen, Javier San Martin, Francis Glorieux
Burosumab Improved Rickets, Phosphate Metabolism, and Clinical Outcomes Compared to Conventional Therapy in Children with X-Linked Hypophosphatemia (XLH) – A Randomized Controlled Phase 3 Study
Ola Nilsson, Michael P. Whyte, Erik A. Imel, Craig Munns, Anthony A. Portale, Leanne Ward, Jill H. Simmons, Raja Padidela, Noriyuki Namba, Hae Il Cheong, Meng Mao, Alison Skrinar, Chao-Yin Chen, Javier San Martin, Francis Glorieux
FC11.1
Successful immune tolerance induction in the first case of neutralizing antibody mediated loss of efficacy of asfotase alfa treatment in hypophosphatasia
Gabriel Á. Martos-Moreno, Marta González-Vicent, Elena Sebastián, Jesús Argente
Successful immune tolerance induction in the first case of neutralizing antibody mediated loss of efficacy of asfotase alfa treatment in hypophosphatasia
Gabriel Á. Martos-Moreno, Marta González-Vicent, Elena Sebastián, Jesús Argente
FC11.2
Elevated phosphate levels inhibit skeletal muscle cell differentiation in vitro
Adalbert Raimann, Monika Egerbacher, Susanne Greber-Platzer, Alexander Dangl, Peter Pietschmann, Gabriele Haeusler
Elevated phosphate levels inhibit skeletal muscle cell differentiation in vitro
Adalbert Raimann, Monika Egerbacher, Susanne Greber-Platzer, Alexander Dangl, Peter Pietschmann, Gabriele Haeusler
FC11.3
Evidence for effects of FGF2 aptamer in an achondroplasia mice model and an in vitrochondrocyte differentiation system using patient-derived iPS cells
Keiichi Ozono, Kie Yasuda, Takeshi Kimura, Yukako Nakano, Yasuji Kitabatake, Takuo Kubota, Yosuke Nonaka, Masatoshi Fujiwara, Yoshikazu Nakamura
Evidence for effects of FGF2 aptamer in an achondroplasia mice model and an in vitrochondrocyte differentiation system using patient-derived iPS cells
Keiichi Ozono, Kie Yasuda, Takeshi Kimura, Yukako Nakano, Yasuji Kitabatake, Takuo Kubota, Yosuke Nonaka, Masatoshi Fujiwara, Yoshikazu Nakamura
FC11.4
Using patient derived induced pluripotent stem cells to model multiple epiphyseal dysplasia
Steven Woods, Peter Harley, Jamie Soul, Ni Kamprom, Nicola Bates, Qi Wang, Geert Mortier, Tim Hardingham, Susan Kimber
Using patient derived induced pluripotent stem cells to model multiple epiphyseal dysplasia
Steven Woods, Peter Harley, Jamie Soul, Ni Kamprom, Nicola Bates, Qi Wang, Geert Mortier, Tim Hardingham, Susan Kimber
FC11.5
A recurrent 6-bp intronic deletion in NESP55 with reduced penetrance in pseudohypoparathyroidism type 1b
Dong Li, Hakon Hakonarson, Michael Levine
A recurrent 6-bp intronic deletion in NESP55 with reduced penetrance in pseudohypoparathyroidism type 1b
Dong Li, Hakon Hakonarson, Michael Levine
FC11.6
Management of severe, protracted hypocalcaemia in patients undergoing thymus transplantation in a tertiary centre: a 10-year experience.
Nicole Goff, Harshini Katugampola, Elena Monti, Katherine Taylor, Rakesh Amin, Peter Hindmarsh, Catherine Peters, Shah Pratik, Helen Spoudeas, Mehul Dattani, Jeremy Allgrove, Caroline Brain
Management of severe, protracted hypocalcaemia in patients undergoing thymus transplantation in a tertiary centre: a 10-year experience.
Nicole Goff, Harshini Katugampola, Elena Monti, Katherine Taylor, Rakesh Amin, Peter Hindmarsh, Catherine Peters, Shah Pratik, Helen Spoudeas, Mehul Dattani, Jeremy Allgrove, Caroline Brain
FC2.1
Burosumab, a fully human anti-FGF23 Monoclonal Antibody, for X-linked Hypophosphatemia (XLH): sustained improvement in two Phase 2 Trials in affected children 1-12 years old
Agnès Linglart, William van't Hoff, Michael P. Whyte, Erik Imel, Anthony A. Portale, Annemieke Boot, Wolfgang Högler, Raja Padidela, Meng Mao, Alison Skrinar, Javier San Martin, Thomas O. Carpenter
Burosumab, a fully human anti-FGF23 Monoclonal Antibody, for X-linked Hypophosphatemia (XLH): sustained improvement in two Phase 2 Trials in affected children 1-12 years old
Agnès Linglart, William van't Hoff, Michael P. Whyte, Erik Imel, Anthony A. Portale, Annemieke Boot, Wolfgang Högler, Raja Padidela, Meng Mao, Alison Skrinar, Javier San Martin, Thomas O. Carpenter
FC2.2
Whole genome sequencing reveals novel intragenic deletions of GNAS as causes of pseudohypoparathyroidism type 1a
Dong Li, Caleb Bupp, Hakon Hakonarson, Michael Levine
Whole genome sequencing reveals novel intragenic deletions of GNAS as causes of pseudohypoparathyroidism type 1a
Dong Li, Caleb Bupp, Hakon Hakonarson, Michael Levine
FC2.3
Clinical course of hypoparathyroidism in patients with APECED (APS1)
Saila Laakso, Daniela Tillander, Outi Mäkitie
Clinical course of hypoparathyroidism in patients with APECED (APS1)
Saila Laakso, Daniela Tillander, Outi Mäkitie
FC2.4
Diagnostic performance of artificial neural network-based TW3 skeletal maturity assessment
Xuelian Zhou, Junfen Fu, Guanping Dong, Wei Wu, Ke Huang, Yan Ni, Qiang LIN, Lanxuan Liu, Hao Ni, Can Lai
Diagnostic performance of artificial neural network-based TW3 skeletal maturity assessment
Xuelian Zhou, Junfen Fu, Guanping Dong, Wei Wu, Ke Huang, Yan Ni, Qiang LIN, Lanxuan Liu, Hao Ni, Can Lai
FC2.5
Radial ESWT stimulates longitudinal bone growth in cultured rat fetal metatarsal bones
Sowmya Ramesh, Farasat Zaman, Vrisha Madhuri, Lars Sävendahl
Radial ESWT stimulates longitudinal bone growth in cultured rat fetal metatarsal bones
Sowmya Ramesh, Farasat Zaman, Vrisha Madhuri, Lars Sävendahl
FC2.6
Final height is negatively related to disease burden in Mitochondrial Disease
Rachel Boal, Yi Shiau Ng, Robert McFarland, Tim Cheetham
Final height is negatively related to disease burden in Mitochondrial Disease
Rachel Boal, Yi Shiau Ng, Robert McFarland, Tim Cheetham
P1-P025
Intrauterine Growth Restriction, Antenatal Steroids, Gestational Age and Breast Feeding Influence Bone Health in Prepubertal Children Born Preterm
NATASCIA DI IORGI, ANNALISA CALCAGNO, PAOLA DIANA, SARA NOTARNICOLA, ANNA MARIA ELSA ALLEGRI, FLAVIA NAPOLI, GIULIANA CANGEMI, MARIAGRAZIA CALEVO, LUCA RAMENGHI, MOHAMAD MAGHNIE
Intrauterine Growth Restriction, Antenatal Steroids, Gestational Age and Breast Feeding Influence Bone Health in Prepubertal Children Born Preterm
NATASCIA DI IORGI, ANNALISA CALCAGNO, PAOLA DIANA, SARA NOTARNICOLA, ANNA MARIA ELSA ALLEGRI, FLAVIA NAPOLI, GIULIANA CANGEMI, MARIAGRAZIA CALEVO, LUCA RAMENGHI, MOHAMAD MAGHNIE
P1-P026
Duration of breastfeeding and bone mineral density in childhood- a prospective study among preschool children
Mya Thway TINT, Wei Wei Pang, Rashida Farhad Vasanwala, Natarajan Padmapriya, Sharon Ng, Shu E Soh, Mary Fong-Fong Chong, Lynette Pei Chi Shek, Peter D Gluckman, Yap-Seng Chong, Keith M Godfrey, Marielle V Fortier, Johan G Eriksson, Yung Seng Lee, Cuilin Zhang, Fabian Yap
Duration of breastfeeding and bone mineral density in childhood- a prospective study among preschool children
Mya Thway TINT, Wei Wei Pang, Rashida Farhad Vasanwala, Natarajan Padmapriya, Sharon Ng, Shu E Soh, Mary Fong-Fong Chong, Lynette Pei Chi Shek, Peter D Gluckman, Yap-Seng Chong, Keith M Godfrey, Marielle V Fortier, Johan G Eriksson, Yung Seng Lee, Cuilin Zhang, Fabian Yap
P1-P028
Longitudinal study of bone mass in Swedish children treated with modified ketogenic diet
Anna Svedlund, Tove Hallböök, Per Magnusson, Jovanna Dahlgren, Diana Swolin-Eide
Longitudinal study of bone mass in Swedish children treated with modified ketogenic diet
Anna Svedlund, Tove Hallböök, Per Magnusson, Jovanna Dahlgren, Diana Swolin-Eide
P1-P029
Fracture epidemiology for children in Western Australia between 2005-2015: do we need to be concerned about bone health?
Mark Jenkins, Sophia Nimphius, Nicolas Hart, Paola Chivers, Timo Rantalainen, Kristina Rüter, Meredith Borland, Fleur McIntyre, Katherine Stannage, Aris Siafarikas
Fracture epidemiology for children in Western Australia between 2005-2015: do we need to be concerned about bone health?
Mark Jenkins, Sophia Nimphius, Nicolas Hart, Paola Chivers, Timo Rantalainen, Kristina Rüter, Meredith Borland, Fleur McIntyre, Katherine Stannage, Aris Siafarikas
P1-P030
Bone biochemistry in children with fractures presenting with suspected non-accidental injury
Owen Forbes, Jane McNeilly, Helen McDevitt, James Houston, S. Faisal Ahmed, Avril Mason
Bone biochemistry in children with fractures presenting with suspected non-accidental injury
Owen Forbes, Jane McNeilly, Helen McDevitt, James Houston, S. Faisal Ahmed, Avril Mason
P1-P031
Systematic screening using DXA Lateral Vertebral Morphometry is associated witha high prevalence of vertebral fractures in Duchenne Muscular Dystrophy: results from ScOT-DMD study
Shuko Joseph, Sheila Shepherd, Marina Di Marco, Jennifer Dunne, Martin McMillan, Iain Horrocks, S. Faisal Ahmed, Sze Choong Wong
Systematic screening using DXA Lateral Vertebral Morphometry is associated witha high prevalence of vertebral fractures in Duchenne Muscular Dystrophy: results from ScOT-DMD study
Shuko Joseph, Sheila Shepherd, Marina Di Marco, Jennifer Dunne, Martin McMillan, Iain Horrocks, S. Faisal Ahmed, Sze Choong Wong
P1-P032
Bone mineral density and glycemic control in children and adolescents with type 1 diabetes mellitus
Gitte Fuusager, Henrik Thybo Christesen, Nikolaj Milandt, Anders Jørgen Schou
Bone mineral density and glycemic control in children and adolescents with type 1 diabetes mellitus
Gitte Fuusager, Henrik Thybo Christesen, Nikolaj Milandt, Anders Jørgen Schou
P1-P033
Comparison of manual and automated bone age assessment in 1285 children and adolescents aged 5 to 16 years
Klara Maratova, Daniela Zemkova, Jan Lebl, Ondrej Soucek, Stepanka Pruhova, Stanislava Kolouskova, Marta Snajderova, Hana Krasnicanova, Zdenek Sumnik
Comparison of manual and automated bone age assessment in 1285 children and adolescents aged 5 to 16 years
Klara Maratova, Daniela Zemkova, Jan Lebl, Ondrej Soucek, Stepanka Pruhova, Stanislava Kolouskova, Marta Snajderova, Hana Krasnicanova, Zdenek Sumnik
P1-P034
Is Plasma C-Type Natriuretic Peptide level available for typing and diagnosis of Skeletal Dysplasia cases?
Sirmen Kizilcan Cetin, Damla Goksen, Samim Ozen, Hudaver Alper, Esra Isık, Huseyin Onay, Sukran Darcan
Is Plasma C-Type Natriuretic Peptide level available for typing and diagnosis of Skeletal Dysplasia cases?
Sirmen Kizilcan Cetin, Damla Goksen, Samim Ozen, Hudaver Alper, Esra Isık, Huseyin Onay, Sukran Darcan
P1-P035
Long-term outcomes of Osteogenesis Imperfecta in the Bisphosphonate era
Andrew Feehan, Margaret Zacharin, Angelina Lim, Peter Simm
Long-term outcomes of Osteogenesis Imperfecta in the Bisphosphonate era
Andrew Feehan, Margaret Zacharin, Angelina Lim, Peter Simm
P1-P036
Novel LRP5 loss-of-function mutation causes Osteoporosis-pseudoglioma syndrome
Debora Braslavsky, Paula Scaglia, Nora Sanguineti, Hamilton Cassinelli, Olivia Ruiz Schenstrom, Romina Armando, Claudia Arberas, Miriam Aza-Carmona, Julian Nevado-Blanco, Pablo Daniel Lapunzina-Badía, Karen E. Heath, Rodolfo Rey, Ignacio Bergadá
Novel LRP5 loss-of-function mutation causes Osteoporosis-pseudoglioma syndrome
Debora Braslavsky, Paula Scaglia, Nora Sanguineti, Hamilton Cassinelli, Olivia Ruiz Schenstrom, Romina Armando, Claudia Arberas, Miriam Aza-Carmona, Julian Nevado-Blanco, Pablo Daniel Lapunzina-Badía, Karen E. Heath, Rodolfo Rey, Ignacio Bergadá
P1-P037
Hypercalcaemia after treatment with Denosumab in children: Bisphosphonates as an option for therapy and/or prevention?
Carmen Sydlik, Claudia Weissenbacher, Julia Roeb, Hans Roland Dürr, Susanne Bechtold-Dalla Pozza, Heinrich Schmidt
Hypercalcaemia after treatment with Denosumab in children: Bisphosphonates as an option for therapy and/or prevention?
Carmen Sydlik, Claudia Weissenbacher, Julia Roeb, Hans Roland Dürr, Susanne Bechtold-Dalla Pozza, Heinrich Schmidt
P1-P038
Disease burden and systemic manifestations of HPP in children enrolled in the Global HPP Registry
Wolfgang Högler, Craig Langman, Hugo Gomes Da Silva, Shona Fang, Agnès Linglart, Keiichi Ozono, Anna Petryk, Cheryl Rockman-Greenberg, Lothar Seefried, Priya Kishnani
Disease burden and systemic manifestations of HPP in children enrolled in the Global HPP Registry
Wolfgang Högler, Craig Langman, Hugo Gomes Da Silva, Shona Fang, Agnès Linglart, Keiichi Ozono, Anna Petryk, Cheryl Rockman-Greenberg, Lothar Seefried, Priya Kishnani
P1-P039
3-epi-25 serum 25-hydroxyvitamin D3 concentrations in Chilean children between 5 and 8 years
MONICA ARANCIBIA, CRISTIAN SEILTGENS, HELENA POGGI, FIDEL ALLENDE, SANDRA SOLARI, SOLEDAD PEREDO, CLAUDIA TRINCADO, HERNAN GARCIA, ROSARIO MOORE, IVONNE DÀPREMONT, DANIELA ANDRADE, SOFIA SIFAQUI, JT OSSA, CARMEN CAMPINO, CRISTIAN CARVAJAL, CARLOS FARDELLA, RENE BAUDRAND, XIMENA SANCHEZ, ALEJANDRO MARTINEZ-AGUAYO
3-epi-25 serum 25-hydroxyvitamin D3 concentrations in Chilean children between 5 and 8 years
MONICA ARANCIBIA, CRISTIAN SEILTGENS, HELENA POGGI, FIDEL ALLENDE, SANDRA SOLARI, SOLEDAD PEREDO, CLAUDIA TRINCADO, HERNAN GARCIA, ROSARIO MOORE, IVONNE DÀPREMONT, DANIELA ANDRADE, SOFIA SIFAQUI, JT OSSA, CARMEN CAMPINO, CRISTIAN CARVAJAL, CARLOS FARDELLA, RENE BAUDRAND, XIMENA SANCHEZ, ALEJANDRO MARTINEZ-AGUAYO
P2-P036
Length estimation based on clinical and anthropometric measures in newborns.
Martha Beauregard-Paz, America L Miranda-Lora, Ana M Cruz-Hernandez, Rodolfo Rivas-Rivas, Miguel Klünder-Klünder
Length estimation based on clinical and anthropometric measures in newborns.
Martha Beauregard-Paz, America L Miranda-Lora, Ana M Cruz-Hernandez, Rodolfo Rivas-Rivas, Miguel Klünder-Klünder
P2-P037
Vitamin D deficient (nutritional) Rickets presenting in infancy
Dilusha Prematilake, Raihana Hashim, Udeni Kollurage, Navoda Atapattu
Vitamin D deficient (nutritional) Rickets presenting in infancy
Dilusha Prematilake, Raihana Hashim, Udeni Kollurage, Navoda Atapattu
P2-P038
The Effect Of Vitamin D Receptor Polymorphism On Bone Mineral Density in Egyptian Patients With Beta Thalassemia Major
.Hadeer Aly Abbassy, Reham Abdel Haleem Abo Elwafa, Omneya Magdy Omar, Aliaa Emadeldin Nassar
The Effect Of Vitamin D Receptor Polymorphism On Bone Mineral Density in Egyptian Patients With Beta Thalassemia Major
.Hadeer Aly Abbassy, Reham Abdel Haleem Abo Elwafa, Omneya Magdy Omar, Aliaa Emadeldin Nassar
P2-P039
Vitamin D in adolescents: a comprehensive review of guidelines and recommendations
Magdalini Patseadou, Dagmar Haller
Vitamin D in adolescents: a comprehensive review of guidelines and recommendations
Magdalini Patseadou, Dagmar Haller
P2-P040
X-Linked Hypophosphatemia Registry – an international prospective patient registry
Raja Padidela, Ola Nilsson, Agnès Linglart, Outi Mäkitie, Signe Beck-Nielsen, Gema Ariceta, Dirk Schnabel, Maria Luisa Brandi, Annemieke Boot, Ravi Jandhyala, Gerd Moeller, Elena Levtchenko, Zulf Mughal
X-Linked Hypophosphatemia Registry – an international prospective patient registry
Raja Padidela, Ola Nilsson, Agnès Linglart, Outi Mäkitie, Signe Beck-Nielsen, Gema Ariceta, Dirk Schnabel, Maria Luisa Brandi, Annemieke Boot, Ravi Jandhyala, Gerd Moeller, Elena Levtchenko, Zulf Mughal
P2-P041
Clinical and biological parameters associated to the severity of X-linked Hypophosphatemia in children
A Salcion-Picaud, A Rothenbuhler, A Etcheto, A Molto, K Briot, A Linglart
Clinical and biological parameters associated to the severity of X-linked Hypophosphatemia in children
A Salcion-Picaud, A Rothenbuhler, A Etcheto, A Molto, K Briot, A Linglart
P2-P042
High Fibroblast Growth Factor (FGF) 23: an unusual cause of severe Osteoporosis in a patient with chronic liver disease
Nicholas Beng Hui Ng, Yung Seng Lee, Andrew Anjian Sng, Marion Margaret Aw, Kah Yin Loke
High Fibroblast Growth Factor (FGF) 23: an unusual cause of severe Osteoporosis in a patient with chronic liver disease
Nicholas Beng Hui Ng, Yung Seng Lee, Andrew Anjian Sng, Marion Margaret Aw, Kah Yin Loke
P2-P043
Metabolic syndrome in children with X-linked hypophosphatemic rickets (XLHR)
Anne-Sophie Lambert, Sanaa Saadeddine, Anya Rothenbuhler, Alessia Ussardi, Severine Trabado, Agnès Linglart
Metabolic syndrome in children with X-linked hypophosphatemic rickets (XLHR)
Anne-Sophie Lambert, Sanaa Saadeddine, Anya Rothenbuhler, Alessia Ussardi, Severine Trabado, Agnès Linglart
P2-P044
High incidence of Cranial Synostosis and Chiari Malformation in children with X-linked Hypophosphatemic rickets
Anya Rothenbuhler, Justine Bacchetta, Nathalie Fadel, Anne Sophie Lambert, Catherine Adamsbaum, Agnes Linglart, Federicco Di Rocco
High incidence of Cranial Synostosis and Chiari Malformation in children with X-linked Hypophosphatemic rickets
Anya Rothenbuhler, Justine Bacchetta, Nathalie Fadel, Anne Sophie Lambert, Catherine Adamsbaum, Agnes Linglart, Federicco Di Rocco
P2-P045
An unusual case of hypophosphatemia in a child affected by Di George syndrome
Mila Ann Kalapurackal, Federica Barzaghi, Marco Pitea, Gilda Cassano, Giovanna Weber
An unusual case of hypophosphatemia in a child affected by Di George syndrome
Mila Ann Kalapurackal, Federica Barzaghi, Marco Pitea, Gilda Cassano, Giovanna Weber
P2-P046
Novel SLC34A1 mutation in a girl infant with idiopathic infantile hypercalcemia
Seokjin Kang, Heung Sik Kim
Novel SLC34A1 mutation in a girl infant with idiopathic infantile hypercalcemia
Seokjin Kang, Heung Sik Kim
P2-P047
A novel variant of SLC34A1 gene in an infant with Idiopathic Infantile Hypercalcemia
Gi-Min Lee, Jung-Eun Moon, Hyeon-A Kim, Su-Jeong Lee, Cheol-Woo Ko
A novel variant of SLC34A1 gene in an infant with Idiopathic Infantile Hypercalcemia
Gi-Min Lee, Jung-Eun Moon, Hyeon-A Kim, Su-Jeong Lee, Cheol-Woo Ko
P2-P048
Infantile Arterial Calcification and subsequent Hypophosphatemia due to ENPP1 mutation – a case followed through to adulthood
Munier Nour, Mark Inman, Terra Arnason
Infantile Arterial Calcification and subsequent Hypophosphatemia due to ENPP1 mutation – a case followed through to adulthood
Munier Nour, Mark Inman, Terra Arnason
P2-P049
Pediatric quality of life inventory in children with Osteogenesis Imperfect in Dr Soetomo Hospital Surabaya
Nur Rochmah, Muhammad Faizi
Pediatric quality of life inventory in children with Osteogenesis Imperfect in Dr Soetomo Hospital Surabaya
Nur Rochmah, Muhammad Faizi
P2-P050
Osteoporosis-pseudoglioma Syndrome (OPPG): improvement of osteoporosis on biphosphonate therapy
Esin Karakilic Ozturan, Umut Altunoglu, Asli Derya Kardelen, Zehra Yavas Abali, Sahin Avci, Hulya Kayserili Karabey, Sukran Poyrazoglu, Firdevs Bas, Feyza Darendeliler
Osteoporosis-pseudoglioma Syndrome (OPPG): improvement of osteoporosis on biphosphonate therapy
Esin Karakilic Ozturan, Umut Altunoglu, Asli Derya Kardelen, Zehra Yavas Abali, Sahin Avci, Hulya Kayserili Karabey, Sukran Poyrazoglu, Firdevs Bas, Feyza Darendeliler
P2-P051
Bone marrow adiposity and IGF system in obese children and adolescents
Emiliana Darrigo, Soraya Sader, Thais Siena, Marcelo Nogueira-Barbosa, Jorge Elias Jr., Rodrigo Custódio, Ivan Ferraz, Raphael Liberatore Jr., Luiz Del Ciampo, Francisco José Albuquerque de Paula, Carlos Martinelli Jr
Bone marrow adiposity and IGF system in obese children and adolescents
Emiliana Darrigo, Soraya Sader, Thais Siena, Marcelo Nogueira-Barbosa, Jorge Elias Jr., Rodrigo Custódio, Ivan Ferraz, Raphael Liberatore Jr., Luiz Del Ciampo, Francisco José Albuquerque de Paula, Carlos Martinelli Jr
P2-P052
Evaluation of bone mineral density in a cohort of children with Growth Hormone deficiency
Valentina Cenciarelli, Patrizia Bruzzi, Barbara Predieri, Caterina Cerbone, Simona Madeo, Francesco Leo
Evaluation of bone mineral density in a cohort of children with Growth Hormone deficiency
Valentina Cenciarelli, Patrizia Bruzzi, Barbara Predieri, Caterina Cerbone, Simona Madeo, Francesco Leo
P2-P053
Follow-up on bone health in children with acute lymphoblastic leukemia (ALL)
Luciana Brenzoni, Hamilton Cassinelli, Ignacio Bergada
Follow-up on bone health in children with acute lymphoblastic leukemia (ALL)
Luciana Brenzoni, Hamilton Cassinelli, Ignacio Bergada
P2-P054
Effect of Pubertal inductionn bone mass accrual, in adolescent boys with Duchenne muscular dystrophy
margaret zacharin, Samantha Lee, Tashunka Taylor Miller, peter simm, craig munns
Effect of Pubertal inductionn bone mass accrual, in adolescent boys with Duchenne muscular dystrophy
margaret zacharin, Samantha Lee, Tashunka Taylor Miller, peter simm, craig munns
P2-P055
Oxandrolone improves the linear growth and osteoporosis in teenage bays with osteogenesis imperfecta
Shadab Salehpour, Somayeh Setavand, Reza Shiari, Vahid Reza Yassaee, Mehdi Vafadar, Saeed Tavakoli
Oxandrolone improves the linear growth and osteoporosis in teenage bays with osteogenesis imperfecta
Shadab Salehpour, Somayeh Setavand, Reza Shiari, Vahid Reza Yassaee, Mehdi Vafadar, Saeed Tavakoli
P2-P056
First reported cases of a novel variant of GNAS 1 gene
Olga fafoula, Argyro Panagiotakou, Grigorios Grivas, Eleni Fryssira, Ioanna Kosteria, Paraskevi Korovessi, Stavroula Kostaridou
First reported cases of a novel variant of GNAS 1 gene
Olga fafoula, Argyro Panagiotakou, Grigorios Grivas, Eleni Fryssira, Ioanna Kosteria, Paraskevi Korovessi, Stavroula Kostaridou
P2-P057
An unusual cause of short stature
Sare Betul Kaygusuz, Zeynep Atay, Tarik Kirkgoz, Tulay Guran, Abdullah Bereket, Serap Turan
An unusual cause of short stature
Sare Betul Kaygusuz, Zeynep Atay, Tarik Kirkgoz, Tulay Guran, Abdullah Bereket, Serap Turan
P2-P058
Validation of an automated method (BoneXpert) for the determination of bone age in paediatric endocrinology -a single centre experience
Alistair Calder, Antonia Dastamani, Helen Spoudeas, Mehul Dattani
Validation of an automated method (BoneXpert) for the determination of bone age in paediatric endocrinology -a single centre experience
Alistair Calder, Antonia Dastamani, Helen Spoudeas, Mehul Dattani
P2-P059
Arthrogryposis Multiplex Congenita Type II and Panhypopituitarism
Aysun Bideci, Esra Döğer, Aylin Kılınç Uğurlu, Emine Demet Akbaş, Orhun Çamurdan, Peyami Cinaz
Arthrogryposis Multiplex Congenita Type II and Panhypopituitarism
Aysun Bideci, Esra Döğer, Aylin Kılınç Uğurlu, Emine Demet Akbaş, Orhun Çamurdan, Peyami Cinaz
P3-P031
Growth hormone treatment of 2 patients with X-linked hypophosphatemic rickets caused by PHEX mutation: effects on linear growth
Aleksandra Rojek, Monika Obara-Moszynska, Marek Niedziela
Growth hormone treatment of 2 patients with X-linked hypophosphatemic rickets caused by PHEX mutation: effects on linear growth
Aleksandra Rojek, Monika Obara-Moszynska, Marek Niedziela
P3-P032
A novel homozygous mutation in the CASR gene in a neonate with severe primary hyperparathyroidism; a case report
ALI ALQADI, ENAAM RABOEI, ABDULLAH GHAFOURI, ALBANDARI ALGUTHAMI, RAZAN ALGHANMI
A novel homozygous mutation in the CASR gene in a neonate with severe primary hyperparathyroidism; a case report
ALI ALQADI, ENAAM RABOEI, ABDULLAH GHAFOURI, ALBANDARI ALGUTHAMI, RAZAN ALGHANMI
P3-P033
A 13 Year-Old Boy Diagnosed As Osteogenesis Imperfecta With Normal Bone Mineral Density
Tuba Tınastepe, Berna Eroğlu Filibeli, Gönül Çatlı, Bumin Nuri Dündar
A 13 Year-Old Boy Diagnosed As Osteogenesis Imperfecta With Normal Bone Mineral Density
Tuba Tınastepe, Berna Eroğlu Filibeli, Gönül Çatlı, Bumin Nuri Dündar
P3-P034
A rare cause of hypercalcemia in childhood: hypercalcemia associated with parathormon-related peptid
Gönül Çatlı, Berna Eroğlu Filibeli, Belde Kasap Demir, Fatma Mutlubaş, Bumin Nuri Dündar
A rare cause of hypercalcemia in childhood: hypercalcemia associated with parathormon-related peptid
Gönül Çatlı, Berna Eroğlu Filibeli, Belde Kasap Demir, Fatma Mutlubaş, Bumin Nuri Dündar
P3-P035
Our Treatment Experience with Nocturnal Continuous Enteral Calcium Infusion in a Case with Vitamin D Resistance Rickets Type II
Berna Eroğlu Filibeli, Özgür Kırbıyık, Bumin Nuri Dündar
Our Treatment Experience with Nocturnal Continuous Enteral Calcium Infusion in a Case with Vitamin D Resistance Rickets Type II
Berna Eroğlu Filibeli, Özgür Kırbıyık, Bumin Nuri Dündar
P3-P036
A novel COL1A2 gene mutation in a Turkish family with Osteogenesis İmperfecta
Cigdem Binay, Özcan Çiftçi
A novel COL1A2 gene mutation in a Turkish family with Osteogenesis İmperfecta
Cigdem Binay, Özcan Çiftçi
P3-P037
Hypophosphatemic Hypercalciuric Ricket: 3 brothers with Dent´s Disease
Claudia Godoy, Francisca Grob, Gilberto Gonzalez, Andrea Vogel, Pedro Zambrano
Hypophosphatemic Hypercalciuric Ricket: 3 brothers with Dent´s Disease
Claudia Godoy, Francisca Grob, Gilberto Gonzalez, Andrea Vogel, Pedro Zambrano
P3-P040
A novel p.Gly775Glu missense COL1A2 mutation causes severe osteogenesis imperfecta in a prepubertal girl
Eleni P Kotanidou, Artemis Doulgeraki, Alice Costantini, Outi Makitie, Helen Athanasopoulou, Nikolaos Laliotis, Assimina Galli-Tsinopoulou
A novel p.Gly775Glu missense COL1A2 mutation causes severe osteogenesis imperfecta in a prepubertal girl
Eleni P Kotanidou, Artemis Doulgeraki, Alice Costantini, Outi Makitie, Helen Athanasopoulou, Nikolaos Laliotis, Assimina Galli-Tsinopoulou
P3-P041
SHOX gene deletion screening by FISH in children with short stature and characteristics of patients
Erdal Kurnaz, Şenay Savaş-Erdeve, Semra Çetinkaya, Zehra Aycan
SHOX gene deletion screening by FISH in children with short stature and characteristics of patients
Erdal Kurnaz, Şenay Savaş-Erdeve, Semra Çetinkaya, Zehra Aycan
P3-P042
Pseudoachondroplasia
Esra Döğer, Aysun Bideci, Öznur Boyunağa, Aylin Kılınç Uğurlu, Emine Demet Akbaş, Orhun Çamurdan, Peyami Cinaz
Pseudoachondroplasia
Esra Döğer, Aysun Bideci, Öznur Boyunağa, Aylin Kılınç Uğurlu, Emine Demet Akbaş, Orhun Çamurdan, Peyami Cinaz
P3-P043
Low level of vitamin D in children increases the risk of bone fractures
Georges Nicolas, Fady Hoyek, Elias Assaf, Georges Abi Fares, Simon Akiki
Low level of vitamin D in children increases the risk of bone fractures
Georges Nicolas, Fady Hoyek, Elias Assaf, Georges Abi Fares, Simon Akiki
P3-P044
Clinical Evaluation of Eight Patients with Parathyroid Adenoma
gül direk, zeynep uzan tatlı, merve nur hepokur, ülkü gül şiraz, leyla akın, nihal hatipoğlu, mustafa kendirci, selim kurtoğlu
Clinical Evaluation of Eight Patients with Parathyroid Adenoma
gül direk, zeynep uzan tatlı, merve nur hepokur, ülkü gül şiraz, leyla akın, nihal hatipoğlu, mustafa kendirci, selim kurtoğlu
P3-P045
Idiopathic hypoparathyroidism in a 10 year-old girl with concomitant epilepsy, Long Q-T Syndrome (LQTS), pericarditis and pneumonia
Hanna Borysewicz-Sańczyk, Beata Sawicka, Barbara Kiryluk, Piotr Szumowski, Dr Jeremy Allgrove, Artur Bossowski
Idiopathic hypoparathyroidism in a 10 year-old girl with concomitant epilepsy, Long Q-T Syndrome (LQTS), pericarditis and pneumonia
Hanna Borysewicz-Sańczyk, Beata Sawicka, Barbara Kiryluk, Piotr Szumowski, Dr Jeremy Allgrove, Artur Bossowski
P3-P046
The level of the Vitamin D and bone mineral density in children with obesity
Hanna Mikhno, Anzhalika Solntsava, Natalia Vasilieva, Helena Dashkevich
The level of the Vitamin D and bone mineral density in children with obesity
Hanna Mikhno, Anzhalika Solntsava, Natalia Vasilieva, Helena Dashkevich
P3-P047
Evaluation of bone mineral density and bone metabolism markers in hicldren diagnosed as Celiac disease
Havva Nur Peltek Kendirci, Atakan Comba, Emre Demir
Evaluation of bone mineral density and bone metabolism markers in hicldren diagnosed as Celiac disease
Havva Nur Peltek Kendirci, Atakan Comba, Emre Demir
P3-P048
Comparison of serum 25-Hydroxy vitamin D levels among children & adolescence with attention deficit hyperactivity disorder and healthy Iranian people
Heshmat Moayeri
Comparison of serum 25-Hydroxy vitamin D levels among children & adolescence with attention deficit hyperactivity disorder and healthy Iranian people
Heshmat Moayeri
P3-P049
Evaluating the effect of zoledronic acid on treatment of primary and secondary pediatric osteoporosis at Children’s Hospital 1 in Vietnam
Loan Huynh, Huyen Tran, Trung Nguyen
Evaluating the effect of zoledronic acid on treatment of primary and secondary pediatric osteoporosis at Children’s Hospital 1 in Vietnam
Loan Huynh, Huyen Tran, Trung Nguyen
P3-P051
Clinical and genetic evaluations of three patients with vitamin D dependent rickets type 1A
Kristina Kulikova, Anna Kolodkina, Eugeny Vasiliev,, Vasily Petrov, Anatoly Tiulpakov
Clinical and genetic evaluations of three patients with vitamin D dependent rickets type 1A
Kristina Kulikova, Anna Kolodkina, Eugeny Vasiliev,, Vasily Petrov, Anatoly Tiulpakov
P3-P052
A rare case of familial hypocalcemia.
Leila Sozaeva, Eda Yanar, Anotoly Tiulpakov, Maria Kareva, Elizaveta Orlova
A rare case of familial hypocalcemia.
Leila Sozaeva, Eda Yanar, Anotoly Tiulpakov, Maria Kareva, Elizaveta Orlova
P3-P053
HDR Syndrome:a case report of hypoparathyroidism, hearing loss and renal agenesis
Mihaela Dimitrova-Mladenova, Zdravka Todorova, Elisaveta Stefanova, Antoaneta Kostova, Desislava Yordanova, Polina Miteva, Dimitar Rusinov
HDR Syndrome:a case report of hypoparathyroidism, hearing loss and renal agenesis
Mihaela Dimitrova-Mladenova, Zdravka Todorova, Elisaveta Stefanova, Antoaneta Kostova, Desislava Yordanova, Polina Miteva, Dimitar Rusinov
P3-P055
The British OsteoNEcrosis Study:a multi-centre prospective study
Nadia Amin, Beki James, Richard Feltbower, Talat Mushtaq, Sally Kinsey
The British OsteoNEcrosis Study:a multi-centre prospective study
Nadia Amin, Beki James, Richard Feltbower, Talat Mushtaq, Sally Kinsey
P3-P056
Response to pamidronate therapy and pharmacogenetics in patients with Osteogenesis Imperfecta
Nalini M Selveindran, Janet YH Hong, Nadiah Mohd Nawawi, Nor Azian Abdul Murad, Rahman Jamal, Zarina Abdul Latiff, Bilkis Banu Abd Aziz, Syed Zulkifli Syed Zakaria, Fuziah Md Zain, Rahmah Rasat
Response to pamidronate therapy and pharmacogenetics in patients with Osteogenesis Imperfecta
Nalini M Selveindran, Janet YH Hong, Nadiah Mohd Nawawi, Nor Azian Abdul Murad, Rahman Jamal, Zarina Abdul Latiff, Bilkis Banu Abd Aziz, Syed Zulkifli Syed Zakaria, Fuziah Md Zain, Rahmah Rasat
P3-P057
Results of 22 weeks of burosumab therapy in a patient with severe bone deformities due to XLH
Pablo Ruiz-Ocaña, Virginia Roldán-Cano, Ana Castellano-Mendoza, Patricia Salazar-Oliva, Alfonso Lechuga-Sancho
Results of 22 weeks of burosumab therapy in a patient with severe bone deformities due to XLH
Pablo Ruiz-Ocaña, Virginia Roldán-Cano, Ana Castellano-Mendoza, Patricia Salazar-Oliva, Alfonso Lechuga-Sancho
P3-P058
Severe neonatal hypercalcemia: a challenging case
Raihana Hashim, Dilusha Prematilake, Buddi Gunasekara, Jananie Suntharesan, Udeni Kollurage, Navoda Atapattu
Severe neonatal hypercalcemia: a challenging case
Raihana Hashim, Dilusha Prematilake, Buddi Gunasekara, Jananie Suntharesan, Udeni Kollurage, Navoda Atapattu
P3-P059
Assessment of vitamin D status in healthy pre-pubertal Egyptian children
Rasha Hamza, Nadin Toeima, Amira Hamed
Assessment of vitamin D status in healthy pre-pubertal Egyptian children
Rasha Hamza, Nadin Toeima, Amira Hamed
P3-P060
Are Caucasian children at risk of sub-optimal vitamin D levels?
Krutika Shrikhande, Nancy Liu, Sankavi Thavakumar, Yadlapalli Kumar
Are Caucasian children at risk of sub-optimal vitamin D levels?
Krutika Shrikhande, Nancy Liu, Sankavi Thavakumar, Yadlapalli Kumar
P3-P061
Incidence rate of vitamin D deficiency in 12-year old children in Japan
Satomi Koyama, Junko Naganuma, Takuo Kubota, Keiichi Ozono, Osamu Arisaka, Shigemi Yoshihara
Incidence rate of vitamin D deficiency in 12-year old children in Japan
Satomi Koyama, Junko Naganuma, Takuo Kubota, Keiichi Ozono, Osamu Arisaka, Shigemi Yoshihara
P3-P062
Idiopathic Juvenile Osteoporosis: common symptoms in an uncommon condition
SAURABH UPPAL, SENTHIL SENNIAPPAN, POONAM DHARMARAJ, DAVID HUGHES
Idiopathic Juvenile Osteoporosis: common symptoms in an uncommon condition
SAURABH UPPAL, SENTHIL SENNIAPPAN, POONAM DHARMARAJ, DAVID HUGHES
P3-P063
An Internet-Based, Direct-to-Patient, Disease Registry for Ectonucleotide Pyrophosphatase/Phosphodiesterase 1, Using Data Donation Platform
Scott Sutherland, Ruhi Ahmed
An Internet-Based, Direct-to-Patient, Disease Registry for Ectonucleotide Pyrophosphatase/Phosphodiesterase 1, Using Data Donation Platform
Scott Sutherland, Ruhi Ahmed
P3-P064
Hypercalcemia associated with increased parathyroid hormone-related protein(PTHrP) in a patient with medulloblastoma successfully treated with pamidronate
SeokJin Kang, HeungSik Kim
Hypercalcemia associated with increased parathyroid hormone-related protein(PTHrP) in a patient with medulloblastoma successfully treated with pamidronate
SeokJin Kang, HeungSik Kim
P3-P065
A novel deletion mutation in the GLUT 2 gene in a patient with Fanconi Bickel syndrome
Shahab Noorian, fatemeh Aghamahdi, Samira Saee Rad
A novel deletion mutation in the GLUT 2 gene in a patient with Fanconi Bickel syndrome
Shahab Noorian, fatemeh Aghamahdi, Samira Saee Rad
P3-P066
A case of Turner syndrome with Graves' disease and primary hyperparathyroidism
Shigeru Nagaki, Emiko Tachikawa, Takao Obara, Makiko Osawa, Satoru Nagata
A case of Turner syndrome with Graves' disease and primary hyperparathyroidism
Shigeru Nagaki, Emiko Tachikawa, Takao Obara, Makiko Osawa, Satoru Nagata
P3-P067
Neonatal hypocalcemia revealing a malignant osteopetrosis.
Valérie Porquet-Bordes, Héloïse Gohier, Sandra Lescure, Marlène Pasquet, Christiane BAUNIN, Isabelle Gennero, Maïté Tauber, Jean Pierre Salles, Thomas Edouard
Neonatal hypocalcemia revealing a malignant osteopetrosis.
Valérie Porquet-Bordes, Héloïse Gohier, Sandra Lescure, Marlène Pasquet, Christiane BAUNIN, Isabelle Gennero, Maïté Tauber, Jean Pierre Salles, Thomas Edouard
P3-P068
Frontal behavior dysfunctions revealing a dramatic progression of complex cranial base abnormalities in a severe osteogenesis imperfecta
Valérie Porquet-Bordes, Naïa Grandgeorge, Pierre Moulin, Emmanuel Cheuret, Sergio Boetto, Jérôme Sales De Gauzy, Isabelle Gennero, Maïté Tauber, Thomas Edouard, Jean Pierre Salles
Frontal behavior dysfunctions revealing a dramatic progression of complex cranial base abnormalities in a severe osteogenesis imperfecta
Valérie Porquet-Bordes, Naïa Grandgeorge, Pierre Moulin, Emmanuel Cheuret, Sergio Boetto, Jérôme Sales De Gauzy, Isabelle Gennero, Maïté Tauber, Thomas Edouard, Jean Pierre Salles
P3-P069
Ionized calcium and 25-hydroxyvitamin D3 in children with steroid-sensitive nephrotic syndrome.
Yasmine Ashraf Abdelmeguid, Omneya Magdy Omar, Ola Atef Sharaki, Mahmoud Mohi El-Din El Kersh
Ionized calcium and 25-hydroxyvitamin D3 in children with steroid-sensitive nephrotic syndrome.
Yasmine Ashraf Abdelmeguid, Omneya Magdy Omar, Ola Atef Sharaki, Mahmoud Mohi El-Din El Kersh
P3-P070
Hypercalcemia due to six newly identified inactivating mutations in the CaSR gene
Yılmaz Kor
Hypercalcemia due to six newly identified inactivating mutations in the CaSR gene
Yılmaz Kor
RFC10.6
Effect of the current treatment of X-Linked Hypophosphatemia during growth on the development of osteoarticular lesions in the Hyp mouse model
Axelle Cauliez, Carole-Anne Faraji-Bellée, Benjamin Salmon, Olivier Fogel, Aurélie Benoit, Thorsten Schinke, Corinne Miceli, Karine Briot, Agnès Linglart, Catherine Chaussain, Claire Bardet
Effect of the current treatment of X-Linked Hypophosphatemia during growth on the development of osteoarticular lesions in the Hyp mouse model
Axelle Cauliez, Carole-Anne Faraji-Bellée, Benjamin Salmon, Olivier Fogel, Aurélie Benoit, Thorsten Schinke, Corinne Miceli, Karine Briot, Agnès Linglart, Catherine Chaussain, Claire Bardet
RFC11.1
Diagnosis and management of Pseudohypoparathyroidism and related disorders: first international consensus statement
Giovanna Mantovani, Murat Bastepe, David Monk, Luisa de Sanctis, Susanne Thiele, Alessia Usardi, Faisal Ahmed, Roberto Bufo, Timothée Choplin, Gianpaolo DeFillipo, Guillemette Devernois, Thomas Eggermann, Francesca M. Elli, Kathleen Freson, Aurora Garcia Ramirez, Emily Germain-Lee, Lionel Groussin, Neveen Hamdy, Patrick Hanna, Olaf Hiort, Harald Jüppner, Peter Kamenický, Nina Knight, Marie-Laure Kottler, Elvire Le Norcy, Beatriz Lecumberri, Michael A. Levine, Outi Mäkiti, Regina Martin, Gabriel Ángel Martos-Moreno, Masanori Minagawa, Philip Muray, Arrate Pereda, Roberto Pignolo, Lars Rejnmark, Rebecca Rodado, Anya Rothenbuhler, Vrinda Saraff, Ashley Shoemaker, Eileen M. Shore, Caroline Silve, Serap Turan, Philip Woods, M. Carola Zillikens, Guiomar Perez de Nanclares, Agnès Linglart
Diagnosis and management of Pseudohypoparathyroidism and related disorders: first international consensus statement
Giovanna Mantovani, Murat Bastepe, David Monk, Luisa de Sanctis, Susanne Thiele, Alessia Usardi, Faisal Ahmed, Roberto Bufo, Timothée Choplin, Gianpaolo DeFillipo, Guillemette Devernois, Thomas Eggermann, Francesca M. Elli, Kathleen Freson, Aurora Garcia Ramirez, Emily Germain-Lee, Lionel Groussin, Neveen Hamdy, Patrick Hanna, Olaf Hiort, Harald Jüppner, Peter Kamenický, Nina Knight, Marie-Laure Kottler, Elvire Le Norcy, Beatriz Lecumberri, Michael A. Levine, Outi Mäkiti, Regina Martin, Gabriel Ángel Martos-Moreno, Masanori Minagawa, Philip Muray, Arrate Pereda, Roberto Pignolo, Lars Rejnmark, Rebecca Rodado, Anya Rothenbuhler, Vrinda Saraff, Ashley Shoemaker, Eileen M. Shore, Caroline Silve, Serap Turan, Philip Woods, M. Carola Zillikens, Guiomar Perez de Nanclares, Agnès Linglart
RFC11.2
Nationwide Hypophosphatemic Rickets Study
Zeynep SIKLAR, Serap Turan, Abdullah Bereket, Ayhan Abacı, Firdevs Baş, Korcan Demir, Tülay Guran, Azad Akberzade, Ece Böber, Mehmet Nuri Özbek, Cengiz Kara, Şükran Poyrazoğlu, Murat Aydın, Aslı kardelen, Ömer tarım, Erdal Eren, Nihal Hatipoğlu, Muammer Büyükinan, Nesibe Akyürek, Semra Çetinkaya, Elvan Bayramoğlu, Beray Selver Eklioğlu, Ahmet Ucakturk, Saygın Abalı, Damla Gökşen, Yılmaz Kor, Edip Ünal, Ihsan Esen, Ruken Yıldırım, Onur Akın, Atilla Çay, Emine Dilek, Birgül Kırel, Ahmet Anık, Gönül Çatlı, Merih Berberoğlu
Nationwide Hypophosphatemic Rickets Study
Zeynep SIKLAR, Serap Turan, Abdullah Bereket, Ayhan Abacı, Firdevs Baş, Korcan Demir, Tülay Guran, Azad Akberzade, Ece Böber, Mehmet Nuri Özbek, Cengiz Kara, Şükran Poyrazoğlu, Murat Aydın, Aslı kardelen, Ömer tarım, Erdal Eren, Nihal Hatipoğlu, Muammer Büyükinan, Nesibe Akyürek, Semra Çetinkaya, Elvan Bayramoğlu, Beray Selver Eklioğlu, Ahmet Ucakturk, Saygın Abalı, Damla Gökşen, Yılmaz Kor, Edip Ünal, Ihsan Esen, Ruken Yıldırım, Onur Akın, Atilla Çay, Emine Dilek, Birgül Kırel, Ahmet Anık, Gönül Çatlı, Merih Berberoğlu
RFC11.3
Increased levels of bone formation and resorption markers in patients with hypophosphatemic rickets
Stinus Hansen, Vikram Vinod Shanbhogue, Niklas Rye Jorgensen, Signe Sparre Beck-Nielsen
Increased levels of bone formation and resorption markers in patients with hypophosphatemic rickets
Stinus Hansen, Vikram Vinod Shanbhogue, Niklas Rye Jorgensen, Signe Sparre Beck-Nielsen
RFC11.4
A new form of Anhidrotic Ectodermal Dysplasia with Immunodeficiency caused by abolished Store-Operated Ca2+ Entry
Mario Cuk, Jayson Lian, Sascha Kahlfuss, Lina Kozhaya, Martin Vaeth, Frederic Rieux-Laucat, Capucine Picard, Melina J. Benson, Antonia Jakovcevic, Karmen Bilic, Iva Martinac, Peter Stathopulos, Imre Kacskovics, Thomas Vraetz, Carsten Speckmann, Stephan Ehl, Thomas Issekutz, Derya Unutmaz, Stefan Feske
A new form of Anhidrotic Ectodermal Dysplasia with Immunodeficiency caused by abolished Store-Operated Ca2+ Entry
Mario Cuk, Jayson Lian, Sascha Kahlfuss, Lina Kozhaya, Martin Vaeth, Frederic Rieux-Laucat, Capucine Picard, Melina J. Benson, Antonia Jakovcevic, Karmen Bilic, Iva Martinac, Peter Stathopulos, Imre Kacskovics, Thomas Vraetz, Carsten Speckmann, Stephan Ehl, Thomas Issekutz, Derya Unutmaz, Stefan Feske
RFC11.5
The determinants of skeletal fragility in children with Type 1 Diabetes Mellitus
Suet Ching Chen, Sheila Shepherd, Martin McMillan, Jane McNeilly, Christie McComb, John Foster, Kenneth J Robertson, Sze Choong Wong, S Faisal Ahmed
The determinants of skeletal fragility in children with Type 1 Diabetes Mellitus
Suet Ching Chen, Sheila Shepherd, Martin McMillan, Jane McNeilly, Christie McComb, John Foster, Kenneth J Robertson, Sze Choong Wong, S Faisal Ahmed
RFC11.6
Reference Values of Automated Bone Age and Bone Health Index for Mexican children and adolescents.
América Liliana Miranda Lora, Montserrat Espinosa Espíndola, Desireé López González, Mariana Sánchez-Curiel Loyo, Pilar Dies Suárez, Miguel Klünder Klünder
Reference Values of Automated Bone Age and Bone Health Index for Mexican children and adolescents.
América Liliana Miranda Lora, Montserrat Espinosa Espíndola, Desireé López González, Mariana Sánchez-Curiel Loyo, Pilar Dies Suárez, Miguel Klünder Klünder
RFC2.1
High-resolution MRI imaging of bone-muscle-fat in glucocorticoid treated boys with Duchenne Muscular Dystrophy: results from the ScOT-DMD study
Shuko Joseph, Jennifer Dunne, Huda Elsharkasi, John Foster, Iain Horrocks, Marina Di Marco, Christine McComb, S.Faisal Ahmed, Sze Choong Wong
High-resolution MRI imaging of bone-muscle-fat in glucocorticoid treated boys with Duchenne Muscular Dystrophy: results from the ScOT-DMD study
Shuko Joseph, Jennifer Dunne, Huda Elsharkasi, John Foster, Iain Horrocks, Marina Di Marco, Christine McComb, S.Faisal Ahmed, Sze Choong Wong
RFC2.2
S-25OHD is associated with hand grip strength and myopathy at five years in girls: an Odense Child Cohort Study
Rada Faris Al-Jwadi, Eva Jespersen, Christine Dalgård, Niels Bilenberg, Henrik Thybo Christesen
S-25OHD is associated with hand grip strength and myopathy at five years in girls: an Odense Child Cohort Study
Rada Faris Al-Jwadi, Eva Jespersen, Christine Dalgård, Niels Bilenberg, Henrik Thybo Christesen
RFC2.3
Measured free 25-hydroxyvitamin D in healthy children and relationship to total 25-hydroxyvitamin D, calculated free 25-hydroxyvitamin D and vitamin D binding protein
Laura Bosch i Ara, Maria Lopez-Molina, Cecilia Santillan, Marta Murillo, Aina Valls, Joan Bel
Measured free 25-hydroxyvitamin D in healthy children and relationship to total 25-hydroxyvitamin D, calculated free 25-hydroxyvitamin D and vitamin D binding protein
Laura Bosch i Ara, Maria Lopez-Molina, Cecilia Santillan, Marta Murillo, Aina Valls, Joan Bel
RFC2.4
Novel severe skeletal dysplasia with under-mineralisation associated with reduced in utero calcium transport and TRPV6 compound heterozygous variants
Philippa Bowen, Richard Caswell, Bruce Castle, C Ross Welch, Tom Hilliard, Sarah Smithson, Sian Ellard, Christine Burren
Novel severe skeletal dysplasia with under-mineralisation associated with reduced in utero calcium transport and TRPV6 compound heterozygous variants
Philippa Bowen, Richard Caswell, Bruce Castle, C Ross Welch, Tom Hilliard, Sarah Smithson, Sian Ellard, Christine Burren
RFC2.5
Identification of characteristic neurological complications in infants with Achondroplasia by routine MRI screening
Harry Dougherty, Meera Shaunak, Melita Irving, Dominic Thompson, Moira S Cheung
Identification of characteristic neurological complications in infants with Achondroplasia by routine MRI screening
Harry Dougherty, Meera Shaunak, Melita Irving, Dominic Thompson, Moira S Cheung
RFC2.6
The novel R211Q POP1 homozygous mutation causes severe short stature but uniquely only subtle skeletal dysplasia
Maha Abdulhadi-Atwan, Tehila Klopshtock, Muna Sharaf, Ariella Weinberg-Shokrun, Ephrat Levy-Lahad, David Zangen
The novel R211Q POP1 homozygous mutation causes severe short stature but uniquely only subtle skeletal dysplasia
Maha Abdulhadi-Atwan, Tehila Klopshtock, Muna Sharaf, Ariella Weinberg-Shokrun, Ephrat Levy-Lahad, David Zangen
FC10.2
Efficacy and safety of once-weekly somapacitan in childhood growth hormone deficiency: results of a randomised open-label, controlled phase 2 trial
Lars Sävendal, Michael Rasmussen, Reiko Horikawa, Vaman Khadilkar, Tadej Battelino, Paul Saenger
Efficacy and safety of once-weekly somapacitan in childhood growth hormone deficiency: results of a randomised open-label, controlled phase 2 trial
Lars Sävendal, Michael Rasmussen, Reiko Horikawa, Vaman Khadilkar, Tadej Battelino, Paul Saenger
FC4.1
Monogenic and digenic gene mutations are present in children with idiopathic short stature (ISS).
Nora María Sanguineti, Laura Ramírez, Ana Claudia Keselman, Paula Alejandra Scaglia, María Gabriela Ropelato, María Gabriela Ballerini, Liliana Karabatas, Sabina Domené, Lucía Martucci, Débora Braslavsky, Estefania Landi, Hamilton Cassinelli, Bárbara Casali, Graciela Del Rey, Patricia Pennisi, Héctor Jasper, Martín Vázquez, Rodolfo Rey, Horacio Domené, Mariana Gutiérrez, Ignacio Bergadá
Monogenic and digenic gene mutations are present in children with idiopathic short stature (ISS).
Nora María Sanguineti, Laura Ramírez, Ana Claudia Keselman, Paula Alejandra Scaglia, María Gabriela Ropelato, María Gabriela Ballerini, Liliana Karabatas, Sabina Domené, Lucía Martucci, Débora Braslavsky, Estefania Landi, Hamilton Cassinelli, Bárbara Casali, Graciela Del Rey, Patricia Pennisi, Héctor Jasper, Martín Vázquez, Rodolfo Rey, Horacio Domené, Mariana Gutiérrez, Ignacio Bergadá
FC4.2
Effects of IGF-1R nuclear localization in glioblastoma cells
Ayelen Martin, Florencia Clément, Marcela Venara, Ignacio Bergadá, Mariana Gutierrez, Patricia Pennisi
Effects of IGF-1R nuclear localization in glioblastoma cells
Ayelen Martin, Florencia Clément, Marcela Venara, Ignacio Bergadá, Mariana Gutierrez, Patricia Pennisi
FC4.3
The reduction in longitudinal growth induced by PAPP-A2 deficiency is associated with reduced body weight, increased energy expenditure and behavior modification
Juan Suárez, Patricia Rivera, Antonio Vargas, Leticia Rubio, Fernando Rodríguez de Fonseca, Julie Chowen, Jesús Argente
The reduction in longitudinal growth induced by PAPP-A2 deficiency is associated with reduced body weight, increased energy expenditure and behavior modification
Juan Suárez, Patricia Rivera, Antonio Vargas, Leticia Rubio, Fernando Rodríguez de Fonseca, Julie Chowen, Jesús Argente
FC4.4
A cross-sectional study of IGF-I bioavailability through childhood and associations with PAPP-A2, STC2 and anthropometric data
Masanobu Fujimoto, Jane Khoury, Melissa Andrew, Vivian Hwa, Andrew Dauber
A cross-sectional study of IGF-I bioavailability through childhood and associations with PAPP-A2, STC2 and anthropometric data
Masanobu Fujimoto, Jane Khoury, Melissa Andrew, Vivian Hwa, Andrew Dauber
LB-P1
A second Growth Hormone Receptor pseudoexon mutation causing frameshift and severe postnatal growth failure
Emily Cottrell, Avinaash Maharaj, Sumana Chatterjee, Anna Grandone, Grazia Cirillo, Emanuele Miraglia del Giudice, Louise A Metherell, Helen L Storr
A second Growth Hormone Receptor pseudoexon mutation causing frameshift and severe postnatal growth failure
Emily Cottrell, Avinaash Maharaj, Sumana Chatterjee, Anna Grandone, Grazia Cirillo, Emanuele Miraglia del Giudice, Louise A Metherell, Helen L Storr
P1-P141
Autosomal Dominant Growth Hormone Deficiency due to a novel c.178G>A mutation in the GH1 gene causing instability of the mutant GH protein (p.Ala34Thr).
Bradley Miller, Jimmy Tan, Shaheena Parween, Andree Eble, Christine Ternand, Louise Gregory, Mehul Dattani, Amit Pandey
Autosomal Dominant Growth Hormone Deficiency due to a novel c.178G>A mutation in the GH1 gene causing instability of the mutant GH protein (p.Ala34Thr).
Bradley Miller, Jimmy Tan, Shaheena Parween, Andree Eble, Christine Ternand, Louise Gregory, Mehul Dattani, Amit Pandey
P1-P142
Growth hormone deficiency due to whole-gene deletion of GHRHR
Sezer Acar, Korcan Demir, Özgür Kırbıyık, Ahu Paketçi, Kadri Murat Erdoğan, Ayhan Abacı, Ece Böber
Growth hormone deficiency due to whole-gene deletion of GHRHR
Sezer Acar, Korcan Demir, Özgür Kırbıyık, Ahu Paketçi, Kadri Murat Erdoğan, Ayhan Abacı, Ece Böber
P1-P143
Severe pre- and postnatal growth retardation in a child harboring a novel homozygous IGF1 gene mutation.
Ana Claudia Keselman, Paula Alejandra Scaglia, Ayelen Martin, Romina Armando, Nora María Sanguineti, Mariana Gutiérrez, Débora Braslavsky, María Gabriela Ballerini, María Gabriela Ropelato, Hamilton Cassinelli, Bárbara Casali, Graciela Del Rey, Ángel Campos Barros, Julián Nevado Blanco, Horacio Domené, Héctor Jasper, Claudia Arberas, Rodolfo Rey, Patricia Pennisi, Pablo Lapunzina-Badía, Ignacio Bergadá
Severe pre- and postnatal growth retardation in a child harboring a novel homozygous IGF1 gene mutation.
Ana Claudia Keselman, Paula Alejandra Scaglia, Ayelen Martin, Romina Armando, Nora María Sanguineti, Mariana Gutiérrez, Débora Braslavsky, María Gabriela Ballerini, María Gabriela Ropelato, Hamilton Cassinelli, Bárbara Casali, Graciela Del Rey, Ángel Campos Barros, Julián Nevado Blanco, Horacio Domené, Héctor Jasper, Claudia Arberas, Rodolfo Rey, Patricia Pennisi, Pablo Lapunzina-Badía, Ignacio Bergadá
P1-P144
A new p.(Ile66Serfs*93) IGF2 variant is associated with SRS-like phenotype
Denise Rockstroh, Heike Pfäffle, Diana Le Duc, Franziska Rößler, Franziska Schlensog-Schuster, John T. Heiker, Jürgen Kratzsch, Wieland Kiess, Johannes Lemke, Rami Abou Jamra, Roland Pfäffle
A new p.(Ile66Serfs*93) IGF2 variant is associated with SRS-like phenotype
Denise Rockstroh, Heike Pfäffle, Diana Le Duc, Franziska Rößler, Franziska Schlensog-Schuster, John T. Heiker, Jürgen Kratzsch, Wieland Kiess, Johannes Lemke, Rami Abou Jamra, Roland Pfäffle
P1-P145
Response to growth hormone in patients with isolated familial growth hormone deficiency due to RNPC3 mutations
Lourdes Travieso-Suárez, Gabriel Martos-Moreno, Jesús Pozo, María Muñoz-Calvo, Julie Chowen, Mikko Frilander, Luis Pérez-Jurado, Federico Hawkins, Jesús Argente
Response to growth hormone in patients with isolated familial growth hormone deficiency due to RNPC3 mutations
Lourdes Travieso-Suárez, Gabriel Martos-Moreno, Jesús Pozo, María Muñoz-Calvo, Julie Chowen, Mikko Frilander, Luis Pérez-Jurado, Federico Hawkins, Jesús Argente
P1-P147
Serum IGFBP-2 concentration in neonates with potential diagnosis of growth hormone deficiency (GHD).
María Gabriela Ballerini, Débora Braslavsky, Ana Keselman, María Eugenia Rodriguez, Gabriela Gotta, María Gabriela Ropelato, Ignacio Bergadá
Serum IGFBP-2 concentration in neonates with potential diagnosis of growth hormone deficiency (GHD).
María Gabriela Ballerini, Débora Braslavsky, Ana Keselman, María Eugenia Rodriguez, Gabriela Gotta, María Gabriela Ropelato, Ignacio Bergadá
P1-P148
GH treatment causes an increase in Klotho concentration in children with growth hormone deficiency
Beata Wikiera, Monika Seifert, Julita Nocon-Bohusz, Anna Noczynska, Jacek Daroszewski
GH treatment causes an increase in Klotho concentration in children with growth hormone deficiency
Beata Wikiera, Monika Seifert, Julita Nocon-Bohusz, Anna Noczynska, Jacek Daroszewski
P1-P149
Assesment of SDF-1 and Ang-1 and Ang-2 in children with growth hormone deficiency before and after 1- year therapy with recombinant growth hormone
Beata Sawicka, Marcin Moniuszko, Kamil Grubczak, Paulina Singh, Urszula Radzikowska, Paula Mikłasz, Milena Dąbrowska, Hanna Borysewicz- Sańczyk, Artur Bossowski
Assesment of SDF-1 and Ang-1 and Ang-2 in children with growth hormone deficiency before and after 1- year therapy with recombinant growth hormone
Beata Sawicka, Marcin Moniuszko, Kamil Grubczak, Paulina Singh, Urszula Radzikowska, Paula Mikłasz, Milena Dąbrowska, Hanna Borysewicz- Sańczyk, Artur Bossowski
P1-P150
Total sum of growth hormone values obtained from growth hormone stimulation test may be useful in the diagnosis of prepubertal children with Idiopathic Growth Hormone Deficiency
Su-Jeong Lee, Jung-Eun Moon, Gi-Min Lee, Hyeon-A Kim, Cheol-Woo Ko
Total sum of growth hormone values obtained from growth hormone stimulation test may be useful in the diagnosis of prepubertal children with Idiopathic Growth Hormone Deficiency
Su-Jeong Lee, Jung-Eun Moon, Gi-Min Lee, Hyeon-A Kim, Cheol-Woo Ko
P1-P151
Growth of premature infants born small by gestational age
Tatyana Kovalenko, Anton Yuditskiy, Irina Petrova
Growth of premature infants born small by gestational age
Tatyana Kovalenko, Anton Yuditskiy, Irina Petrova
P1-P152
Microalbuminuria and glomerular filtration rate in SGA born young adults
Wesley Goedegebuure, Anita Hokken-Koelega
Microalbuminuria and glomerular filtration rate in SGA born young adults
Wesley Goedegebuure, Anita Hokken-Koelega
P1-P153
Testing the performance of a preexisting growth prediction model in a cohort of prepubertal patients born small for gestational age (SGA) receiving GH treatment in PATRO children
Christof Land, Roland Pfäffle, Karl Otfried Schwab, Heide Sommer, Carl Joachim Partsch
Testing the performance of a preexisting growth prediction model in a cohort of prepubertal patients born small for gestational age (SGA) receiving GH treatment in PATRO children
Christof Land, Roland Pfäffle, Karl Otfried Schwab, Heide Sommer, Carl Joachim Partsch
P1-P154
Early onset GH replacement in GH deficiency: Is neonatal hypoglycemia important for long term follow-up?
Ayfer Alikasifoglu, Sadiye Dicle Emet, Alev Ozon, Nazlı Gonc, Nurgun Kandemir
Early onset GH replacement in GH deficiency: Is neonatal hypoglycemia important for long term follow-up?
Ayfer Alikasifoglu, Sadiye Dicle Emet, Alev Ozon, Nazlı Gonc, Nurgun Kandemir
P1-P155
Prevalence of diabetes among children treated with growth hormone in Israel
Miri Lutski, Inbar Zuker, Carmit Libruder, Orit Blumenfeld, Zvi Zadik, Tamy Shohat, Zvi Laron
Prevalence of diabetes among children treated with growth hormone in Israel
Miri Lutski, Inbar Zuker, Carmit Libruder, Orit Blumenfeld, Zvi Zadik, Tamy Shohat, Zvi Laron
P1-P156
The Effect of Growth Hormone treatment in children after Hematopoietic stem cell transplantation
C.A. Hoekx, D. Bresters, S. Le Cessie, C. Scholte, W. Oostdijk, S.E. Hannema
The Effect of Growth Hormone treatment in children after Hematopoietic stem cell transplantation
C.A. Hoekx, D. Bresters, S. Le Cessie, C. Scholte, W. Oostdijk, S.E. Hannema
P1-P158
Patients and caregivers perspectives on a mobile app that tracks adherence and outcomes in children with growth disorders treated with recombinant human growth hormone (r-hGH)
Mark McNally, Frank Long, Henry Poskitt, Jorge Cancela, Ekaterina Koledova, Javier Sanchez Castro
Patients and caregivers perspectives on a mobile app that tracks adherence and outcomes in children with growth disorders treated with recombinant human growth hormone (r-hGH)
Mark McNally, Frank Long, Henry Poskitt, Jorge Cancela, Ekaterina Koledova, Javier Sanchez Castro
P2-P206
Identification of three novel GLI2 gene variants associated with Hypopituitarism
Lidia Castro-Feijóo, Paloma Cabanas, Jesús Barreiro, Paula Silva, M Luz Couce, Manuel Pombo, Lourdes Loidi
Identification of three novel GLI2 gene variants associated with Hypopituitarism
Lidia Castro-Feijóo, Paloma Cabanas, Jesús Barreiro, Paula Silva, M Luz Couce, Manuel Pombo, Lourdes Loidi
P2-P207
Clinical and preliminary molecular description of a cohort of patients with growth retardation due to severe primary IGF1 deficiency (GROWPATI study)
Athanasia Stoupa, Magali Viaud, Isabelle Flechtner, Graziella Pinto, Dinane Samara-Boustani, Caroline Thalassinos, Laura Gabriela González Briceño, Jacques Beltrand, Irène Netchine, Frédéric Brioude, Marie Legendre, Serge Amselem, Michel Polak
Clinical and preliminary molecular description of a cohort of patients with growth retardation due to severe primary IGF1 deficiency (GROWPATI study)
Athanasia Stoupa, Magali Viaud, Isabelle Flechtner, Graziella Pinto, Dinane Samara-Boustani, Caroline Thalassinos, Laura Gabriela González Briceño, Jacques Beltrand, Irène Netchine, Frédéric Brioude, Marie Legendre, Serge Amselem, Michel Polak
P2-P208
A novel, synonymous, heterozygous, splicing variant affecting the intracellular domain of the Growth Hormone Receptor: causality for mild growth impairment and IGF-I deficiency in an affected patient?
Alexandra Efthymiadou, Anastasios Papanastasiou, Ioannis Zarkadis, Vivian Hwa, Dionysios Chrysis
A novel, synonymous, heterozygous, splicing variant affecting the intracellular domain of the Growth Hormone Receptor: causality for mild growth impairment and IGF-I deficiency in an affected patient?
Alexandra Efthymiadou, Anastasios Papanastasiou, Ioannis Zarkadis, Vivian Hwa, Dionysios Chrysis
P2-P209
A novel mutation of type Ⅰ insulin-like growth factor receptor (IGF1R) gene in a severe short stature pedigree identified by targeted Next-generation sequencing (NGS)
YU YANG, HUI HUANG, Yang Li, Liling Xie, Ka Chen, Ting Xiong, Xian Wu
A novel mutation of type Ⅰ insulin-like growth factor receptor (IGF1R) gene in a severe short stature pedigree identified by targeted Next-generation sequencing (NGS)
YU YANG, HUI HUANG, Yang Li, Liling Xie, Ka Chen, Ting Xiong, Xian Wu
P2-P210
Severe short stature, Growth Hormone (GH) Deficiency, Hypospadias, and Microcephaly: new insights into the role of chromosome 4 long arm duplication
Basma Haris, Reem Hasnah, Saras Saraswathi, Amira Saeed, Sanaa Sharari, Idris Mohammed, Khalid Hussain
Severe short stature, Growth Hormone (GH) Deficiency, Hypospadias, and Microcephaly: new insights into the role of chromosome 4 long arm duplication
Basma Haris, Reem Hasnah, Saras Saraswathi, Amira Saeed, Sanaa Sharari, Idris Mohammed, Khalid Hussain
P2-P211
Growth hormone treatment for short stature associated with TRNT1 deficiency: a case series
Yuezhen Lin
Growth hormone treatment for short stature associated with TRNT1 deficiency: a case series
Yuezhen Lin
P2-P212
Case Report: Novel case of short stature and co-occurrence of SHOX gene mutation and Fanconi Anemia
Aristotle Panayiotopoulos, Alisha Prystowsky
Case Report: Novel case of short stature and co-occurrence of SHOX gene mutation and Fanconi Anemia
Aristotle Panayiotopoulos, Alisha Prystowsky
P2-P213
Different genetic causes of short stature in a family
Alev Tulun, Roland Pfäffle, Denise Rockstroh, Rami Abou Jamra, Julia Schmidt, Gabriele Gillessen-Kaesbach, Julia Hoppmann, Olaf Hiort
Different genetic causes of short stature in a family
Alev Tulun, Roland Pfäffle, Denise Rockstroh, Rami Abou Jamra, Julia Schmidt, Gabriele Gillessen-Kaesbach, Julia Hoppmann, Olaf Hiort
P2-P214
Incidence of cranial MRI abnormalities in patients with isolated Growth Hormone deficiency: 20 years of results
Nadia Amin, Kateryna Biliaieva, Talat Mushtaq
Incidence of cranial MRI abnormalities in patients with isolated Growth Hormone deficiency: 20 years of results
Nadia Amin, Kateryna Biliaieva, Talat Mushtaq
P2-P215
Systematic prospective study of eye funduscopy before and after starting treatment with growth hormone in 290 patients
Mogas Eduard, Martin Nieves, Yeste Diego, Castaño Luis, Clemente María, Campos Ariadna, Carrascosa Antonio
Systematic prospective study of eye funduscopy before and after starting treatment with growth hormone in 290 patients
Mogas Eduard, Martin Nieves, Yeste Diego, Castaño Luis, Clemente María, Campos Ariadna, Carrascosa Antonio
P2-P216
Incidence and prevalence of growth hormone deficiency in the Russian Federation – an analysis of two registries
Maria Vorontsova
Incidence and prevalence of growth hormone deficiency in the Russian Federation – an analysis of two registries
Maria Vorontsova
P2-P217
The BSPED National Growth Hormone (GH) Audit: trends in prescribing from 2013-2016
Leena Patel, Sheila Shepherd, Nick Shaw, Vrinda Saraff
The BSPED National Growth Hormone (GH) Audit: trends in prescribing from 2013-2016
Leena Patel, Sheila Shepherd, Nick Shaw, Vrinda Saraff
P2-P218
The rationale and design of TransCon GH
Kennett Sprogøe, Michael Beckert, Eva Mortensen, David B. Karpf, Jonathan A. Leff
The rationale and design of TransCon GH
Kennett Sprogøe, Michael Beckert, Eva Mortensen, David B. Karpf, Jonathan A. Leff
P2-P219
Baseline demographics of the TransCon Growth Hormone Phase 3 heiGHt Trial
Michael Beckert, David B. Karpf, Aimee Shu, Zhengning Lin, Jonathan A. Leff
Baseline demographics of the TransCon Growth Hormone Phase 3 heiGHt Trial
Michael Beckert, David B. Karpf, Aimee Shu, Zhengning Lin, Jonathan A. Leff
P2-P220
The ZOMATRIP study: Four year combination therapy of GH and GnRHa in girls with a short predicted adult height during early puberty: adult height outcome.
Hilde Dotremont, Annick France, Claudine Heinrichs, Sylvie Tenoutasse, Cécile Brachet, Martine Cools, Kathleen De Waele, Guy Massa, Marie-Christine Lebrethon, Inge Gies, Jesse Van Besien, Christine Derycke, Jean De Schepper, Raoul Rooman
The ZOMATRIP study: Four year combination therapy of GH and GnRHa in girls with a short predicted adult height during early puberty: adult height outcome.
Hilde Dotremont, Annick France, Claudine Heinrichs, Sylvie Tenoutasse, Cécile Brachet, Martine Cools, Kathleen De Waele, Guy Massa, Marie-Christine Lebrethon, Inge Gies, Jesse Van Besien, Christine Derycke, Jean De Schepper, Raoul Rooman
P2-P221
Growth hormone treatment in children born small for gestational age (SGA)
Aleksandra Janchevska, Marina Krstevska-Konstantinova, Olivera Jordanova, Liljana Tasevska-Rmush, Velibor Tasic, Zoran Gucev
Growth hormone treatment in children born small for gestational age (SGA)
Aleksandra Janchevska, Marina Krstevska-Konstantinova, Olivera Jordanova, Liljana Tasevska-Rmush, Velibor Tasic, Zoran Gucev
P2-P222
Height perception of children with Growth Hormone Deficiency: influencing factors and links to psychosocial functioning
Chrysoula Drosatou, Elpis - Athina Vlachopapadopoulou, Monika Bullinger, Julia Quitmann, Neuza Silva, Stefanos Michalacos, Konstantinos Tsoumakas
Height perception of children with Growth Hormone Deficiency: influencing factors and links to psychosocial functioning
Chrysoula Drosatou, Elpis - Athina Vlachopapadopoulou, Monika Bullinger, Julia Quitmann, Neuza Silva, Stefanos Michalacos, Konstantinos Tsoumakas
P2-P223
Health lifestyle and obesity of adult patients with Congenital Isolated Growth Hormone Deficiency treated in childhood
Efrat Ben Nun-Yaari, Rivka Kauli, Pearl Lilos, Zvi Laron
Health lifestyle and obesity of adult patients with Congenital Isolated Growth Hormone Deficiency treated in childhood
Efrat Ben Nun-Yaari, Rivka Kauli, Pearl Lilos, Zvi Laron
P2-P224
Factors influencing Health Related Quality of Life in children/adolescents with Growth Hormone Deficiency
Chrysoula Drosatou, Elpis -Athina Vlachopapadopoulou, Julia Quitmann, Monika Bullinger, Neuza Silva, Stefanos Michalacos, Konstantinos Tsoumakas
Factors influencing Health Related Quality of Life in children/adolescents with Growth Hormone Deficiency
Chrysoula Drosatou, Elpis -Athina Vlachopapadopoulou, Julia Quitmann, Monika Bullinger, Neuza Silva, Stefanos Michalacos, Konstantinos Tsoumakas
P2-P225
Health-related quality of life and psychosocial functioning in young adults born SGA after GH/GnRHa treatment
Wesley Goedegebuure, Manouk van der Steen, Justine de With, Anita Hokken-Koelega
Health-related quality of life and psychosocial functioning in young adults born SGA after GH/GnRHa treatment
Wesley Goedegebuure, Manouk van der Steen, Justine de With, Anita Hokken-Koelega
P2-P226
Adherence to Treatment in Growth Hormone Deficient and Small for Gestational Age Patients Naïve to EasypodTM in Mexico: Final Results of the EasypodTM Connect Observational Study (ECOS)
Armando Blanco-López, Carlos Antillón-Ferreira, Eloisa Saavedra-Castillo, Margarita Barrientos-Pérez, Héctor Rivero-Escalante, Oscar Flores-Caloca, Raúl Calzada-León, Carmen Celeste Rosas-Guerra, Ekaterina Koledova, Arturo Ayala-Estrada
Adherence to Treatment in Growth Hormone Deficient and Small for Gestational Age Patients Naïve to EasypodTM in Mexico: Final Results of the EasypodTM Connect Observational Study (ECOS)
Armando Blanco-López, Carlos Antillón-Ferreira, Eloisa Saavedra-Castillo, Margarita Barrientos-Pérez, Héctor Rivero-Escalante, Oscar Flores-Caloca, Raúl Calzada-León, Carmen Celeste Rosas-Guerra, Ekaterina Koledova, Arturo Ayala-Estrada
P2-P227
Growth pattern and final height outcome in children with Septo-optic Dysplasia and isolated Hypopituitarism treated with rhGH in a single centre
Manuela Cerbone, Maria Güemes, Nicola Improda, Mehul T Dattani
Growth pattern and final height outcome in children with Septo-optic Dysplasia and isolated Hypopituitarism treated with rhGH in a single centre
Manuela Cerbone, Maria Güemes, Nicola Improda, Mehul T Dattani
P2-P228
Reliability of clonidine testing for the diagnosis of Growth Hormone Deficiency in children and adolescents
Anastasia Ibba, Chiara Guzzetti, Letizia Casula, Mariacarolina Salerno, Natascia Di Iorgi, Anna Maria Elsa Allegri, Marco Cappa, Mohamad Maghnie, Sandro Loche
Reliability of clonidine testing for the diagnosis of Growth Hormone Deficiency in children and adolescents
Anastasia Ibba, Chiara Guzzetti, Letizia Casula, Mariacarolina Salerno, Natascia Di Iorgi, Anna Maria Elsa Allegri, Marco Cappa, Mohamad Maghnie, Sandro Loche
P2-P229
Area under the curve of Growth Hormone, an additional tool in assessing stimulation test results
Yonatan Yeshayahu, Shirly Frizinsky
Area under the curve of Growth Hormone, an additional tool in assessing stimulation test results
Yonatan Yeshayahu, Shirly Frizinsky
P2-P230
Evaluation of spontaneous nocturnal GH secretion: noe versus two consecutive nights
Gunter Šimić-Schleicher
Evaluation of spontaneous nocturnal GH secretion: noe versus two consecutive nights
Gunter Šimić-Schleicher
P2-P231
Relationship between growth velocity and change of serum insulin-like growth factor-1 (IGF-1), serum IGF binding protein-3 (IGFBP-3) concentrations, and IGFBP-3 promoter polymorphism during gonadotropin-releasing hormone agonist (GnRHa) treatment
Seung Yang, Young Suk Shim, Il Tae Hwang
Relationship between growth velocity and change of serum insulin-like growth factor-1 (IGF-1), serum IGF binding protein-3 (IGFBP-3) concentrations, and IGFBP-3 promoter polymorphism during gonadotropin-releasing hormone agonist (GnRHa) treatment
Seung Yang, Young Suk Shim, Il Tae Hwang
P2-P232
The predictive role of IGF-1 on irradiation-dependent growth hormone deficiency (GHD) in childhood cancer survivors (CCS)
Alessandro Cattoni, Assunta Albanese
The predictive role of IGF-1 on irradiation-dependent growth hormone deficiency (GHD) in childhood cancer survivors (CCS)
Alessandro Cattoni, Assunta Albanese
P2-P233
Effects of zinc, magnesium and vitamin B6 (ZMA) supplementation on serum IGF-I, IGFBP-3 and testosterone concentrations in young athletes
Henrique Cerqueira, Hugo Tourinho Filho, Carlos Martinelli Jr
Effects of zinc, magnesium and vitamin B6 (ZMA) supplementation on serum IGF-I, IGFBP-3 and testosterone concentrations in young athletes
Henrique Cerqueira, Hugo Tourinho Filho, Carlos Martinelli Jr
P2-P234
High protein nutritional supplementation increases serum IGF-I concentrations in short children with low IGF-I
Elin Mattsson, Peter Bang
High protein nutritional supplementation increases serum IGF-I concentrations in short children with low IGF-I
Elin Mattsson, Peter Bang
P2-P235
Hormonal predictors of growth hormone therapy effectiveness in children with short stature – evidence from neural prediction model for final height
Maciej Hilczer, Joanna Smyczynska, Smyczynska Urszula, Renata Stawerska, Andrzej Lewinski
Hormonal predictors of growth hormone therapy effectiveness in children with short stature – evidence from neural prediction model for final height
Maciej Hilczer, Joanna Smyczynska, Smyczynska Urszula, Renata Stawerska, Andrzej Lewinski
P2-P236
Artificial neural networks for prediction final height in children with growth hormone deficiency.
Anna Gavrilova, Elena Nagaeva, Olga Rebrova, Tatiana Shiryaeva, Valentina Peterkova
Artificial neural networks for prediction final height in children with growth hormone deficiency.
Anna Gavrilova, Elena Nagaeva, Olga Rebrova, Tatiana Shiryaeva, Valentina Peterkova
P2-P237
Predictors of poor response to growth hormone therapy in children with short stature – evidence from neural prediction model for final height
Joanna Smyczynska, Urszula Smyczynska, Maciej Hilczer, Renata Stawerska, Andrzej Lewinski
Predictors of poor response to growth hormone therapy in children with short stature – evidence from neural prediction model for final height
Joanna Smyczynska, Urszula Smyczynska, Maciej Hilczer, Renata Stawerska, Andrzej Lewinski
P2-P238
Growth Hormone Therapy and its challenges in GH deficient cases in a multinational population-a sneak-peek
Deepti Chaturvedi
Growth Hormone Therapy and its challenges in GH deficient cases in a multinational population-a sneak-peek
Deepti Chaturvedi
P3-P192
Good Growth Response to Growth Hormone Therapy in Short Children with Normal Growth Hormone Secretion
Ahmed El Awwa, Ashraf Soliman
Good Growth Response to Growth Hormone Therapy in Short Children with Normal Growth Hormone Secretion
Ahmed El Awwa, Ashraf Soliman
P3-P193
Growth hormone deficiency intwo children with Williams-Beuren syndrome. The long-term response to growth hormone (GH) therapy
ASHRAF SOLIMAN, Ashraf Adel, fawzia Alyafiei
Growth hormone deficiency intwo children with Williams-Beuren syndrome. The long-term response to growth hormone (GH) therapy
ASHRAF SOLIMAN, Ashraf Adel, fawzia Alyafiei
P3-P194
Growth hormone treatment: does timing matter?
Bernardo Marques, Sónia Madeira Gomes, Joana Serra Caetano, Rita Cardoso, Isabel Dinis, Alice Mirante, Ana Laura Fitas, Catarina Diamantino, Catarina Limbert, Rosa Pina, Lurdes Lopes
Growth hormone treatment: does timing matter?
Bernardo Marques, Sónia Madeira Gomes, Joana Serra Caetano, Rita Cardoso, Isabel Dinis, Alice Mirante, Ana Laura Fitas, Catarina Diamantino, Catarina Limbert, Rosa Pina, Lurdes Lopes
P3-P195
Support for patients treated with growth hormone to reach their growth potential: addressing adherence barriers through personalised behavioural patient-support programmes
Clare Moloney, Sumaira Malik, Jorge Cancela, Ekaterina Koledova
Support for patients treated with growth hormone to reach their growth potential: addressing adherence barriers through personalised behavioural patient-support programmes
Clare Moloney, Sumaira Malik, Jorge Cancela, Ekaterina Koledova
P3-P196
Main discrepancies between predicted and observed growth responses with iGRO in children treated with GHr in Spain
Cristina Mora Palma, Nerea Itza Martín, Julio Guerrero Fernández, Luis Salamanca Fresno, Ana Coral Barreda Bonis, Isabel González Casado
Main discrepancies between predicted and observed growth responses with iGRO in children treated with GHr in Spain
Cristina Mora Palma, Nerea Itza Martín, Julio Guerrero Fernández, Luis Salamanca Fresno, Ana Coral Barreda Bonis, Isabel González Casado
P3-P197
Adherence and long-term outcomes of therapy in pediatric subjects in Greece using easypod™ electromechanical device for growth hormone treatment: the Phase IV multicentre Easypod™ Connect Observational Study (ECOS)
Evangelia Charmandari, Stefanos Michalakos, Dimitris Sakellariou, Ekaterina Koledova, George Chrousos
Adherence and long-term outcomes of therapy in pediatric subjects in Greece using easypod™ electromechanical device for growth hormone treatment: the Phase IV multicentre Easypod™ Connect Observational Study (ECOS)
Evangelia Charmandari, Stefanos Michalakos, Dimitris Sakellariou, Ekaterina Koledova, George Chrousos
P3-P198
Growth hormone deficiency in neurofibromatosis: report of four cases
Elisa Guidoni, Federica Lotti, Ursula Geronzi, Laura Arianna Sorrentino, Salvatore Grosso, Giovanna Municchi
Growth hormone deficiency in neurofibromatosis: report of four cases
Elisa Guidoni, Federica Lotti, Ursula Geronzi, Laura Arianna Sorrentino, Salvatore Grosso, Giovanna Municchi
P3-P199
EXTREMELY LOW BODY MASS INDEX NEGATIVELY IMPACT THE RESPONSE TO GROWTH HORMONE TREATMENT IN CHILDREN WITH GROWTH HORMONE DEFICIENCY
Irina Delia Nicolaescu, Denisa Dinca, Alice Albu
EXTREMELY LOW BODY MASS INDEX NEGATIVELY IMPACT THE RESPONSE TO GROWTH HORMONE TREATMENT IN CHILDREN WITH GROWTH HORMONE DEFICIENCY
Irina Delia Nicolaescu, Denisa Dinca, Alice Albu
P3-P200
Small for gestational age (SGA) patients with premature treatment discontinuation: their journey in French real-life settings
Jean-Pierre Salles, Régis Coutant, Bruno Leheup, Marc Nicolino, Evguenia Hacques, Béatrice Villette
Small for gestational age (SGA) patients with premature treatment discontinuation: their journey in French real-life settings
Jean-Pierre Salles, Régis Coutant, Bruno Leheup, Marc Nicolino, Evguenia Hacques, Béatrice Villette
P3-P201
Effects on near-adult height and safety of recombinant Human Growth Hormone in Growth Hormone Deficiency and Turner Syndrome patients: results from the LG Growth Study
Jin-Ho Choi, Sochung Chung, Young-Jun Rhee, Jae Hyun Kim, Hyun-Wook Chae, Jae-ho Yoo, Young Ah Lee, Il Tae Hwang
Effects on near-adult height and safety of recombinant Human Growth Hormone in Growth Hormone Deficiency and Turner Syndrome patients: results from the LG Growth Study
Jin-Ho Choi, Sochung Chung, Young-Jun Rhee, Jae Hyun Kim, Hyun-Wook Chae, Jae-ho Yoo, Young Ah Lee, Il Tae Hwang
P3-P202
Final adult height after growth hormone treatment in patients with Turner syndrome
Jungmin Ahn, Junghwan Suh, Hoseong Kim, Ahreum Kwon
Final adult height after growth hormone treatment in patients with Turner syndrome
Jungmin Ahn, Junghwan Suh, Hoseong Kim, Ahreum Kwon
P3-P203
Results of mecasermin treatment in pediatric patients evaluated for severe and partial primary deficiency of IGF-1
Karolina Stozek, Artur Bossowski
Results of mecasermin treatment in pediatric patients evaluated for severe and partial primary deficiency of IGF-1
Karolina Stozek, Artur Bossowski
P3-P204
Children born small for gestational age treated with growth hormone: evolutionary aspects
Verónica María Padín Vázquez, David Albino Gómez Costa, Aida Del Campo García, Lourdes Rey Cordo, Jose Luis Chamorro Martín, Jose Ramón Fernández Lorenzo
Children born small for gestational age treated with growth hormone: evolutionary aspects
Verónica María Padín Vázquez, David Albino Gómez Costa, Aida Del Campo García, Lourdes Rey Cordo, Jose Luis Chamorro Martín, Jose Ramón Fernández Lorenzo
P3-P205
”Small for gestational age (SGA) patients in real life French clinical practice: what is the difference between good and poor responders to GH treatment”
Marc Nicolino, Régis Coutant, Bruno Leheup, Jean-Pierre Salles, Evguenia Hacques, Béatice Villette
”Small for gestational age (SGA) patients in real life French clinical practice: what is the difference between good and poor responders to GH treatment”
Marc Nicolino, Régis Coutant, Bruno Leheup, Jean-Pierre Salles, Evguenia Hacques, Béatice Villette
P3-P206
Body Mass Index (BMI) in patients with Growth Hormone Deficiency (GHD) at diagnosis, one year and two years after treatment with Growth Hormone (GH)
Maria Claudia Schmitt-Lobe, Debora Regina Andrade Dalla Costa, Rafael Koji Yoshimatsu Ueno
Body Mass Index (BMI) in patients with Growth Hormone Deficiency (GHD) at diagnosis, one year and two years after treatment with Growth Hormone (GH)
Maria Claudia Schmitt-Lobe, Debora Regina Andrade Dalla Costa, Rafael Koji Yoshimatsu Ueno
P3-P207
Erythropoietin and Granulocyte Macrophage colony stimulating factor levels in Growth Hormone deficient children after 1 year of Growth Hormone therapy
Maria Pankratova, Maria Vorontsova, Alexander Yusipovich, Tatiana Shiryaeva, Valentina Peterkova
Erythropoietin and Granulocyte Macrophage colony stimulating factor levels in Growth Hormone deficient children after 1 year of Growth Hormone therapy
Maria Pankratova, Maria Vorontsova, Alexander Yusipovich, Tatiana Shiryaeva, Valentina Peterkova
P3-P208
Cost-effectiveness of growth hormone therapy in children in Russia
Maria Vorontsova, Elena Nagaeva, Nelli Naigovzina
Cost-effectiveness of growth hormone therapy in children in Russia
Maria Vorontsova, Elena Nagaeva, Nelli Naigovzina
P3-P209
Vitamin D status in children with isolated idiopathic Growth hormone deficiency (GHD) in North and Central Greece
Kyriaki Tsiroukidou, Maria Xatzipsalti, Iliana Mameka, Ioulia Polychroni, Anastasios Vamvakis, Maria Papagianni, Lela Stamogiannou
Vitamin D status in children with isolated idiopathic Growth hormone deficiency (GHD) in North and Central Greece
Kyriaki Tsiroukidou, Maria Xatzipsalti, Iliana Mameka, Ioulia Polychroni, Anastasios Vamvakis, Maria Papagianni, Lela Stamogiannou
P3-P210
A pilot study for comparing efficacy and safety of the CinnaTropin® to the reference recombinant human growth hormone in children with isolated growth hormone deficiency and multiple pituitary hormone deficiency
Maryam Razzaghy-Azar, Abdoreza Pourmotabbed, Ramin Heshmat, Farhang Rezaei
A pilot study for comparing efficacy and safety of the CinnaTropin® to the reference recombinant human growth hormone in children with isolated growth hormone deficiency and multiple pituitary hormone deficiency
Maryam Razzaghy-Azar, Abdoreza Pourmotabbed, Ramin Heshmat, Farhang Rezaei
P3-P211
Study of the effectiveness of growth hormone in children born small for gestational age in an area of northwestern Spain and its associated factors
Paloma Cabanas Rodríguez, Lourdes Rey Cordo, Antonio Bello Fernández, Jose Luis Chamorro Martín, Ana Prado Carro, Ruben Rego, Lidia Castro-Feijóo, Alicia Cepedano Dans, Jesús Barreiro Conde
Study of the effectiveness of growth hormone in children born small for gestational age in an area of northwestern Spain and its associated factors
Paloma Cabanas Rodríguez, Lourdes Rey Cordo, Antonio Bello Fernández, Jose Luis Chamorro Martín, Ana Prado Carro, Ruben Rego, Lidia Castro-Feijóo, Alicia Cepedano Dans, Jesús Barreiro Conde
P3-P212
Height velocity and height gain in the first year of growth hormone (GH) treatment: predictive factors of good statural response in small for gestational age (SGA) patients.
Régis Coutant, Bruno Leheup, Marc Nicolino, Jean-Pierre Salles, Evguenia Hacques, Béatrice Villette
Height velocity and height gain in the first year of growth hormone (GH) treatment: predictive factors of good statural response in small for gestational age (SGA) patients.
Régis Coutant, Bruno Leheup, Marc Nicolino, Jean-Pierre Salles, Evguenia Hacques, Béatrice Villette
P3-P213
Role of insulin like growth factors on the growth parameters in children with acquired hypothyroidism: an analysis
Sangita Yadav, Ruchi Goel, Mukta Mantan, T K Mishra
Role of insulin like growth factors on the growth parameters in children with acquired hypothyroidism: an analysis
Sangita Yadav, Ruchi Goel, Mukta Mantan, T K Mishra
P3-P214
Two siblings with short stature
SRI NAGESH.V, ANDREW DAUBER, RAVISHANKAR KANITHI, DEEP DUTTA, RAM KUMAR G
Two siblings with short stature
SRI NAGESH.V, ANDREW DAUBER, RAVISHANKAR KANITHI, DEEP DUTTA, RAM KUMAR G
P3-P215
RHGH replacement therapy and side- effects: Α retrospective study of 10 years
Stavroula Parastatidou, Dionysia Lampropoulou, Paraskevi Zosi, Soultana Georga, Elissavet Eufraimidou, Thomais Vlachou
RHGH replacement therapy and side- effects: Α retrospective study of 10 years
Stavroula Parastatidou, Dionysia Lampropoulou, Paraskevi Zosi, Soultana Georga, Elissavet Eufraimidou, Thomais Vlachou
P3-P216
Efficacy and safety of recombinant human growth hormone in treating Chinese children with idiopathic short stature
Yanqin Ying, Ling Hou, Liang Yan, Wei Wu, Xiaoping Luo
Efficacy and safety of recombinant human growth hormone in treating Chinese children with idiopathic short stature
Yanqin Ying, Ling Hou, Liang Yan, Wei Wu, Xiaoping Luo
P3-P217
Comparison the Recombinant Human Growth Hormone（rhGH） Treatment in Children with Idiopathic Short Stature（ISS） and Growth Hormone Deficiency（GHD）
Yanqin ying, Ling Hou, Yan Liang, Wei Wu, Xiaoping Luo
Comparison the Recombinant Human Growth Hormone（rhGH） Treatment in Children with Idiopathic Short Stature（ISS） and Growth Hormone Deficiency（GHD）
Yanqin ying, Ling Hou, Yan Liang, Wei Wu, Xiaoping Luo
P3-P218
Bone age maturation during the three years of growth hormone treatment in patients with idiopathic growth hormone deficiency and idiopathic short stature: Analysis of data from LG Growth Study
Young Suk Shim, Il Tae Hwang, Seung Yang, Eun Young Kim
Bone age maturation during the three years of growth hormone treatment in patients with idiopathic growth hormone deficiency and idiopathic short stature: Analysis of data from LG Growth Study
Young Suk Shim, Il Tae Hwang, Seung Yang, Eun Young Kim
P3-P398
Recombinant growth hormone therapy in prepubertal children with idiopathic short stature in Korea : a phase III randomized trial
Minji Im, J. Kim, B.-K. Suh, C. W. Ko, K.-H. Lee, C. H. Shin, J. S. Hwang, H. S. Kim, W. Y. Chung, C. J. Kim, H.-S. Han, N. Y. Kwon, S. Y. Cho, H.-W. Yoo, D.-K. Jin
Recombinant growth hormone therapy in prepubertal children with idiopathic short stature in Korea : a phase III randomized trial
Minji Im, J. Kim, B.-K. Suh, C. W. Ko, K.-H. Lee, C. H. Shin, J. S. Hwang, H. S. Kim, W. Y. Chung, C. J. Kim, H.-S. Han, N. Y. Kwon, S. Y. Cho, H.-W. Yoo, D.-K. Jin
RFC4.1
Metabolomic changes in patients with PAPP-A2 deficiency in response to rhIGF1 treatment
Annalaura Mastrangelo, Gabriel Martos-Moreno, Javier Rupérez, Julie Chowen, Coral Barbas, Jesús Argente
Metabolomic changes in patients with PAPP-A2 deficiency in response to rhIGF1 treatment
Annalaura Mastrangelo, Gabriel Martos-Moreno, Javier Rupérez, Julie Chowen, Coral Barbas, Jesús Argente
RFC4.2
Data mining and computational analysis of human growth hormone gene (GH1) sequence in normal population to identify potential variants with disease-causing effects
Sonia Verma, Amit V Pandey
Data mining and computational analysis of human growth hormone gene (GH1) sequence in normal population to identify potential variants with disease-causing effects
Sonia Verma, Amit V Pandey
RFC4.3
A deletion encompassing Exon 2 of the ALS gene: analysis of a patient with ALS deficiency and his family
Helena Poggi, Monica Arancibia, Felipe Benavides, Carlos Lagos, Andrea Vecchiola, Gonzalo Dominguez-Menendez, Alejandro Martinez-Aguayo
A deletion encompassing Exon 2 of the ALS gene: analysis of a patient with ALS deficiency and his family
Helena Poggi, Monica Arancibia, Felipe Benavides, Carlos Lagos, Andrea Vecchiola, Gonzalo Dominguez-Menendez, Alejandro Martinez-Aguayo
RFC4.4
A longitudinal study on miRNAs circulating levels in a cohort of SGA and AGA subjects, evaluated during childhood and young adulthood
elena inzaghi, Anna Kistner, annalisa deodati, Daniela Germani, Lena Legnevall, Mireille Vanpee, Katarina Berinder, stefano cianfarani
A longitudinal study on miRNAs circulating levels in a cohort of SGA and AGA subjects, evaluated during childhood and young adulthood
elena inzaghi, Anna Kistner, annalisa deodati, Daniela Germani, Lena Legnevall, Mireille Vanpee, Katarina Berinder, stefano cianfarani
RFC4.5
12-Month effects of once-weekly and twice-monthly administration of hybrid Fc-fused human growth hormone, GX-H9, treatment in pediatric with GHD deficiency
Oleg Malievskiy, Aryaev Mykola, Zelinska Nataliya, Elena V. Bolshova, Ganna Senatorova, György Oroszlán, Julia Skorodok, Valentina Peterkova, Chorna Nataliya, Tamila Sorokman, Seung Yang, Ji Eun Lee, Agota Muzsnai, Jin Soon Hwang, Sang Yoon Lee, Yun Jung Choi, Hyi-Jeong Ji, Jungwon Woo, Young-Chul Sung
12-Month effects of once-weekly and twice-monthly administration of hybrid Fc-fused human growth hormone, GX-H9, treatment in pediatric with GHD deficiency
Oleg Malievskiy, Aryaev Mykola, Zelinska Nataliya, Elena V. Bolshova, Ganna Senatorova, György Oroszlán, Julia Skorodok, Valentina Peterkova, Chorna Nataliya, Tamila Sorokman, Seung Yang, Ji Eun Lee, Agota Muzsnai, Jin Soon Hwang, Sang Yoon Lee, Yun Jung Choi, Hyi-Jeong Ji, Jungwon Woo, Young-Chul Sung
RFC4.6
Effect of 2 years of Growth Hormone treatment on glucose tolerance in adults with Prader-Willi syndrome
Layla Damen, Stephany Donze, Renske Kuppens, Nienke Bakker, Anita Hokken-Koelega
Effect of 2 years of Growth Hormone treatment on glucose tolerance in adults with Prader-Willi syndrome
Layla Damen, Stephany Donze, Renske Kuppens, Nienke Bakker, Anita Hokken-Koelega
FC10.3
Identification of the MAPK/ERK pathway as a novel therapeutic target in adamantinomatous craniopharyngioma
Romain Guiho, John R. Apps, Ying Hong, Darren Hargrave, Paul Brogan, Thomas S. Jacques, Juan Pedro Martinez-Barbera
Identification of the MAPK/ERK pathway as a novel therapeutic target in adamantinomatous craniopharyngioma
Romain Guiho, John R. Apps, Ying Hong, Darren Hargrave, Paul Brogan, Thomas S. Jacques, Juan Pedro Martinez-Barbera
FC10.4
Hypothalamus sparing surgery improves the outcome of patients with severe initial hypothalamic involvement of childhood craniopharyngioma: Results of the Prospective Multinational Trial KRANIOPHARYNGEOM 2007
Agnieszka Bogusz, Svenja Boekhoff, Monika Warmuth-Metz, Gabriele Calaminus, Maria Eveslage, Hermann L. Müller
Hypothalamus sparing surgery improves the outcome of patients with severe initial hypothalamic involvement of childhood craniopharyngioma: Results of the Prospective Multinational Trial KRANIOPHARYNGEOM 2007
Agnieszka Bogusz, Svenja Boekhoff, Monika Warmuth-Metz, Gabriele Calaminus, Maria Eveslage, Hermann L. Müller
FC13.1
Molecular screening of genes associated with central precocious puberty
Pavlos Fanis, Vassos Neocleous, Meropi Toumba, Barbara Gorka, Charilaos Stylianou, Assimina Galli-Tsinopoulou, Stella Nicolaou, Andreas Kyriakou, Meropi Dimitriadou, Athanasios Christoforidis, Nicos Skordis, Leonidas A. Phylactou
Molecular screening of genes associated with central precocious puberty
Pavlos Fanis, Vassos Neocleous, Meropi Toumba, Barbara Gorka, Charilaos Stylianou, Assimina Galli-Tsinopoulou, Stella Nicolaou, Andreas Kyriakou, Meropi Dimitriadou, Athanasios Christoforidis, Nicos Skordis, Leonidas A. Phylactou
FC13.2
Ablation of AgRP Neurons Decreases Survival In Activity-Based Anorexia Model
Maria Consolata Miletta, Tamas L. Horvath
Ablation of AgRP Neurons Decreases Survival In Activity-Based Anorexia Model
Maria Consolata Miletta, Tamas L. Horvath
FC13.3
Role of GnRH neuronal migration and development in Self-Limited Delayed Puberty
Sasha Howard, Roberto Oleari, Alessandra Mancini, Ariel Poliandri, Tansit Saengkaew, Leo Guasti, Anna Cariboni, Leo Dunkel
Role of GnRH neuronal migration and development in Self-Limited Delayed Puberty
Sasha Howard, Roberto Oleari, Alessandra Mancini, Ariel Poliandri, Tansit Saengkaew, Leo Guasti, Anna Cariboni, Leo Dunkel
FC13.4
The Kallman syndrome gene product is specifically expressed in ACTH-expressing cells and dysplays sexual dimorphism expression in human fetal pituitary
Fabien Guimiot, Adeline Bonnard, Nadia Soussi-Yaniscostas, Carol Schnoll, Nicolas de Roux
The Kallman syndrome gene product is specifically expressed in ACTH-expressing cells and dysplays sexual dimorphism expression in human fetal pituitary
Fabien Guimiot, Adeline Bonnard, Nadia Soussi-Yaniscostas, Carol Schnoll, Nicolas de Roux
FC13.5
Study of the serum kisspeptin level in healthy and hypogonadotropic boys
Irina Nikitina, Yulia Khoduleva, Irena Nagornaya, Elena Vasileva
Study of the serum kisspeptin level in healthy and hypogonadotropic boys
Irina Nikitina, Yulia Khoduleva, Irena Nagornaya, Elena Vasileva
FC9.1
Novel variants in the POU1F1 beta isoform are associated with isolated growth hormone deficiency and combined pituitary hormone deficiency
Julia Hoppmann, Denise Rockstroh-Lippold, Peter Gergics, Marilena Nakaguma, Luciani Renata Silveira Carvalho, Heike Pfaeffle, Rami Abou Jamra, Alexander Jorge, Michael H. Guo, Andrew Dauber, Eberhard Keller, Sally A. Camper, Ivo JP Arnhold, Roland Pfaeffle
Novel variants in the POU1F1 beta isoform are associated with isolated growth hormone deficiency and combined pituitary hormone deficiency
Julia Hoppmann, Denise Rockstroh-Lippold, Peter Gergics, Marilena Nakaguma, Luciani Renata Silveira Carvalho, Heike Pfaeffle, Rami Abou Jamra, Alexander Jorge, Michael H. Guo, Andrew Dauber, Eberhard Keller, Sally A. Camper, Ivo JP Arnhold, Roland Pfaeffle
FC9.2
Contribution of functionally assessed GHRHR mutations to idiopathic isolated Growth Hormone deficiency in a cohort of 312 unrelated patients
Enzo Cohen, Sabrina Belkacem, Soumeya Fedala, Nathalie Collot, Eliane Khallouf, Florence Dastot, Michel Polak, Philippe Duquesnoy, Frederic Brioude, Sophie Rose, Géraldine Viot, Aude Soleyan, Jean-Claude Carel, Marie-Laure Sobrier, Philippe Chanson, Frédérique Gatelais, Claudine Heinrichs, Noureddine Kaffel, Regis Coutant, Şenay Savaş Erdeve, Zehra Aycan, Caroline Thalassinos, Stanislas Lyonnet, Zeynep Şıklar, Merih Berberoglu, Cécile Brachet, Serge Amselem, Marie Legendre
Contribution of functionally assessed GHRHR mutations to idiopathic isolated Growth Hormone deficiency in a cohort of 312 unrelated patients
Enzo Cohen, Sabrina Belkacem, Soumeya Fedala, Nathalie Collot, Eliane Khallouf, Florence Dastot, Michel Polak, Philippe Duquesnoy, Frederic Brioude, Sophie Rose, Géraldine Viot, Aude Soleyan, Jean-Claude Carel, Marie-Laure Sobrier, Philippe Chanson, Frédérique Gatelais, Claudine Heinrichs, Noureddine Kaffel, Regis Coutant, Şenay Savaş Erdeve, Zehra Aycan, Caroline Thalassinos, Stanislas Lyonnet, Zeynep Şıklar, Merih Berberoglu, Cécile Brachet, Serge Amselem, Marie Legendre
FC9.3
Mutations in MAGEL2 and L1CAM are associated with congenital hypopituitarism and arthrogryposis
Louise C Gregory, Shah Pratik, Juliane RF Sanner, Monica Arancibia, Jane Hurst, Wendy D Jones, Helen Spoudeas, Polona Le Quesne Stabej, Louise Ocaka, Carolina Loureiro, Alejandro Martinez-Aguayo, Hywel Williams, Mehul T Dattani
Mutations in MAGEL2 and L1CAM are associated with congenital hypopituitarism and arthrogryposis
Louise C Gregory, Shah Pratik, Juliane RF Sanner, Monica Arancibia, Jane Hurst, Wendy D Jones, Helen Spoudeas, Polona Le Quesne Stabej, Louise Ocaka, Carolina Loureiro, Alejandro Martinez-Aguayo, Hywel Williams, Mehul T Dattani
FC9.4
Neuroendocrine morbidity after Paediatric Craniopharyngioma:a longitudinal single centre analysis of 93 patients over 30 years
Shiraz Dehalvi, Chiara Guzzetti, Hoong-Wei Gan, Helen Spoudeas
Neuroendocrine morbidity after Paediatric Craniopharyngioma:a longitudinal single centre analysis of 93 patients over 30 years
Shiraz Dehalvi, Chiara Guzzetti, Hoong-Wei Gan, Helen Spoudeas
FC9.5
National multidisciplinary decision-making guideline for children and young people (<19 years) with idiopathic thickened pituitary stalk and/or idiopathic central diabetes insipidus
Manuela Cerbone, Chloe Bulwer, Ashraf Ederies, Kirtana Vallabhaneni, Stephen Ball, Ian Kamaly, Ashley Grossman, Helena Gleeson, Marta Korbonits, Vasanta Nanduri, Vaya Tziaferi, Tom Jacques, Johannes Visser, Helen A Spoudeas
National multidisciplinary decision-making guideline for children and young people (<19 years) with idiopathic thickened pituitary stalk and/or idiopathic central diabetes insipidus
Manuela Cerbone, Chloe Bulwer, Ashraf Ederies, Kirtana Vallabhaneni, Stephen Ball, Ian Kamaly, Ashley Grossman, Helena Gleeson, Marta Korbonits, Vasanta Nanduri, Vaya Tziaferi, Tom Jacques, Johannes Visser, Helen A Spoudeas
HA1
EAP1 mutations cause an impaired transcriptional activity on GnRH promoter that leads to self-limited delayed puberty
Alessandra Mancini, Sasha R. Howard, Claudia P. Cabrera, Michael R. Barnes, Sabine Heger, Leonardo Guasti, Sergio Ojeda, Leo Dunkel
EAP1 mutations cause an impaired transcriptional activity on GnRH promoter that leads to self-limited delayed puberty
Alessandra Mancini, Sasha R. Howard, Claudia P. Cabrera, Michael R. Barnes, Sabine Heger, Leonardo Guasti, Sergio Ojeda, Leo Dunkel
LB-P18
The efficacy of GnRHa alone or in combination with rhGH for the treatment of idiopathic central precocious puberty or early and fast puberty in Chinese girls
jianwei zhang, junfen fu
The efficacy of GnRHa alone or in combination with rhGH for the treatment of idiopathic central precocious puberty or early and fast puberty in Chinese girls
jianwei zhang, junfen fu
LB-P6
Sex hormone levels in young children: a pilot study of the Japan Environment and Children’s Study
Tadayuki Ayabe, Maki Fukami, Kiwako Yamamoto-Hanada, Kazue Ishitsuka, Hidetoshi Mezawa, Mizuho Konishi, Mayako Saito, Hatoko Sasaki, Miori Satoh, Minaho Nishizato, Takehiro Michikawa, Shin Yamazaki, Yukifumi Monden, Nathan Mise, Fujio Kayama, Masayuki Shimono, Koichi Kusuhara, Toshihiro Kawamoto, Masafumi Sanefuji, Kiyoko Kato, Masako Oda, Hiroshi Mitsubuchi, Takahiko Katoh, Hirohisa Saito, Yukihiro Ohya
Sex hormone levels in young children: a pilot study of the Japan Environment and Children’s Study
Tadayuki Ayabe, Maki Fukami, Kiwako Yamamoto-Hanada, Kazue Ishitsuka, Hidetoshi Mezawa, Mizuho Konishi, Mayako Saito, Hatoko Sasaki, Miori Satoh, Minaho Nishizato, Takehiro Michikawa, Shin Yamazaki, Yukifumi Monden, Nathan Mise, Fujio Kayama, Masayuki Shimono, Koichi Kusuhara, Toshihiro Kawamoto, Masafumi Sanefuji, Kiyoko Kato, Masako Oda, Hiroshi Mitsubuchi, Takahiko Katoh, Hirohisa Saito, Yukihiro Ohya
LB-P9
Two siblings with autosomal recessive syndromic hypopituitarism caused by mutations in TBC1D32
Johanna Hietamäki, Anna-Pauliina Iivonen, Johanna Känsäkoski, Päivi J. Miettinen, Xiaonan Liu, Kirsi Vaaralahti, Matti Hero, Markku Varjosalo, Taneli Raivio
Two siblings with autosomal recessive syndromic hypopituitarism caused by mutations in TBC1D32
Johanna Hietamäki, Anna-Pauliina Iivonen, Johanna Känsäkoski, Päivi J. Miettinen, Xiaonan Liu, Kirsi Vaaralahti, Matti Hero, Markku Varjosalo, Taneli Raivio
P1-P194
A 7-year update report of a national, interdisciplinary endeavour to improve outcomes for children and young people under 19years of age with hypothalamic pituitary axis tumours(HPAT)using multi-site video conferencing
Katja Freund, Neha Malhorta, Antonia Dastamani, Neil Dorward, Kristian Aquilina, Yen-Ching Chang, Kshitij Mankad, Benedetta Pettorini, Jo Blair J6, Ian Kamaly, Peter E Clayton, Darren Hargrave, Marta Korbonits, Helen A Spoudeas
A 7-year update report of a national, interdisciplinary endeavour to improve outcomes for children and young people under 19years of age with hypothalamic pituitary axis tumours(HPAT)using multi-site video conferencing
Katja Freund, Neha Malhorta, Antonia Dastamani, Neil Dorward, Kristian Aquilina, Yen-Ching Chang, Kshitij Mankad, Benedetta Pettorini, Jo Blair J6, Ian Kamaly, Peter E Clayton, Darren Hargrave, Marta Korbonits, Helen A Spoudeas
P1-P195
Long term reversibility of Presumed ACTH Deficiency (ACTHd) in children and young people (CYP) with Intracranial Germ Cell Tumours (IGCT)
Kyriaki Pieri, Maria Michaelidou, Zaynab Chatoo, Ross Holloway, Antonia Dastamani, Helen A Spoudeas
Long term reversibility of Presumed ACTH Deficiency (ACTHd) in children and young people (CYP) with Intracranial Germ Cell Tumours (IGCT)
Kyriaki Pieri, Maria Michaelidou, Zaynab Chatoo, Ross Holloway, Antonia Dastamani, Helen A Spoudeas
P1-P196
Endocrine follow-up of children with a history of brain tumour. Data from our large cohort at Necker University Hospital, Paris, 2010-2015
Laura Gabriela González Briceño, Dinane Samara-Boustani, Jacques Beltrand, Jacques Grill, Stéphanie Puget, Christelle Dufour, Christian Sainte-Rose, Claire Alapetite, Graziella Pinto, Philippe Touraine, Dominique Valteau-Couant, Dulanjalee Kariyawasam, Isabelle Aerts, Kevin Beccaria, Marie Bourgeois, Thomas Roujeau, Thomas Blauwblomme, Federico Di Rocco, Caroline Thalassinos, Michel Zerah, Christian Pauwels, Laurence Brugières, Syril James, Kanetee Busiah, Albane Simon, Franck Bourdeaut, Stéphanie Bolle, Brice Fresneau, Jean Michon, Daniel Orbach, Léa Guerrini-Rousseau, François Doz, Michel Polak
Endocrine follow-up of children with a history of brain tumour. Data from our large cohort at Necker University Hospital, Paris, 2010-2015
Laura Gabriela González Briceño, Dinane Samara-Boustani, Jacques Beltrand, Jacques Grill, Stéphanie Puget, Christelle Dufour, Christian Sainte-Rose, Claire Alapetite, Graziella Pinto, Philippe Touraine, Dominique Valteau-Couant, Dulanjalee Kariyawasam, Isabelle Aerts, Kevin Beccaria, Marie Bourgeois, Thomas Roujeau, Thomas Blauwblomme, Federico Di Rocco, Caroline Thalassinos, Michel Zerah, Christian Pauwels, Laurence Brugières, Syril James, Kanetee Busiah, Albane Simon, Franck Bourdeaut, Stéphanie Bolle, Brice Fresneau, Jean Michon, Daniel Orbach, Léa Guerrini-Rousseau, François Doz, Michel Polak
P1-P197
A single centre experience of managing a series of childhood macro/giant-prolactinoma
Antonia Dastamani, Chloe Bulwer, Adhraf Ederies, Owase Jeelani, Naomi Fersht, Kristian Aquilina, Marta Korbonits, Helen Spoudeas
A single centre experience of managing a series of childhood macro/giant-prolactinoma
Antonia Dastamani, Chloe Bulwer, Adhraf Ederies, Owase Jeelani, Naomi Fersht, Kristian Aquilina, Marta Korbonits, Helen Spoudeas
P1-P198
A national UK guideline for managing pituitary adenomas in children and young people under 19 years developed according to the AGREE II framework
Jo Blair, Márta Korbonits, Amy Ronaldson, Mary N. Dang, Helen Spoudeas
A national UK guideline for managing pituitary adenomas in children and young people under 19 years developed according to the AGREE II framework
Jo Blair, Márta Korbonits, Amy Ronaldson, Mary N. Dang, Helen Spoudeas
P1-P199
Growth hormone deficiency and cryptorchidism in a family with Xq26.3 duplication and position effect on SOX3
Felix Reschke, Arne Jahn, Andreas Tzschach, Jens Schallner, Maja von der Hagen, Angela Huebner
Growth hormone deficiency and cryptorchidism in a family with Xq26.3 duplication and position effect on SOX3
Felix Reschke, Arne Jahn, Andreas Tzschach, Jens Schallner, Maja von der Hagen, Angela Huebner
P1-P200
PROKR2 mutations in patients with Growth Hormone Deficiency and Multiple Pituitary Hormone Deficiency
Adam Najaflı, Firdevs Baş, Birsen Karaman, Aslı Derya Kardelen Al, Güven Toksoy, Şükran Poyrazoğlu, Oya Uyguner, Şahin Avcı, Umut Altunoğlu, Esin Karakılıç Özturan, Seher Başarn, Feyza Darendeliler
PROKR2 mutations in patients with Growth Hormone Deficiency and Multiple Pituitary Hormone Deficiency
Adam Najaflı, Firdevs Baş, Birsen Karaman, Aslı Derya Kardelen Al, Güven Toksoy, Şükran Poyrazoğlu, Oya Uyguner, Şahin Avcı, Umut Altunoğlu, Esin Karakılıç Özturan, Seher Başarn, Feyza Darendeliler
P1-P201
Anastrozole is safe as monotherapy in early maturing girls with compromised growth, further improving gain in predicted adult height by the initial combination therapy of an LHRH analogue and an aromatase inhibitor. Results from the “GAIL” study ISRCTN11469487
Eleni Dermitzaki, Kleanthis Kleanthous, Maria Papagianni, Achilleas Attilakos, George Mastorakos, Anastasios Papadimitriou, Dimitrios T. Papadimitriou
Anastrozole is safe as monotherapy in early maturing girls with compromised growth, further improving gain in predicted adult height by the initial combination therapy of an LHRH analogue and an aromatase inhibitor. Results from the “GAIL” study ISRCTN11469487
Eleni Dermitzaki, Kleanthis Kleanthous, Maria Papagianni, Achilleas Attilakos, George Mastorakos, Anastasios Papadimitriou, Dimitrios T. Papadimitriou
P1-P202
Long-acting octeotride treatment in children with Neurofibromatosis Type 1 - optic pathway tumors and growth hormone excess
Paula Ximena Molina Guiraldo, Hector Salvador Hernandez, Joan Prat Bartomeu, Casano Sancho Paula
Long-acting octeotride treatment in children with Neurofibromatosis Type 1 - optic pathway tumors and growth hormone excess
Paula Ximena Molina Guiraldo, Hector Salvador Hernandez, Joan Prat Bartomeu, Casano Sancho Paula
P1-P203
Serum concentrations of the endocrine disruptors-organochlorine pesticides (OCPs) in Greek children with Neurodevelopmental Disorders
Gerasimos Makris, George Chrousos, Shaun Sabico, Sherif Abd-Alrahman, Nasser Al-Daghri, George Chouliaras, Panagiota Pervanidou
Serum concentrations of the endocrine disruptors-organochlorine pesticides (OCPs) in Greek children with Neurodevelopmental Disorders
Gerasimos Makris, George Chrousos, Shaun Sabico, Sherif Abd-Alrahman, Nasser Al-Daghri, George Chouliaras, Panagiota Pervanidou
P1-P204
Whole-exome sequencing identifies novel pathogenic variants in Korean families with central precocious puberty
Hae Sang Lee, Jin Soon Hwang
Whole-exome sequencing identifies novel pathogenic variants in Korean families with central precocious puberty
Hae Sang Lee, Jin Soon Hwang
P1-P205
A paternally inherited familial precocious puberty caused by a novel MKRN3 frameshift variant
Jessica Odone, Rachel Nicholls, Kumar Yadlapalli, Elizabeth Crowne, Richard Turnpenny
A paternally inherited familial precocious puberty caused by a novel MKRN3 frameshift variant
Jessica Odone, Rachel Nicholls, Kumar Yadlapalli, Elizabeth Crowne, Richard Turnpenny
P1-P206
MKRN3 levels in girls with central precocious puberty during GnRHa treatment: a longitudinal study
anna grandone, grazia cirillo, marcella sasso, caterina luongo, gianluca tornese, adalgisa festa, emanuele miraglia del giudice
MKRN3 levels in girls with central precocious puberty during GnRHa treatment: a longitudinal study
anna grandone, grazia cirillo, marcella sasso, caterina luongo, gianluca tornese, adalgisa festa, emanuele miraglia del giudice
P1-P207
Urinary Gonadotropins as a useful non-invasive marker of Central Precocious Puberty
Il Tae Hwang, Hwal Rim Jeong, Seung Yang, Young Suk Shim Young Suk Shim
Urinary Gonadotropins as a useful non-invasive marker of Central Precocious Puberty
Il Tae Hwang, Hwal Rim Jeong, Seung Yang, Young Suk Shim Young Suk Shim
P1-P208
Testicular development and puberty in boys with Duchenne Muscular Dystrophy: results from the ScOT-DMD Study
M Denker, S Joseph, M DiMarco, J Dunne, I Horrocks, SF Ahmed, SC Wong
Testicular development and puberty in boys with Duchenne Muscular Dystrophy: results from the ScOT-DMD Study
M Denker, S Joseph, M DiMarco, J Dunne, I Horrocks, SF Ahmed, SC Wong
P1-P209
Exposure to BPA and phthalates and timing of puberty in girls
Annalisa Deodati, Giorgia Bottaro, Sabrina Tait, Francesca Maranghi, Luca Busani, Cinzia La Rocca, Roberta Tassinari, Fabrizia Carli, Veronica Della Latta, Emma Buzzigoli, Amalia Gastaldelli, Stefano Cianfarani
Exposure to BPA and phthalates and timing of puberty in girls
Annalisa Deodati, Giorgia Bottaro, Sabrina Tait, Francesca Maranghi, Luca Busani, Cinzia La Rocca, Roberta Tassinari, Fabrizia Carli, Veronica Della Latta, Emma Buzzigoli, Amalia Gastaldelli, Stefano Cianfarani
P1-P210
Hypothalamic-pituitary-testicular axis response to sub-maximal aerobic exercise, in pre- and early- pubertal normal weight and obese boys
George Paltoglou, Alexandra Avloniti, Athanasios Chatzinikolaou, Aimilia Mantzou, Charikleia Stefanaki, Maria Papagianni, Ioannis Fatouros, Ge Mastorakos
Hypothalamic-pituitary-testicular axis response to sub-maximal aerobic exercise, in pre- and early- pubertal normal weight and obese boys
George Paltoglou, Alexandra Avloniti, Athanasios Chatzinikolaou, Aimilia Mantzou, Charikleia Stefanaki, Maria Papagianni, Ioannis Fatouros, Ge Mastorakos
P1-P211
Effect of pubertal blockade and cross-sex hormone treatment on the growth spurt in young transgender adolescents: a first report.
Matteo Catanzano, Gary Butler
Effect of pubertal blockade and cross-sex hormone treatment on the growth spurt in young transgender adolescents: a first report.
Matteo Catanzano, Gary Butler
P1-P212
Real-world safety data in a cohort of children with Noonan Syndrome treated with Growth Hormone: final results from NordiNet® International Outcome Study (IOS) and ANSWER Program
Pétur Benedikt Júlíusson, Jovanna Dahlgren, M. Jennifer Abuzzahab, Birgitte Tønnes Pedersen, Sebastian Roehrich, Alicia Romano
Real-world safety data in a cohort of children with Noonan Syndrome treated with Growth Hormone: final results from NordiNet® International Outcome Study (IOS) and ANSWER Program
Pétur Benedikt Júlíusson, Jovanna Dahlgren, M. Jennifer Abuzzahab, Birgitte Tønnes Pedersen, Sebastian Roehrich, Alicia Romano
P2-P301
Efficacy and safety of triptorelin 3-monthformulationin patients with centralprecocious puberty and BMI evaluation.
Francesca Galli, Paolo Cavarzere, Sarah Dal Ben, Franco Antoniazzi, Rossella Gaudino
Efficacy and safety of triptorelin 3-monthformulationin patients with centralprecocious puberty and BMI evaluation.
Francesca Galli, Paolo Cavarzere, Sarah Dal Ben, Franco Antoniazzi, Rossella Gaudino
P2-P302
Triptorelin test in idagnosing Central Precocious Puberty
Rade Vukovic, Tatjana Milenkovic, Katarina Mitrovic, Sladjana Todorovic, Ljiljana Plavsic, Ivan Soldatovic
Triptorelin test in idagnosing Central Precocious Puberty
Rade Vukovic, Tatjana Milenkovic, Katarina Mitrovic, Sladjana Todorovic, Ljiljana Plavsic, Ivan Soldatovic
P2-P303
Foot length growth is a novel marker of early puberty
Ben Balzer, Hoi Lun Cheng, Frances Garden, Georgina Luscombe, Karen Paxton, Catherine Hawke, David Handelsman, Katharine Steinbeck
Foot length growth is a novel marker of early puberty
Ben Balzer, Hoi Lun Cheng, Frances Garden, Georgina Luscombe, Karen Paxton, Catherine Hawke, David Handelsman, Katharine Steinbeck
P2-P304
Ultrasound-based measurements of testicular volume in 6-16 year old boys: intra- and inter-observer agreement and comparison with Prader orchidometry
Ninnie Oehme, Mathieu Roelants, Ingvild Særvold Bruserud, Geir Egil Eide, Robert Bjerknes, Karen Rosendahl, Pétur B. Júlíusson
Ultrasound-based measurements of testicular volume in 6-16 year old boys: intra- and inter-observer agreement and comparison with Prader orchidometry
Ninnie Oehme, Mathieu Roelants, Ingvild Særvold Bruserud, Geir Egil Eide, Robert Bjerknes, Karen Rosendahl, Pétur B. Júlíusson
P2-P305
Gonadotropins and free testosterone in obese adolescents: relationship to depressive symptoms
Alaa Youssef Ahmed Baioumi, Noha Refaat Mohamed, Nahla El Sawy, Eman Amin Abd Elaziz
Gonadotropins and free testosterone in obese adolescents: relationship to depressive symptoms
Alaa Youssef Ahmed Baioumi, Noha Refaat Mohamed, Nahla El Sawy, Eman Amin Abd Elaziz
P2-P306
Longitudinal follow-up to near final height of auxological changes in girls with idiopathic central precocious puberty treated with gonadotropin-releasing hormone analog and grouped by pretreatment body mass index level
Jongho Park, Yong-Dae Kim, Heon-Seok Han
Longitudinal follow-up to near final height of auxological changes in girls with idiopathic central precocious puberty treated with gonadotropin-releasing hormone analog and grouped by pretreatment body mass index level
Jongho Park, Yong-Dae Kim, Heon-Seok Han
P2-P307
The effect of GnRH-analogue therapy on the quality of life of patients with central precocious puberty and their families
Laura Lucaccioni, Marisa Pugliese, Elena Manzotti, Patrizia Bruzzi, Beatrice Righi, Silvia Poluzzi, Simona F. Madeo, Elena Bigi, Barbara Predieri, Lorenzo Iughetti
The effect of GnRH-analogue therapy on the quality of life of patients with central precocious puberty and their families
Laura Lucaccioni, Marisa Pugliese, Elena Manzotti, Patrizia Bruzzi, Beatrice Righi, Silvia Poluzzi, Simona F. Madeo, Elena Bigi, Barbara Predieri, Lorenzo Iughetti
P2-P308
A novel inactivating compound heterozygous mutation in KISS1R/GPR54: cases of three siblings
Ozlem Nalbantoglu, Gulcin Arslan, Ozge Koprulu, Fılız Hazan, Semra Gursoy, Behzat Ozkan
A novel inactivating compound heterozygous mutation in KISS1R/GPR54: cases of three siblings
Ozlem Nalbantoglu, Gulcin Arslan, Ozge Koprulu, Fılız Hazan, Semra Gursoy, Behzat Ozkan
P2-P309
MKRN3 gene mutations in a cohort of patients with central precocious puberty
Magdalena Avbelj Stefanija, Jernej Kovač, Galia Yablonski, Alma Toromanović, Gordana Stipančič, Tatjana Milenković, Aleksandra Jančevska, Vera Zdravković, Maja Jesić, Rade Vuković, Sandra Stanković, Slađana Todorović, Tinka Hovnik, Moshe Phillip, Tadej Battelino, Liat de Vries
MKRN3 gene mutations in a cohort of patients with central precocious puberty
Magdalena Avbelj Stefanija, Jernej Kovač, Galia Yablonski, Alma Toromanović, Gordana Stipančič, Tatjana Milenković, Aleksandra Jančevska, Vera Zdravković, Maja Jesić, Rade Vuković, Sandra Stanković, Slađana Todorović, Tinka Hovnik, Moshe Phillip, Tadej Battelino, Liat de Vries
P2-P31
Incidence of delayed puberty in adolescents. A population-based study in a county in central Sweden
Maria Rodanaki, Eva Rask, Maria Lodefalk
Incidence of delayed puberty in adolescents. A population-based study in a county in central Sweden
Maria Rodanaki, Eva Rask, Maria Lodefalk
P2-P310
Can basal levels of luteinizing hormone (LH) replace the GnRH test in the diagnosis of precocious puberty in girls?
Juan Llano, William Morales, Catherine Pineda, Teresa Ortiz, Nayibe Gil, Gladys Laverde, Sonia Castro, Mauricio Llano
Can basal levels of luteinizing hormone (LH) replace the GnRH test in the diagnosis of precocious puberty in girls?
Juan Llano, William Morales, Catherine Pineda, Teresa Ortiz, Nayibe Gil, Gladys Laverde, Sonia Castro, Mauricio Llano
P2-P312
Ultrasound assessment of pubertal breast development: Intra- and inter-observer agreement
Ingvild Bruserud, Roelants Mathieu, Ninnie Oehme, Geir Egil Eide, Robert Bjerknes, Karen Rosendahl, Pétur Júíliusson
Ultrasound assessment of pubertal breast development: Intra- and inter-observer agreement
Ingvild Bruserud, Roelants Mathieu, Ninnie Oehme, Geir Egil Eide, Robert Bjerknes, Karen Rosendahl, Pétur Júíliusson
P2-P313
Neuroendocrine consequences of Hypothalamic Hamartoma and their imaging (MRI) and surgery correlates
Beatriz Corredor, Elisabetta Caredda, Ash Ederies, Martin Tisdall, Helen Cross, Helen A Spoudeas
Neuroendocrine consequences of Hypothalamic Hamartoma and their imaging (MRI) and surgery correlates
Beatriz Corredor, Elisabetta Caredda, Ash Ederies, Martin Tisdall, Helen Cross, Helen A Spoudeas
P2-P314
The start predictors of puberty in boys with constitutional delay of puberty
Liubov Brzhezinskaia, Lyubov Samsonova, Oleg Latyshev, Goar Okminyan, Elena Kiseleva, Elvira Kasatkina
The start predictors of puberty in boys with constitutional delay of puberty
Liubov Brzhezinskaia, Lyubov Samsonova, Oleg Latyshev, Goar Okminyan, Elena Kiseleva, Elvira Kasatkina
P2-P315
Research on the relationship between secular trends of pubertal development and obesity in child and adolescent
Feng Xiong, Xuan Luo, Cui Song, Gao-Hui Zhu, Min Zhu
Research on the relationship between secular trends of pubertal development and obesity in child and adolescent
Feng Xiong, Xuan Luo, Cui Song, Gao-Hui Zhu, Min Zhu
P2-P316
Gonadotropin Levels And Frequency Of Testosterone Supplementation In Adolescents With Klinefelter Syndrome
XANTHIPPI TSERETOPOULOU, TALAT MUSHTAQ
Gonadotropin Levels And Frequency Of Testosterone Supplementation In Adolescents With Klinefelter Syndrome
XANTHIPPI TSERETOPOULOU, TALAT MUSHTAQ
P2-P317
The effect of Letrozole on the reproductive function and linear growth in the early and mid puberty boys
Huamei MA, Juan LIN, Jun ZHANG, Yanhong LI, Qiuli CHEN, Minlian DU
The effect of Letrozole on the reproductive function and linear growth in the early and mid puberty boys
Huamei MA, Juan LIN, Jun ZHANG, Yanhong LI, Qiuli CHEN, Minlian DU
P2-P318
SOX3 gene duplication associated with midline CNS malformations, hypopituitarism and neurodevelopmental abnormalities: 5 unrelated cases
Garima Chawla, Aparna KR Nambisan, Ved B Arya, Nadia Muhi-Iddin, Katia Vamvakiti, Michal Ajzensztejn, Tony Hulse, Charles R Buchanan, Ritika R Kapoor
SOX3 gene duplication associated with midline CNS malformations, hypopituitarism and neurodevelopmental abnormalities: 5 unrelated cases
Garima Chawla, Aparna KR Nambisan, Ved B Arya, Nadia Muhi-Iddin, Katia Vamvakiti, Michal Ajzensztejn, Tony Hulse, Charles R Buchanan, Ritika R Kapoor
P2-P319
An 18 month old boy with hypoglycemic convulsion and obesity due to POMC deficiency
Sare Betul Kaygusuz, Gozde Yesil, Tarık Kırkgoz, Serap Turan, Abdullah Bereket, Tulay Guran
An 18 month old boy with hypoglycemic convulsion and obesity due to POMC deficiency
Sare Betul Kaygusuz, Gozde Yesil, Tarık Kırkgoz, Serap Turan, Abdullah Bereket, Tulay Guran
P2-P320
Pituitary stalk interruption syndrome (PSIS) is not a rare cause of the congenital hypopituitarism
Erdal Eren, Zeynep Yazici, Ozgecan Demirbas, Nadide Basak Gulleroglu, Omer Tarım
Pituitary stalk interruption syndrome (PSIS) is not a rare cause of the congenital hypopituitarism
Erdal Eren, Zeynep Yazici, Ozgecan Demirbas, Nadide Basak Gulleroglu, Omer Tarım
P2-P321
Pallister Hall syndrome: an unusual case of central precocious puberty, prolonged vaginal bleeding, gelastic seizures and polysyndactyly in a 3 month old infant.
Larry Arciniegas, Beatriz Iglesias, Ariadna Campos, Fermina Lopez, Angel Sánchez Montañez, Maria Clemente
Pallister Hall syndrome: an unusual case of central precocious puberty, prolonged vaginal bleeding, gelastic seizures and polysyndactyly in a 3 month old infant.
Larry Arciniegas, Beatriz Iglesias, Ariadna Campos, Fermina Lopez, Angel Sánchez Montañez, Maria Clemente
P2-P322
Primary empty Sella Syndrome and Clnical Endocrine Polymorphisms in children: a report of 15 cases
SIMON KAYEMBA-KAY'S, ALICE RIBRAULT, Prof. PETER HINDMARSH
Primary empty Sella Syndrome and Clnical Endocrine Polymorphisms in children: a report of 15 cases
SIMON KAYEMBA-KAY'S, ALICE RIBRAULT, Prof. PETER HINDMARSH
P2-P323
Growth hormone deficiency (GHD) in a patient with persistence of the craniopharyngeal canal with cephalocele
Silvana Caiulo, Marco Pitea, Cristina Partenope, Dario Gallo, Chiara Damia, Marta Adavastro, Lorenzo Fioretti, Graziano Barera, Giovanna Weber, Gabriella Pozzobon
Growth hormone deficiency (GHD) in a patient with persistence of the craniopharyngeal canal with cephalocele
Silvana Caiulo, Marco Pitea, Cristina Partenope, Dario Gallo, Chiara Damia, Marta Adavastro, Lorenzo Fioretti, Graziano Barera, Giovanna Weber, Gabriella Pozzobon
P2-P324
Endocrine-metabolic characterization of pediatric patients with craniopharyngioma. A single-centre cohort study.
Stefania Pedicelli, Giulia Sette, Stefano Cianfarani, Marco Cappa
Endocrine-metabolic characterization of pediatric patients with craniopharyngioma. A single-centre cohort study.
Stefania Pedicelli, Giulia Sette, Stefano Cianfarani, Marco Cappa
P2-P325
Growth Hormone (GH) secreting pituitary adenomas in paediatric practice: 5 cases over 20 years in a single tertiary NeuroEndocrine Centre
Elspeth Brooker, Sarrah El Munshid, Ved Arya, Jennifer Kalitsi, Dunia Ismail, Ritika Kapoor, Peter Bullock, Nick Thomas, Henry Mandeville, Simon AYLWIN, Charles Buchanan
Growth Hormone (GH) secreting pituitary adenomas in paediatric practice: 5 cases over 20 years in a single tertiary NeuroEndocrine Centre
Elspeth Brooker, Sarrah El Munshid, Ved Arya, Jennifer Kalitsi, Dunia Ismail, Ritika Kapoor, Peter Bullock, Nick Thomas, Henry Mandeville, Simon AYLWIN, Charles Buchanan
P2-P326
Pituitary adenomas in children and adolescents: a retrospective single-centre analysis
Thomas Breil, Catherine Lorz, Daniela Choukair, Janna Mittnacht, Ioana Inta, Daniela Klose, Jessica Jesser, Egbert Schulze, Markus Bettendorf
Pituitary adenomas in children and adolescents: a retrospective single-centre analysis
Thomas Breil, Catherine Lorz, Daniela Choukair, Janna Mittnacht, Ioana Inta, Daniela Klose, Jessica Jesser, Egbert Schulze, Markus Bettendorf
P2-P327
Changes of body composition of male adolescents with GH deficiency are diagnostic during transition
Gerhard Binder, Bettina Becker, Jana Leonie Bauer, Roland Schweizer
Changes of body composition of male adolescents with GH deficiency are diagnostic during transition
Gerhard Binder, Bettina Becker, Jana Leonie Bauer, Roland Schweizer
P2-P328
AMH and Inhibin B level in girls with central precocious puberty
Hwal Rim Jeong, Il Tae Hwang, Kyung Hee Yi
AMH and Inhibin B level in girls with central precocious puberty
Hwal Rim Jeong, Il Tae Hwang, Kyung Hee Yi
P2-P329
Gender-related differences in etiological distribution of organic causes of central precocious puberty
Dogus Vuralli, Alev Ozon, Nazli Gonc, Nurgun Kandemir, Ayfer Alikasifoglu
Gender-related differences in etiological distribution of organic causes of central precocious puberty
Dogus Vuralli, Alev Ozon, Nazli Gonc, Nurgun Kandemir, Ayfer Alikasifoglu
P2-P330
Final adult height in girls with idiopathic central precocious puberty treated with monthly leuprorelin acetate VS triptorelin acetate
Voraluck Phatarakijnirund, Nawaporn Numbenjapon, Chula Kooanantkul, Kwanjai Thanakitcharu, Phairuch Chaiyakul, Karusart Phowang
Final adult height in girls with idiopathic central precocious puberty treated with monthly leuprorelin acetate VS triptorelin acetate
Voraluck Phatarakijnirund, Nawaporn Numbenjapon, Chula Kooanantkul, Kwanjai Thanakitcharu, Phairuch Chaiyakul, Karusart Phowang
P2-P331
The impact of Central Precious Puberty on health-relatedqualityoflifeand social, emotive and behavioral competences among children treated with GnRHa.
Francesca Galli, Paolo Cavarzere, Sarah Dal Ben, Franco Antoniazzi, Rossella Gaudino
The impact of Central Precious Puberty on health-relatedqualityoflifeand social, emotive and behavioral competences among children treated with GnRHa.
Francesca Galli, Paolo Cavarzere, Sarah Dal Ben, Franco Antoniazzi, Rossella Gaudino
P2-P332
Basal and GnRH analog-stimulated peak LH levels for diagnosing girls with early phase of Central Precocious Puberty
Somboon Wankanit, Preamrudee Poomthavorn, Pat Mahachoklertwattana
Basal and GnRH analog-stimulated peak LH levels for diagnosing girls with early phase of Central Precocious Puberty
Somboon Wankanit, Preamrudee Poomthavorn, Pat Mahachoklertwattana
P2-P333
Determination of urinary metabolic profiles of children with central and peripheral precocious puberty
Aylin Balcı, Tuba Reçber, Emirhan Nemutlu, Derya Buluş, Sedef Kır, Belma Koçer Gümüşel, Pınar Erkekoğlu
Determination of urinary metabolic profiles of children with central and peripheral precocious puberty
Aylin Balcı, Tuba Reçber, Emirhan Nemutlu, Derya Buluş, Sedef Kır, Belma Koçer Gümüşel, Pınar Erkekoğlu
P2-P334
Hypertension during GNRH analogues therapy in a 10-year-old girl
Massimo Barreca, Elena Carboni, Maria Scavone, Laura Giancotti, Roberto Miniero
Hypertension during GNRH analogues therapy in a 10-year-old girl
Massimo Barreca, Elena Carboni, Maria Scavone, Laura Giancotti, Roberto Miniero
P2-P335
The effect of Polychlorinobiphenyls on premature puberty in girls
Raziye Burcu Güven, Samim Özen, Damla Gökşen, Özlem Korkmaz, Şükran Darcan
The effect of Polychlorinobiphenyls on premature puberty in girls
Raziye Burcu Güven, Samim Özen, Damla Gökşen, Özlem Korkmaz, Şükran Darcan
P2-P336
A novel mutation in 5’ untranslation region of Makorin ring finger 3 gene associated with the familial precocious puberty
Wenli Lu, Junqi Wang, Chuanyin Li, Ronggui Hu, Wei Wang
A novel mutation in 5’ untranslation region of Makorin ring finger 3 gene associated with the familial precocious puberty
Wenli Lu, Junqi Wang, Chuanyin Li, Ronggui Hu, Wei Wang
P2-P337
A case of testotoxicosis due to a constitutive mutation of the LH receptor initially presented as a central precocious puberty at 3 years old.
Valérie Porquet-Bordes, Catherine Pienkowski, Nicolas de Roux
A case of testotoxicosis due to a constitutive mutation of the LH receptor initially presented as a central precocious puberty at 3 years old.
Valérie Porquet-Bordes, Catherine Pienkowski, Nicolas de Roux
P3-P284
Infant with osteogenesis imperfecta and panhypopituitarism: a case report
Amin Arliena, Anuar Zaini Azriyanti
Infant with osteogenesis imperfecta and panhypopituitarism: a case report
Amin Arliena, Anuar Zaini Azriyanti
P3-P285
Panhypopituitarism with tall stature diagnosed in a 20 years old boy
Andrea Forrester, Griselda Cecchi, Guadalupe Perez, Luciana Soria, Francisca Masllorens, Sofia Juarez P, M. Constanza Vallone, Magdalena Grassi
Panhypopituitarism with tall stature diagnosed in a 20 years old boy
Andrea Forrester, Griselda Cecchi, Guadalupe Perez, Luciana Soria, Francisca Masllorens, Sofia Juarez P, M. Constanza Vallone, Magdalena Grassi
P3-P286
Post-traumatic hypopituitarism caused by pituitary stalk transection
Anna Ruszała, Małgorzata Wójcik, Andrzej Krystynowicz, Łukasz Wyrobek, Jerzy B. Starzyk
Post-traumatic hypopituitarism caused by pituitary stalk transection
Anna Ruszała, Małgorzata Wójcik, Andrzej Krystynowicz, Łukasz Wyrobek, Jerzy B. Starzyk
P3-P287
Invasive macroprolactinoma with cabergoline induced cerebrospinal fluid rhinorrhoea in childhood
Antonia Dastamani, Ashraf Ederies, Kristian Aquilina, Neil Dorward, Márta Korbonits, Helen Spoudeas
Invasive macroprolactinoma with cabergoline induced cerebrospinal fluid rhinorrhoea in childhood
Antonia Dastamani, Ashraf Ederies, Kristian Aquilina, Neil Dorward, Márta Korbonits, Helen Spoudeas
P3-P288
Bilateral optic nerve hypoplasia revealing septo optic dysplasia or De Morsier syndrome: A case report.
aribi yamina, bensaleh meriem, brakni lila, sellal zoubir, lachkhem aicha, ouldkablia samia
Bilateral optic nerve hypoplasia revealing septo optic dysplasia or De Morsier syndrome: A case report.
aribi yamina, bensaleh meriem, brakni lila, sellal zoubir, lachkhem aicha, ouldkablia samia
P3-P289
Investigating malnutrition among children diagnosed with neuroendocrine tumors receiving chemotherapy in a tertiary care hospital of Pakistan.
Arooj Fatima, Syed Sammar Abbas Zaidi
Investigating malnutrition among children diagnosed with neuroendocrine tumors receiving chemotherapy in a tertiary care hospital of Pakistan.
Arooj Fatima, Syed Sammar Abbas Zaidi
P3-P290
An interesting etiology in childhood Central Diabetes Insipidus HIBERNOMA
Ayça Törel Ergür, Ayla Aslan, Ece Canhilal
An interesting etiology in childhood Central Diabetes Insipidus HIBERNOMA
Ayça Törel Ergür, Ayla Aslan, Ece Canhilal
P3-P291
Neonatal panhypopituitarism with hypoglycemia, edema, inspiratory stridor and cholestasis
Benita Momm, Alexander Nitsch, Elke Hammer
Neonatal panhypopituitarism with hypoglycemia, edema, inspiratory stridor and cholestasis
Benita Momm, Alexander Nitsch, Elke Hammer
P3-P292
MRI changes in time after cranial irradiation, and their relation with pituitary function in survivors of childhood medulloblastoma
C.C.N. van Ommen, L. van Iersel, M.H. Lequin, S.C. Clement, G.O.R. Janssens, A.M. Boot, H.N. Caron, H.L. Claahsen-van der Grinten, B. Granzen, K.S. Han, E.M. Michiels, A.S.P. van Trotsenburg, W.P. Vandertop, D.G. van Vuurden, L.C.M. Kremer, A.Y.N. Schouten- van Meeteren, H.M. van Santen
MRI changes in time after cranial irradiation, and their relation with pituitary function in survivors of childhood medulloblastoma
C.C.N. van Ommen, L. van Iersel, M.H. Lequin, S.C. Clement, G.O.R. Janssens, A.M. Boot, H.N. Caron, H.L. Claahsen-van der Grinten, B. Granzen, K.S. Han, E.M. Michiels, A.S.P. van Trotsenburg, W.P. Vandertop, D.G. van Vuurden, L.C.M. Kremer, A.Y.N. Schouten- van Meeteren, H.M. van Santen
P3-P293
Two identical twins... but not in everything. A difficult diagnosis
Chiara Maria Damia, Dario Gallo, Cristina Partenope, Marco Pitea, Lorenzo Fioretti, Marta Adavastro, Roberta Pajno, Giovanna Weber, Graziano Barera
Two identical twins... but not in everything. A difficult diagnosis
Chiara Maria Damia, Dario Gallo, Cristina Partenope, Marco Pitea, Lorenzo Fioretti, Marta Adavastro, Roberta Pajno, Giovanna Weber, Graziano Barera
P3-P294
Growth hormone deficit associated to complex arteriovenous malformation – case report
Mirela Mogoi, Puiu Iulian Velea, Corina Paul
Growth hormone deficit associated to complex arteriovenous malformation – case report
Mirela Mogoi, Puiu Iulian Velea, Corina Paul
P3-P295
Does Acquired Hypothyroidism Lead to Precocious Puberty?
Dilek Aydın, Pınar İşgüven, Engin Aydın
Does Acquired Hypothyroidism Lead to Precocious Puberty?
Dilek Aydın, Pınar İşgüven, Engin Aydın
P3-P296
Analysis of influencing factors on bone maturation in girls with Central Precocious Puberty (CPP)
Gi-Min Lee, Jung-Eun Moon, Su-Jeong Lee, Hyeon-A Kim, Cheol-Woo Ko
Analysis of influencing factors on bone maturation in girls with Central Precocious Puberty (CPP)
Gi-Min Lee, Jung-Eun Moon, Su-Jeong Lee, Hyeon-A Kim, Cheol-Woo Ko
P3-P297
Is Prematüre Adrenarch Associated With Precocıous Puberty Vıa Kisspeptin?
Aysun Albayrak, Gul Direk, Zeynep Uzan Tatlı, Merve Nur Hepokur, Leyla Akın, Nihal Hatipoğlu, Mustafa Kendirci, Selim Kurtoğlu
Is Prematüre Adrenarch Associated With Precocıous Puberty Vıa Kisspeptin?
Aysun Albayrak, Gul Direk, Zeynep Uzan Tatlı, Merve Nur Hepokur, Leyla Akın, Nihal Hatipoğlu, Mustafa Kendirci, Selim Kurtoğlu
P3-P298
Distinct presentations of McCune Albright syndrome, report of two cases
Gul Yesiltepe Mutlu, Sema Kabataş Eryilmaz, Serdar Ceylaner, Sukru Hatun
Distinct presentations of McCune Albright syndrome, report of two cases
Gul Yesiltepe Mutlu, Sema Kabataş Eryilmaz, Serdar Ceylaner, Sukru Hatun
P3-P301
A case of central diabetes insipidus developed 4 years after the non-CNS-risk unifocal bone lesion of Langerhans cell histiocytosis
Hisae Nakatani, Kentaro Miyai, Kei Takasawa, Kenichi Kashimada, Akira Morimoto, Masayuki Nagasawa, Akihiro Oshiba
A case of central diabetes insipidus developed 4 years after the non-CNS-risk unifocal bone lesion of Langerhans cell histiocytosis
Hisae Nakatani, Kentaro Miyai, Kei Takasawa, Kenichi Kashimada, Akira Morimoto, Masayuki Nagasawa, Akihiro Oshiba
P3-P302
Effect of triptoreline in patients with central precocious puberty at Children’s Hospital 1, Ho Chi Minh City, Vietnam
Loan Huynh, Huyen Tran
Effect of triptoreline in patients with central precocious puberty at Children’s Hospital 1, Ho Chi Minh City, Vietnam
Loan Huynh, Huyen Tran
P3-P303
Morning basal luteinizing hormone, a good screening tool for diagnosing central precocious puberty
In Hyuk Jung, Dong Min Lee
Morning basal luteinizing hormone, a good screening tool for diagnosing central precocious puberty
In Hyuk Jung, Dong Min Lee
P3-P307
Premature adrenarche and pseudohypoparathyroidism – mechanistically linked or coincidence?
Jessica Odone, Kumar Yadlapalli, Christine Burren
Premature adrenarche and pseudohypoparathyroidism – mechanistically linked or coincidence?
Jessica Odone, Kumar Yadlapalli, Christine Burren
P3-P308
Efficacy of Ziyin Xiehuo Granules and Zishen Qinggan Granules in girls with Partial Precocious Puberty:a multicenter, randomized, single-blinded, controlled trial
Wen Sun, Xinhui Han, Jian YU, Yonghong Wang, Weili Yan
Efficacy of Ziyin Xiehuo Granules and Zishen Qinggan Granules in girls with Partial Precocious Puberty:a multicenter, randomized, single-blinded, controlled trial
Wen Sun, Xinhui Han, Jian YU, Yonghong Wang, Weili Yan
P3-P309
GLP-1 receptor agonist in a patient with craniopharyngioma-related obesity.
Maria-Christina Antoniou, Patricia Diaz-Escagedo, Thérèse Bouthors, Eglantine Elowe-Gruau, Sophie Stoppa-Vaucher, Mahmoud Messerer, Michael Hauschild
GLP-1 receptor agonist in a patient with craniopharyngioma-related obesity.
Maria-Christina Antoniou, Patricia Diaz-Escagedo, Thérèse Bouthors, Eglantine Elowe-Gruau, Sophie Stoppa-Vaucher, Mahmoud Messerer, Michael Hauschild
P3-P310
Poland’s syndrome and hypogonadotropic hypogonadism
Marianna Rita Stancampiano, Silvia Laura Carla Meroni, Alessandra Di Lascio, Moira Gianninoto, Gianni Russo
Poland’s syndrome and hypogonadotropic hypogonadism
Marianna Rita Stancampiano, Silvia Laura Carla Meroni, Alessandra Di Lascio, Moira Gianninoto, Gianni Russo
P3-P311
Congenital hypopituitarism associated with complex cranio-vertebral junction anomalies
Mariella Valenzise, Elda Pitrolo, Michele Biasi, Simona Santucci, Malgorzata Wasniewska, Filippo De Luca
Congenital hypopituitarism associated with complex cranio-vertebral junction anomalies
Mariella Valenzise, Elda Pitrolo, Michele Biasi, Simona Santucci, Malgorzata Wasniewska, Filippo De Luca
P3-P312
Premature thelarche followed by acute lymphoblastic leukemia in a 1.5 year old girl
Marina Krstevska-Konstantinova, Ana Stamatova, Konstandina Kuzevska-Maneva, Svetlana Kocheva, Biljana Conevska, Kata Martinova, Aleksandra Jovanovska
Premature thelarche followed by acute lymphoblastic leukemia in a 1.5 year old girl
Marina Krstevska-Konstantinova, Ana Stamatova, Konstandina Kuzevska-Maneva, Svetlana Kocheva, Biljana Conevska, Kata Martinova, Aleksandra Jovanovska
P3-P313
Two cases of non-syndromic congenital unilateral hypoplasia in one family
Ana Stamatova, Konstandina Kuzevska-Maneva, Elena Sukareva-Angelovska, Zoran Gucev, Velibor Tasic, Julija Höfele, Marina Krstevska-Konstantinova
Two cases of non-syndromic congenital unilateral hypoplasia in one family
Ana Stamatova, Konstandina Kuzevska-Maneva, Elena Sukareva-Angelovska, Zoran Gucev, Velibor Tasic, Julija Höfele, Marina Krstevska-Konstantinova
P3-P314
Klinefelter Syndrome with ambiguous genitalia in a child
Muhammad Faizi, Nur Rochmah, Arie Purwana
Klinefelter Syndrome with ambiguous genitalia in a child
Muhammad Faizi, Nur Rochmah, Arie Purwana
P3-P315
The change in growth’s velocity in patients with premature puberty receiving treatment with analogues of lyuliberin
Olga Berseneva, Elena Bashnina, Mariia Turkunova
The change in growth’s velocity in patients with premature puberty receiving treatment with analogues of lyuliberin
Olga Berseneva, Elena Bashnina, Mariia Turkunova
P3-P316
The efficacy of treatment in Vietnamese children with central precocious puberty
Vy Vo Tuong, Luan Nguyen Huy, Quynh Huynh Thi Vu
The efficacy of treatment in Vietnamese children with central precocious puberty
Vy Vo Tuong, Luan Nguyen Huy, Quynh Huynh Thi Vu
P3-P317
The characteristics of central precocious puberty at Children’s Hospital 2 in Vietnam
Quynh Huynh Thi Vu, An Pham Le, Hong Nguyen Thi Minh, Tru Vu Huy
The characteristics of central precocious puberty at Children’s Hospital 2 in Vietnam
Quynh Huynh Thi Vu, An Pham Le, Hong Nguyen Thi Minh, Tru Vu Huy
P3-P318
SIG (Special Interest Group)-ENDOPED/RUTE (Brazil): Seven years integrating pediatric endocrinology centers throughout the country
Ricardo Fernando Arrais, Crésio Aragão Dantas Alves, Gil Guerra Junior, Luiz Claudio Gonçalves Castro, Geraldo Miranda Graça Filho, Cristiane Kopacek, Durval Damiani, Raphael Del Roio Liberatore Junior, Marcia Khaled Puñales
SIG (Special Interest Group)-ENDOPED/RUTE (Brazil): Seven years integrating pediatric endocrinology centers throughout the country
Ricardo Fernando Arrais, Crésio Aragão Dantas Alves, Gil Guerra Junior, Luiz Claudio Gonçalves Castro, Geraldo Miranda Graça Filho, Cristiane Kopacek, Durval Damiani, Raphael Del Roio Liberatore Junior, Marcia Khaled Puñales
P3-P319
The relationship between prolactin and development of puberty in girls with early breast development
Seong Yong Lee
The relationship between prolactin and development of puberty in girls with early breast development
Seong Yong Lee
P3-P320
Central Precocious Puberty appeared in infancy period in a patient of Sotos Syndrome
Tuğba Çetin, Serdar Ceylaner, Zeynep Şıklar, Merih Berberoğlu
Central Precocious Puberty appeared in infancy period in a patient of Sotos Syndrome
Tuğba Çetin, Serdar Ceylaner, Zeynep Şıklar, Merih Berberoğlu
P3-P418
Clinical and Endocrinological Manifestations of Partial Ectopic Posterior Pituitary: A New Imaging Entity
Marina Ybarra, Rawan Hafiz, Marie-Ève Robinson, Julia von Oettingen, Helen Bui, Christine Saint-Martin
Clinical and Endocrinological Manifestations of Partial Ectopic Posterior Pituitary: A New Imaging Entity
Marina Ybarra, Rawan Hafiz, Marie-Ève Robinson, Julia von Oettingen, Helen Bui, Christine Saint-Martin
RFC13.1
Risk of long-term endocrine sequelae in survivors of progressing childhood optic pathway glioma (OPG) treated by upfront chemotherapy. Preliminary analyses of 102 subjects from the French multicentric BB-SFOP registry
Helene Hippolyte, Emilie De Carli, Isabelle Pellier, Matthieu Delion, Josue Rakotonjanahary, Xavier Rialland, Regis Coutant
Risk of long-term endocrine sequelae in survivors of progressing childhood optic pathway glioma (OPG) treated by upfront chemotherapy. Preliminary analyses of 102 subjects from the French multicentric BB-SFOP registry
Helene Hippolyte, Emilie De Carli, Isabelle Pellier, Matthieu Delion, Josue Rakotonjanahary, Xavier Rialland, Regis Coutant
RFC13.2
Growth outcomes and near adult height of children with congenital GH deficiency (GHD) due to abnormal pituitary development: data from a prospective, multinational observational study
Christopher Child, Juliane Leger, Cheri Deal, Imane Benabbad, Nan Jia, Werner Blum
Growth outcomes and near adult height of children with congenital GH deficiency (GHD) due to abnormal pituitary development: data from a prospective, multinational observational study
Christopher Child, Juliane Leger, Cheri Deal, Imane Benabbad, Nan Jia, Werner Blum
RFC13.3
CIRCULATING MKRN3, KISSPEPTIN AND IGF-1 LEVELS IN GIRLS DURING THE CLINICAL ONSET OF PUBERTY.
Lixue Ouyang, Fan Yang
CIRCULATING MKRN3, KISSPEPTIN AND IGF-1 LEVELS IN GIRLS DURING THE CLINICAL ONSET OF PUBERTY.
Lixue Ouyang, Fan Yang
RFC13.4
Gain in predicted adult height using the combination of an LHRH analogue and an aromatase inhibitor in early maturing girls with compromised growth for 2 yrs or until the age of 11 is maintained and further improved by aromatase inhibitor monotherapy. Results on final height of the “GAIL” study ISRCTN11469487
Dimitrios T. Papadimitriou, Eleni Dermitzaki, Maria Papagianni, Kleanthis Kleanthous, Achilleas Attilakos, George Mastorakos, Anastasios Papadimitriou
Gain in predicted adult height using the combination of an LHRH analogue and an aromatase inhibitor in early maturing girls with compromised growth for 2 yrs or until the age of 11 is maintained and further improved by aromatase inhibitor monotherapy. Results on final height of the “GAIL” study ISRCTN11469487
Dimitrios T. Papadimitriou, Eleni Dermitzaki, Maria Papagianni, Kleanthis Kleanthous, Achilleas Attilakos, George Mastorakos, Anastasios Papadimitriou
RFC13.5
Pubertal voice break: temporal relation of secondary sexual characteristics in healthy boys
Alexander Siegfried Busch, Casper P. Hagen, Kaspar Sørensen, Nanna Kolby, Camilla Eckert-Lind, Anders Juul
Pubertal voice break: temporal relation of secondary sexual characteristics in healthy boys
Alexander Siegfried Busch, Casper P. Hagen, Kaspar Sørensen, Nanna Kolby, Camilla Eckert-Lind, Anders Juul
RFC13.6
Close correlation between salivary and blood steroids in normal boys: salivary testosterone best characterizes male puberty
Karl Otfried Schwab, Karoline Dickhuth, Rebekka Mumm, Bernhard Stier, Juergen Doerfer, Dirk Grueninger, Corinna Melanie Brichta, Natascha van der Werf-Grohmann, Michael Wurm, Andreas Krebs
Close correlation between salivary and blood steroids in normal boys: salivary testosterone best characterizes male puberty
Karl Otfried Schwab, Karoline Dickhuth, Rebekka Mumm, Bernhard Stier, Juergen Doerfer, Dirk Grueninger, Corinna Melanie Brichta, Natascha van der Werf-Grohmann, Michael Wurm, Andreas Krebs
RFC9.1
Clinical and genetic features of central precocious puberty associated with complex phenotypes
Ana Canton, Vinicius Brito, Luciana Montenegro, Carolina Ramos, Delanie Macedo, Danielle Bessa, Marina Cunha, Alexander Jorge, Berenice Mendonca, Ana Claudia Latronico
Clinical and genetic features of central precocious puberty associated with complex phenotypes
Ana Canton, Vinicius Brito, Luciana Montenegro, Carolina Ramos, Delanie Macedo, Danielle Bessa, Marina Cunha, Alexander Jorge, Berenice Mendonca, Ana Claudia Latronico
RFC9.2
Novel variant in GNRHR gene regulatory region in a pedigree with maternally inherited precocious puberty
Magdalena Avbelj Stefanija, Jernej Kovač, Galia Yablonski, Moshe Phillip, Tadej Battelino, Liat de Vries
Novel variant in GNRHR gene regulatory region in a pedigree with maternally inherited precocious puberty
Magdalena Avbelj Stefanija, Jernej Kovač, Galia Yablonski, Moshe Phillip, Tadej Battelino, Liat de Vries
RFC9.3
What is the best parameter to decide the initial dose of depot leuprolide acetate in girls with idiopathic central precocious puberty?
Dogus Vuralli, Ayfer Alikasifoglu, Irem Iyigun, Dicle Canoruc, Alev Ozon, Nazli Gonc, Nurgun Kandemir
What is the best parameter to decide the initial dose of depot leuprolide acetate in girls with idiopathic central precocious puberty?
Dogus Vuralli, Ayfer Alikasifoglu, Irem Iyigun, Dicle Canoruc, Alev Ozon, Nazli Gonc, Nurgun Kandemir
RFC9.4
REplacement of MAle mini-Puberty in neonates and children with micropenis and cryptorchidism due to hypogonadotropic hypogonadism. Results of the “REMAP” study ISRCTN13007297
Dimitrios T. Papadimitriou, Dionysios Chrysis, Georgia Nyktari, George Zoupanos, Eleni Liakou, Anastasios Papadimitriou, George Mastorakos
REplacement of MAle mini-Puberty in neonates and children with micropenis and cryptorchidism due to hypogonadotropic hypogonadism. Results of the “REMAP” study ISRCTN13007297
Dimitrios T. Papadimitriou, Dionysios Chrysis, Georgia Nyktari, George Zoupanos, Eleni Liakou, Anastasios Papadimitriou, George Mastorakos
RFC9.5
Non-isolated central precocious puberty: prevalence of brain lesions and other associated disorders
Selmen Wannes, Monique El Maleh, Nicolas De Roux, Delphine Zénaty, Dominique Simon, Laetitia Martinerie, Caroline Storey, Georges Gelwane, Anne Paulsen, Emmanuel Ecosse, Carel Jean-claude, Léger Juliane
Non-isolated central precocious puberty: prevalence of brain lesions and other associated disorders
Selmen Wannes, Monique El Maleh, Nicolas De Roux, Delphine Zénaty, Dominique Simon, Laetitia Martinerie, Caroline Storey, Georges Gelwane, Anne Paulsen, Emmanuel Ecosse, Carel Jean-claude, Léger Juliane
RFC9.6
Can neuroimaging predict endocrine morbidity in Congenital Hypothalamo-pituitary (H-P) disorders?
Manuela Cerbone, Maria Güemes, Angie Wade, Nicola Improda, Mehul T Dattani
Can neuroimaging predict endocrine morbidity in Congenital Hypothalamo-pituitary (H-P) disorders?
Manuela Cerbone, Maria Güemes, Angie Wade, Nicola Improda, Mehul T Dattani
FC10.5
A 5-year single-centre experience on the safety and efficacy of Sirolimus therapy used for the treatment of congenital hyperinsulinaemic hypoglycaemia
Maria Güemes, Antonia Dastamani, Michael Ashworth, Kate Morgan, Sian Ellard, Sarah Flanagan, Mehul Dattani, Pratik Shah
A 5-year single-centre experience on the safety and efficacy of Sirolimus therapy used for the treatment of congenital hyperinsulinaemic hypoglycaemia
Maria Güemes, Antonia Dastamani, Michael Ashworth, Kate Morgan, Sian Ellard, Sarah Flanagan, Mehul Dattani, Pratik Shah
FC7.1
Expression and localisation of insulin, glucagon, amylin, pancreatic polypeptide and PDX-1 in pancreatic tissue of children with congenital hyperinsulinism.
Maria Güemes, Sofia Rahman, Nita Solanky, Clare Gilbert, Kate Morgan, Pratik Shah, Khalid Hussain
Expression and localisation of insulin, glucagon, amylin, pancreatic polypeptide and PDX-1 in pancreatic tissue of children with congenital hyperinsulinism.
Maria Güemes, Sofia Rahman, Nita Solanky, Clare Gilbert, Kate Morgan, Pratik Shah, Khalid Hussain
FC7.2
Enteroinsular hormone responses during fasting, oral glucose tolerance test and mixed meal in children with hyperinsulinaemic hypoglycaemia.
Maria Güemes, Sofia Rahman, Kate Morgan, Clare Gilbert, Pratik Shah, Khalid Hussain
Enteroinsular hormone responses during fasting, oral glucose tolerance test and mixed meal in children with hyperinsulinaemic hypoglycaemia.
Maria Güemes, Sofia Rahman, Kate Morgan, Clare Gilbert, Pratik Shah, Khalid Hussain
FC7.3
Diazoxide-induced pulmonary hypertension: UK multicentre retrospective study on the risk factors, monitoring approach and management recommendations
Suet Ching Chen, Antonia Dastamani, Donatella Pintus, Daphne Yau, Sommayya Aftab, Louise Bath, Craig Swinburne, Lindsey Hunter, Alessandro Giardini, Georgi Christov, Senthil Senniappan, Indraneel Banerjee, Guftar Shaikh, Pratik Shah
Diazoxide-induced pulmonary hypertension: UK multicentre retrospective study on the risk factors, monitoring approach and management recommendations
Suet Ching Chen, Antonia Dastamani, Donatella Pintus, Daphne Yau, Sommayya Aftab, Louise Bath, Craig Swinburne, Lindsey Hunter, Alessandro Giardini, Georgi Christov, Senthil Senniappan, Indraneel Banerjee, Guftar Shaikh, Pratik Shah
FC7.4
Altered substrate specificities and metabolite production by aromatase (CYP19A1) due to the R192H mutation
Sameer S Udhane, Bernhard Dick, Amit V Pandey
Altered substrate specificities and metabolite production by aromatase (CYP19A1) due to the R192H mutation
Sameer S Udhane, Bernhard Dick, Amit V Pandey
LB-P17
Protein-Induced Hypoglycemia Secondary to Hyperinsulinism-Hyperammonemia (HI/HA) Syndrome: a GLUD1 Gene Mutation
Fabiola D'Ambrosio, Ashley Buchanan, Jacquelin Chan, Stelios Mantis
Protein-Induced Hypoglycemia Secondary to Hyperinsulinism-Hyperammonemia (HI/HA) Syndrome: a GLUD1 Gene Mutation
Fabiola D'Ambrosio, Ashley Buchanan, Jacquelin Chan, Stelios Mantis
LB-P5
ASSOCIATION BETWEEN THE USE OF ANTENATAL STEROIDS FOR LUNG MATURATION AND HYPOGLYCEMIA IN NEWBORNS BETWEEN 26 AND 34 6/7 WEEKS OF GESTATION.
Gina Marcela Gonzalez Valencia, Jessica Lorena González Castañeda, María Camila Velandia Avendaño, Fabio Camilo Suarez Cadena, Eliana Rocío Arango Fontecha, Andres Felipe Ochoa Diaz, Victor Clemente Medonza Rojas
ASSOCIATION BETWEEN THE USE OF ANTENATAL STEROIDS FOR LUNG MATURATION AND HYPOGLYCEMIA IN NEWBORNS BETWEEN 26 AND 34 6/7 WEEKS OF GESTATION.
Gina Marcela Gonzalez Valencia, Jessica Lorena González Castañeda, María Camila Velandia Avendaño, Fabio Camilo Suarez Cadena, Eliana Rocío Arango Fontecha, Andres Felipe Ochoa Diaz, Victor Clemente Medonza Rojas
P1-P135
Cardiac and vascular assessments in small- versus appropriate-for-gestational-age infants at ages 1 and 2 years
Cristina Garcia-Beltran, Giorgia Sebastiani, Stella Pie, Alberto Guerra, Abel López-Bermejo, Francis de Zegher, Ferran Rosés, Lourdes Ibáñez
Cardiac and vascular assessments in small- versus appropriate-for-gestational-age infants at ages 1 and 2 years
Cristina Garcia-Beltran, Giorgia Sebastiani, Stella Pie, Alberto Guerra, Abel López-Bermejo, Francis de Zegher, Ferran Rosés, Lourdes Ibáñez
P1-P136
Bone maturation as a predictive factor of catch-up growth during the first year of life in born small for gestational age infants: a prospective study
Giorgia Pepe, Mariarosa Calafiore, Mariella Valenzise, Letteria Morabito, Filippo De Luca, Malgorzata Wasniewska
Bone maturation as a predictive factor of catch-up growth during the first year of life in born small for gestational age infants: a prospective study
Giorgia Pepe, Mariarosa Calafiore, Mariella Valenzise, Letteria Morabito, Filippo De Luca, Malgorzata Wasniewska
P1-P137
Neonatal screening tests in premature newborns in Southern Brasil
Ivy Hulbert Falcão Furtado, Gabriela Carvalho Kraemer, Marcella Rabassi de Lima, Mousseline Torquato Domingos, Rosana Marques Pereira, Monica Nunes Lima Cat, Luiz De Lacerda, Regina Paula Guimarães Vieira Cavalcante da Silva, Ana Lucia Figueiredo Sarquis, Suzana Nesi-França
Neonatal screening tests in premature newborns in Southern Brasil
Ivy Hulbert Falcão Furtado, Gabriela Carvalho Kraemer, Marcella Rabassi de Lima, Mousseline Torquato Domingos, Rosana Marques Pereira, Monica Nunes Lima Cat, Luiz De Lacerda, Regina Paula Guimarães Vieira Cavalcante da Silva, Ana Lucia Figueiredo Sarquis, Suzana Nesi-França
P1-P138
Measurement of estradiol and testosterone in umbilical cord blood by gas chromatography-tandem mass spectrometry (GC-MS/MS); comparisons with radioimmunoassay (RIA)
Kerstin Allvin, Jovanna Dahlgren, Mats X Andersson, Carina Ankarberg-Lindgren
Measurement of estradiol and testosterone in umbilical cord blood by gas chromatography-tandem mass spectrometry (GC-MS/MS); comparisons with radioimmunoassay (RIA)
Kerstin Allvin, Jovanna Dahlgren, Mats X Andersson, Carina Ankarberg-Lindgren
P1-P139
Transient neonatal iatrogenic hypothyroidism due to iodinated contrast
Ulrika Härenstam, Ola Hafström, Annika Reims
Transient neonatal iatrogenic hypothyroidism due to iodinated contrast
Ulrika Härenstam, Ola Hafström, Annika Reims
P1-P140
Sexual dimorphism of IGF1 and IGF2 expression in the neonatal rat brain
Santiago Guerra-Cantero, Marta Torrecilla, Francisca Diaz, Jesús Argente, Julie Chowen
Sexual dimorphism of IGF1 and IGF2 expression in the neonatal rat brain
Santiago Guerra-Cantero, Marta Torrecilla, Francisca Diaz, Jesús Argente, Julie Chowen
P2-P181
Clinical characteristics of congenital hyperinsulinism caused by dominant KCNJ11/ABCC8 mutations.
Maria Melikyan, Diliara Gubaeva, Anatoliy Tyulpakov, Maria Kareva
Clinical characteristics of congenital hyperinsulinism caused by dominant KCNJ11/ABCC8 mutations.
Maria Melikyan, Diliara Gubaeva, Anatoliy Tyulpakov, Maria Kareva
P2-P182
Clinical characterstics, genotype-phenotype correlations and follow up of patients with congenital hyperinsulinaemic hypoglycaemia; single center experience from a southeastern city of Turkey
Mehmet Nuri Ozbek, Huseyin Demirbilek, Belma Haliloglu, Meliha Demiral, Riza Taner Baran, Sian Ellard, Jayne Houghton, Sarah E. Flanagan, Khalid Hussain
Clinical characterstics, genotype-phenotype correlations and follow up of patients with congenital hyperinsulinaemic hypoglycaemia; single center experience from a southeastern city of Turkey
Mehmet Nuri Ozbek, Huseyin Demirbilek, Belma Haliloglu, Meliha Demiral, Riza Taner Baran, Sian Ellard, Jayne Houghton, Sarah E. Flanagan, Khalid Hussain
P2-P183
Congenital Hyperinsulinism: management & outcome in West of Scotland
Khadiga Eltonbary, Peter Robinson, Indi Banerjee, Mohammed Guftar Shaikh
Congenital Hyperinsulinism: management & outcome in West of Scotland
Khadiga Eltonbary, Peter Robinson, Indi Banerjee, Mohammed Guftar Shaikh
P2-P184
20 cases of congenital hyperinsulinism in Ukraine
Evgenia Globa, Nataliya Zelinska, Sian Ellard, Sarah Flanagan, Henrik Christesen
20 cases of congenital hyperinsulinism in Ukraine
Evgenia Globa, Nataliya Zelinska, Sian Ellard, Sarah Flanagan, Henrik Christesen
P2-P185
Nifedipine therapy in hyperinsulinaemic hypoglycaemia due to mutations in the PMM2 gene improves fast tolerance, stabilises blood glucose profile, and enables rationalisation of treatments for glycaemic control and hypertension: the first reported trial in 3 patients in a tertiary centre
Harshini Katugampola, Maria Güemes, Sommayya Aftab, Neha Malhotra, Clare Gilbert, Kate Morgan, Detlef Böckenhauer, Mehul Dattani, Pratik Shah
Nifedipine therapy in hyperinsulinaemic hypoglycaemia due to mutations in the PMM2 gene improves fast tolerance, stabilises blood glucose profile, and enables rationalisation of treatments for glycaemic control and hypertension: the first reported trial in 3 patients in a tertiary centre
Harshini Katugampola, Maria Güemes, Sommayya Aftab, Neha Malhotra, Clare Gilbert, Kate Morgan, Detlef Böckenhauer, Mehul Dattani, Pratik Shah
P2-P186
Potentially modifiable predictors of adverse neonatal outcomes in women with gestational diabetes mellitus (GDM)
Maria-Christina Antoniou, Leah Gilbert, Celine Fischer Fumeaux, Justine Gross, Stefano Lanzi, Yvan Vial, Jardena Puder
Potentially modifiable predictors of adverse neonatal outcomes in women with gestational diabetes mellitus (GDM)
Maria-Christina Antoniou, Leah Gilbert, Celine Fischer Fumeaux, Justine Gross, Stefano Lanzi, Yvan Vial, Jardena Puder
P2-P187
A boy with diazoxide unresponsive congenital hyperinsulinism due to a homozygous ABCC8 missense mutation previously reported to be dominant
Sonya Galcheva, Violeta Iotova, Sarah E. Flanagan, Sian Ellard, Andrew Hattersley
A boy with diazoxide unresponsive congenital hyperinsulinism due to a homozygous ABCC8 missense mutation previously reported to be dominant
Sonya Galcheva, Violeta Iotova, Sarah E. Flanagan, Sian Ellard, Andrew Hattersley
P2-P188
Diazoxide unresponsive Congenital Hyperinsulinism due to a Novel ABCC8 Missense Mutation.
YASMINE OUAREZKI, ASMAHANE LADJOUZE, ADEL DJERMANE, JAYNE HOUGHTON, HACHEMI MAOUCHE, ZOHIR BOUZERAR, YOUCEF TAYEBI
Diazoxide unresponsive Congenital Hyperinsulinism due to a Novel ABCC8 Missense Mutation.
YASMINE OUAREZKI, ASMAHANE LADJOUZE, ADEL DJERMANE, JAYNE HOUGHTON, HACHEMI MAOUCHE, ZOHIR BOUZERAR, YOUCEF TAYEBI
P2-P189
Neonatal hypoglycaemia: unchanged risk of neurodevelopmental impairment, but sex-specific decreased fine motor function and increased internalizing behaviour at school age
Annett Helleskov, Sonja Wehberg, Fani Juel Pørtner, Anna-Marie Larsen, Karen Filipsen, Henrik Thybo Christesen
Neonatal hypoglycaemia: unchanged risk of neurodevelopmental impairment, but sex-specific decreased fine motor function and increased internalizing behaviour at school age
Annett Helleskov, Sonja Wehberg, Fani Juel Pørtner, Anna-Marie Larsen, Karen Filipsen, Henrik Thybo Christesen
P2-P190
Atypical Hepatoblastoma and Wilm’s Tumour in an infant with Beckwith-Wiedemann Syndrome and Diazoxide Resistant Congenital Hyperinsulinism
SAURABH UPPAL, SENTHIL SENNIAPPAN, MOHAMMAD DIDI, JAMES HAYDEN
Atypical Hepatoblastoma and Wilm’s Tumour in an infant with Beckwith-Wiedemann Syndrome and Diazoxide Resistant Congenital Hyperinsulinism
SAURABH UPPAL, SENTHIL SENNIAPPAN, MOHAMMAD DIDI, JAMES HAYDEN
P2-P191
Association between Rubenstein-Taybi Syndrome and hyperinsulinaemic hypoglycaemia
Ranna El-Khairi, Antonia Destamani, Emma Clements, Kate Morgan, Jane Hurst, Pratik Shah
Association between Rubenstein-Taybi Syndrome and hyperinsulinaemic hypoglycaemia
Ranna El-Khairi, Antonia Destamani, Emma Clements, Kate Morgan, Jane Hurst, Pratik Shah
P2-P192
Hyperinsulinemic hypoglycemia in congenital disorder of glycosylation type-1a (CDG-1a)
Dogus Vuralli, Yilmaz Yildiz, H. Serap Sivri, Ayfer Alikasifoglu
Hyperinsulinemic hypoglycemia in congenital disorder of glycosylation type-1a (CDG-1a)
Dogus Vuralli, Yilmaz Yildiz, H. Serap Sivri, Ayfer Alikasifoglu
P2-P193
A rare cause of hyperinsulinemic hypoglycemia: Costello syndrome
Dogus Vuralli, Can Kosukcu, Ekim Taskiran, Pelin Ozlem Simsek, Gulen Eda Utine, Koray Boduroglu, Ayfer Alikasifoglu, Mehmet Alikasifoglu
A rare cause of hyperinsulinemic hypoglycemia: Costello syndrome
Dogus Vuralli, Can Kosukcu, Ekim Taskiran, Pelin Ozlem Simsek, Gulen Eda Utine, Koray Boduroglu, Ayfer Alikasifoglu, Mehmet Alikasifoglu
P2-P194
Molecular defects identified by whole exome sequencing in a Chinese boy with fructose-1,6-bisphosphatase deficiency
Zhuo Huang, Jin Wu, Chengfa Xiang
Molecular defects identified by whole exome sequencing in a Chinese boy with fructose-1,6-bisphosphatase deficiency
Zhuo Huang, Jin Wu, Chengfa Xiang
P2-P195
The benefit of universal neonatal screening for hypoglycemia
Georges Nicolas, Riham chaaban, Marie-Claude faddous-Khalifeh, Juliana Souaiby, Yara Salemeh
The benefit of universal neonatal screening for hypoglycemia
Georges Nicolas, Riham chaaban, Marie-Claude faddous-Khalifeh, Juliana Souaiby, Yara Salemeh
P2-P196
Prematurity of 23 or less weeks' gestation is a risk for transient late-onset hyperglycemia in neonates
Takeru Yamauchi, Manabu Sugie, Kei Takasawa, Masatoshi Imamura, Kenichi Kashimada
Prematurity of 23 or less weeks' gestation is a risk for transient late-onset hyperglycemia in neonates
Takeru Yamauchi, Manabu Sugie, Kei Takasawa, Masatoshi Imamura, Kenichi Kashimada
P2-P197
An unusual cause of neonatal hyperglycemia – case report
Ana Luísa Leite, Isabel Ayres Pereira, Joana Matos, Rosa Arménia Campos, Helena Santos
An unusual cause of neonatal hyperglycemia – case report
Ana Luísa Leite, Isabel Ayres Pereira, Joana Matos, Rosa Arménia Campos, Helena Santos
P2-P198
Neonatal Hypocalcemia due to Maternal Hypovitaminosis D: a cohort of children in a region of Northern Spain
MARIA LAURA BERTHOLT ZUBER, CONCEPCIÓN FREIJO MARTIN, PILAR GORTAZAR ARIAS, SONIA VILANOVA FERNANDEZ, ANA BELÉN PÉREZ SANTOS, MARIA GARMENDIA AMUNARRIZ, INMACULADA PALENZUELA REVUELTA
Neonatal Hypocalcemia due to Maternal Hypovitaminosis D: a cohort of children in a region of Northern Spain
MARIA LAURA BERTHOLT ZUBER, CONCEPCIÓN FREIJO MARTIN, PILAR GORTAZAR ARIAS, SONIA VILANOVA FERNANDEZ, ANA BELÉN PÉREZ SANTOS, MARIA GARMENDIA AMUNARRIZ, INMACULADA PALENZUELA REVUELTA
P2-P199
Evaluation of vitamin D status and its correlation with gonadal function in children at mini-puberty
Suna Kılınç, Enver Atay
Evaluation of vitamin D status and its correlation with gonadal function in children at mini-puberty
Suna Kılınç, Enver Atay
P2-P200
Systemic pseudohypoaldosteronism type 1 due to 3 novel mutations in SCNN1A and SCNN1B genes; report of 3 cases
Atilla Cayir, Yasar Demirelli, Duran Yildiz, Hasan Kahveci, Oguzhan Yarali, Dogus Vuralli Karaoglan, Erdal Kurnaz, Huseyin Demirbilek
Systemic pseudohypoaldosteronism type 1 due to 3 novel mutations in SCNN1A and SCNN1B genes; report of 3 cases
Atilla Cayir, Yasar Demirelli, Duran Yildiz, Hasan Kahveci, Oguzhan Yarali, Dogus Vuralli Karaoglan, Erdal Kurnaz, Huseyin Demirbilek
P2-P201
Postnatal growth of infants with Neonatal Diabetes: Insulin pump (CSII) versus Multiple Daily Injection (MDI) therapy
Fawzia Alyafie, Ashraf Soliman, Amal Sabt, Nagwa Eldarsy, Mona Elgamal
Postnatal growth of infants with Neonatal Diabetes: Insulin pump (CSII) versus Multiple Daily Injection (MDI) therapy
Fawzia Alyafie, Ashraf Soliman, Amal Sabt, Nagwa Eldarsy, Mona Elgamal
P2-P202
Serum vaspin concentration in full-term, appropriate-for-gestational-age newborns: effect of early-onset infections
Małgorzata Stojewska, Dominika Wiśniewska-Ulfik
Serum vaspin concentration in full-term, appropriate-for-gestational-age newborns: effect of early-onset infections
Małgorzata Stojewska, Dominika Wiśniewska-Ulfik
P2-P203
First Three Years of the Congenital Adrenal Hyperplasia Neonatal Screening Program of the State of Parana, Southern Brazil
GABRIELA KRAEMER, SUZANA NESI-FRANÇA, LUIZ DE LACERDA, MARCELLA LIMA, JULIENNE CARVALHO, MOUSELINE DOMINGOS, IVY FURTADO, ROSANA PEREIRA
First Three Years of the Congenital Adrenal Hyperplasia Neonatal Screening Program of the State of Parana, Southern Brazil
GABRIELA KRAEMER, SUZANA NESI-FRANÇA, LUIZ DE LACERDA, MARCELLA LIMA, JULIENNE CARVALHO, MOUSELINE DOMINGOS, IVY FURTADO, ROSANA PEREIRA
P2-P204
Assessment of the stretched penile length in Sri Lankan newborns
Dona Udeni Anuruddhika Kollurage, Navoda Atapattu, Deepal Jayamanna, Janaka Ravinath Gunasiri, Shamya De Silva
Assessment of the stretched penile length in Sri Lankan newborns
Dona Udeni Anuruddhika Kollurage, Navoda Atapattu, Deepal Jayamanna, Janaka Ravinath Gunasiri, Shamya De Silva
P2-P205
Auxological catch up growth and evaluation of spontaneous motility in the term newborn Small for Gestational Age employing the Prechtl assessment of General Movements.
Laura Lucaccioni, Giovanna Talucci, Francesco Leo, Silvia Ciancia, Giovanna Russo, Fabrizio Ferrari, Lorenzo Iughetti
Auxological catch up growth and evaluation of spontaneous motility in the term newborn Small for Gestational Age employing the Prechtl assessment of General Movements.
Laura Lucaccioni, Giovanna Talucci, Francesco Leo, Silvia Ciancia, Giovanna Russo, Fabrizio Ferrari, Lorenzo Iughetti
P3-P170
A rare case of congeintal hyperinsulinemina with ABCC8 missense mutation presenting with focal pancreatic lesion
Aashish Sethi, Smita Ramachandran, Inderpal Kochar
A rare case of congeintal hyperinsulinemina with ABCC8 missense mutation presenting with focal pancreatic lesion
Aashish Sethi, Smita Ramachandran, Inderpal Kochar
P3-P171
Comparison of metabolic parameters of children's blood depending on the level of mother's glycemia during pregnancy
Alisa Masel, Ekaterina Kaprior, Alexandra Polyanskaya, Irina Nikitina
Comparison of metabolic parameters of children's blood depending on the level of mother's glycemia during pregnancy
Alisa Masel, Ekaterina Kaprior, Alexandra Polyanskaya, Irina Nikitina
P3-P172
Forty patients with persistent, non-focal congenital hyperinsulinism: Urgent need for new treatment modalities
Amalie Greve Rasmussen, Maria Melikian, Evgenia Globa, Sönke Detlefsen, Lars Rasmussen, Henrik Petersen, Klaus Brusgaard, Annett Helleskov Rasmussen, Henrik Christesen
Forty patients with persistent, non-focal congenital hyperinsulinism: Urgent need for new treatment modalities
Amalie Greve Rasmussen, Maria Melikian, Evgenia Globa, Sönke Detlefsen, Lars Rasmussen, Henrik Petersen, Klaus Brusgaard, Annett Helleskov Rasmussen, Henrik Christesen
P3-P173
Outcome of eight patients with congenital hyperinsulinism (CHI) studied with 18[F]Dihydroxyphenyl-Alanine Positron Emission Tomography Imaging (18F-DOPA-PET-CT) in Argentina
ANA TANGARI SAREDO, Sarah Flanagan, Guillermo Alonso, Juan Caceres, Marina Troiano, Horacio Bignon, Maria Bastianello, Del Rey Graciela, Bergadá Ignacio
Outcome of eight patients with congenital hyperinsulinism (CHI) studied with 18[F]Dihydroxyphenyl-Alanine Positron Emission Tomography Imaging (18F-DOPA-PET-CT) in Argentina
ANA TANGARI SAREDO, Sarah Flanagan, Guillermo Alonso, Juan Caceres, Marina Troiano, Horacio Bignon, Maria Bastianello, Del Rey Graciela, Bergadá Ignacio
P3-P174
Congenital Hyperinsulinism and Maple Syrup Urine disease a challenging combination
Azza Al Shidhani, Fathiya Al Murshedi, Saif Al Yaarubi, Khalid Al Thihli, irfan Ullah
Congenital Hyperinsulinism and Maple Syrup Urine disease a challenging combination
Azza Al Shidhani, Fathiya Al Murshedi, Saif Al Yaarubi, Khalid Al Thihli, irfan Ullah
P3-P175
Neonatal Diabetes Mellitus in Vietnam National Children Hospital
Can Thi Bich Ngoc, Vu Chi Dung, Bui Phuong Thao, Nguyen Ngoc Khanh, Do Thi Thanh Mai, Sian Ellard, Houghton Jayne, Sarah Flanagan, Deborah Mackay, Nguyen Thi Hoan
Neonatal Diabetes Mellitus in Vietnam National Children Hospital
Can Thi Bich Ngoc, Vu Chi Dung, Bui Phuong Thao, Nguyen Ngoc Khanh, Do Thi Thanh Mai, Sian Ellard, Houghton Jayne, Sarah Flanagan, Deborah Mackay, Nguyen Thi Hoan
P3-P176
Axillary temperature relation to blood serum insulin-like Growth Factor-I in the not-life-threatened newborn: relevance of preterm birth
Cesare Terzi, Werner F. Blum, Cristiana Magnani, Gabriele Tridenti, Andrea Cerioli, Marco Riani, Lidia Garavelli, Sergio Bernasconi, Gian Luigi De Angelis, Raffaele Virdis, Giacomo Banchini
Axillary temperature relation to blood serum insulin-like Growth Factor-I in the not-life-threatened newborn: relevance of preterm birth
Cesare Terzi, Werner F. Blum, Cristiana Magnani, Gabriele Tridenti, Andrea Cerioli, Marco Riani, Lidia Garavelli, Sergio Bernasconi, Gian Luigi De Angelis, Raffaele Virdis, Giacomo Banchini
P3-P177
Birth estimated brain weight relation to ratios between insulin-like Growth Factor-II and insulin-like Growth Factor Binding Protein-3 in the not-life-threatened newborn: relevance
Cesare Terzi, Raffaele Virdis, Cristiana Magnani, Gabriele Tridenti, Andrea Cerioli, Marco Riani, Elena Chesi, Sergio Bernasconi, Gian Luigi De Angelis, Werner F. Blum, Giacomo Banchini
Birth estimated brain weight relation to ratios between insulin-like Growth Factor-II and insulin-like Growth Factor Binding Protein-3 in the not-life-threatened newborn: relevance
Cesare Terzi, Raffaele Virdis, Cristiana Magnani, Gabriele Tridenti, Andrea Cerioli, Marco Riani, Elena Chesi, Sergio Bernasconi, Gian Luigi De Angelis, Werner F. Blum, Giacomo Banchini
P3-P178
Congenital Hyperinsulinism in children with Beckwith-Wiedemann syndrome
Diliara Gubaeva, Maria Melikyan, Mohammed Didi, Senthil Senniappan
Congenital Hyperinsulinism in children with Beckwith-Wiedemann syndrome
Diliara Gubaeva, Maria Melikyan, Mohammed Didi, Senthil Senniappan
P3-P179
Comparison of the phenylketonuria phenotypes in Qazvin province before and after neonatal screening until 2017
Fatemeh Saffari, Camelia Taherkhani, Neda Esmailzadehha, Ali Homaei
Comparison of the phenylketonuria phenotypes in Qazvin province before and after neonatal screening until 2017
Fatemeh Saffari, Camelia Taherkhani, Neda Esmailzadehha, Ali Homaei
P3-P181
Population screening of hypophosphatasia. A metabolopathy to consider. National multicentric study
Koldo Aldámiz-Echevarria, Ignacio Diez-Lopez, Leonor Arranz, MJ Garcia-Barcina
Population screening of hypophosphatasia. A metabolopathy to consider. National multicentric study
Koldo Aldámiz-Echevarria, Ignacio Diez-Lopez, Leonor Arranz, MJ Garcia-Barcina
P3-P182
Dumping Syndrome in a neonate with Esophagical Atresia Surgery
Angelica Gonzalez, Carolina Jaramillo, Jennyfer Monroy Espejo
Dumping Syndrome in a neonate with Esophagical Atresia Surgery
Angelica Gonzalez, Carolina Jaramillo, Jennyfer Monroy Espejo
P3-P183
Diagnosis and treatment of persistent hyperkalemia in newborn twins - rare case report of Gordon syndrome
Jun Zhang, Huamei Ma, Yanhong Li, Song Guo, Minlian Du, Muxue Yu, Xiaoyu Li
Diagnosis and treatment of persistent hyperkalemia in newborn twins - rare case report of Gordon syndrome
Jun Zhang, Huamei Ma, Yanhong Li, Song Guo, Minlian Du, Muxue Yu, Xiaoyu Li
P3-P184
Mutation in UCP2 gene: a rare cause of Hyperinsulinemic Hypoglycaemia Syndrome in a small-for-gestational age newborn
Maria Clemente, Pamela Yesquen, Ariadna Campos, Eduard Mogas, Mónica Fernández, Diego Yeste
Mutation in UCP2 gene: a rare cause of Hyperinsulinemic Hypoglycaemia Syndrome in a small-for-gestational age newborn
Maria Clemente, Pamela Yesquen, Ariadna Campos, Eduard Mogas, Mónica Fernández, Diego Yeste
P3-P185
Hyperinsulinemic Hypoglycaemia Syndrome in small-for-gestational age newborns: clinical characteristics and genetic study
Pamela Yesquen, Maria Clemente, Ariadna Campos, Mónica Fernández, Felix Castillo, Diego Yeste
Hyperinsulinemic Hypoglycaemia Syndrome in small-for-gestational age newborns: clinical characteristics and genetic study
Pamela Yesquen, Maria Clemente, Ariadna Campos, Mónica Fernández, Felix Castillo, Diego Yeste
P3-P186
Pediatric insulinoma: A case report
Pathikan Dissaneevate, Sakda Patarapinyokul, Araya Khaimook
Pediatric insulinoma: A case report
Pathikan Dissaneevate, Sakda Patarapinyokul, Araya Khaimook
P3-P187
Mutations in Indian children with Neonatal diabetes
Smita Ramachandran, Aashish Sethi, Inderpal Kochar
Mutations in Indian children with Neonatal diabetes
Smita Ramachandran, Aashish Sethi, Inderpal Kochar
P3-P188
Weight outcome in infants with prolonged hyperinsulinemic hypoglycemia treated with Diazoxide versus those with spontaneous resolution
SURESH CHANDRAN, VICTOR SAMUEL RAJADURAI, CHNG HUI YI, LIN JINJIE, JOYCE LIM, FABIAN YAP KOK PENG
Weight outcome in infants with prolonged hyperinsulinemic hypoglycemia treated with Diazoxide versus those with spontaneous resolution
SURESH CHANDRAN, VICTOR SAMUEL RAJADURAI, CHNG HUI YI, LIN JINJIE, JOYCE LIM, FABIAN YAP KOK PENG
P3-P189
Neonatal hyper- and hypoglycaemia; widening the clinical phenotype of transient neonatal diabetes mellitus due to 6q24 methylation defects
Tashunka Taylor-Miller, Michele O'Connell, Matthew Sabin
Neonatal hyper- and hypoglycaemia; widening the clinical phenotype of transient neonatal diabetes mellitus due to 6q24 methylation defects
Tashunka Taylor-Miller, Michele O'Connell, Matthew Sabin
P3-P190
Clinical and molecular genetic characterization of two patients due to mutations
Yu Ding, Niu Li, Guoying Chang, Juan Li, Ruen Yao, Yiping Shen, Jian Wang, Xiaodong Huang, Xiumin Wang
Clinical and molecular genetic characterization of two patients due to mutations
Yu Ding, Niu Li, Guoying Chang, Juan Li, Ruen Yao, Yiping Shen, Jian Wang, Xiaodong Huang, Xiumin Wang
P3-P191
Transient Central Hypothyroidism due to Maternal Graves’ disease
Yukie Izumita, Yuki Abe, Shinya Tsukano
Transient Central Hypothyroidism due to Maternal Graves’ disease
Yukie Izumita, Yuki Abe, Shinya Tsukano
RFC7.1
Next generation sequencing results in 142 patients with congenital hyperinsulinism
Diliara Gubaeva, Maria Melikyan, Eugeny Vasiliev, Vasily Petrov, Anatoly Tiulpakov
Next generation sequencing results in 142 patients with congenital hyperinsulinism
Diliara Gubaeva, Maria Melikyan, Eugeny Vasiliev, Vasily Petrov, Anatoly Tiulpakov
RFC7.2
Outcomes of a quality improvement project integrating Continuous Glucose Monitoring Systems into the routine management of neonatal hypoglycaemia
Sinead McGlacken-Byrne, Allan Jenkinson, Roisin O'Neill, John Murphy
Outcomes of a quality improvement project integrating Continuous Glucose Monitoring Systems into the routine management of neonatal hypoglycaemia
Sinead McGlacken-Byrne, Allan Jenkinson, Roisin O'Neill, John Murphy
RFC7.3
Central venous cathether-associated thrombosis in children with congenital hyperinsulinism
Daphne Yau, Maria Salomon-Estebanez, Amish Chinoy, Philip G Murray, Indi Banerjee
Central venous cathether-associated thrombosis in children with congenital hyperinsulinism
Daphne Yau, Maria Salomon-Estebanez, Amish Chinoy, Philip G Murray, Indi Banerjee
RFC7.4
Expression of MIR-576-5p in umbilical cord as a novel biomarker for the identification of catch-up growth in small-for-gestational-age infants
Judit Bassols, Berta Mas-Pares, Alexandra Bonmati, Silvia Xargay-Torrent, Gemma Carreras-Badosa, Esther Lizarraga-Mollinedo, Jose-Maria Martinez-Calcerrada, Francis de Zegher, Lourdes Ibañez, Abel Lopez-Bermejo
Expression of MIR-576-5p in umbilical cord as a novel biomarker for the identification of catch-up growth in small-for-gestational-age infants
Judit Bassols, Berta Mas-Pares, Alexandra Bonmati, Silvia Xargay-Torrent, Gemma Carreras-Badosa, Esther Lizarraga-Mollinedo, Jose-Maria Martinez-Calcerrada, Francis de Zegher, Lourdes Ibañez, Abel Lopez-Bermejo
RFC7.5
Alteration of renal corticosteroid signaling pathways in preterm infants: neonatal adaptation and developmental programming of hypertension
Laurence Dumeige, Melanie Nehlich, Christophe Lhadj, Say Viengchareun, Qiong-Yao Xue, Eric Pussard, Marc Lombès, Laetitia Martinerie
Alteration of renal corticosteroid signaling pathways in preterm infants: neonatal adaptation and developmental programming of hypertension
Laurence Dumeige, Melanie Nehlich, Christophe Lhadj, Say Viengchareun, Qiong-Yao Xue, Eric Pussard, Marc Lombès, Laetitia Martinerie
RFC7.6
Assessment of Pituitary Stalk Anatomy by T2 DRIVE without Gadolinium in Pituitary Diseases
Flavia Napoli, Elisabetta Godano, Giovanni Morana, Natascia Di Iorgi, Angela Pistorio, Anna Elsa Maria Allegri, Roberto Gastaldi, Annalisa Calcagno, Giuseppa Patti, Annalisa Gallizia, Sara Notarnicola, Marta Giaccardi, Serena Noli, Mariasavina Severino, Domenico Tortora, Andrea Rossi, Mohamad Maghnie
Assessment of Pituitary Stalk Anatomy by T2 DRIVE without Gadolinium in Pituitary Diseases
Flavia Napoli, Elisabetta Godano, Giovanni Morana, Natascia Di Iorgi, Angela Pistorio, Anna Elsa Maria Allegri, Roberto Gastaldi, Annalisa Calcagno, Giuseppa Patti, Annalisa Gallizia, Sara Notarnicola, Marta Giaccardi, Serena Noli, Mariasavina Severino, Domenico Tortora, Andrea Rossi, Mohamad Maghnie
FC10.6
Primary ovarian insufficiency incidence rate and etiology among Israeli adolescents between the years 2000-2016 – A multi-center study
Noah Gruber, Shir Kugler, Liat de Vries, Avivit Brener, Amnon Zung, Ori Eyal, Marianna Rachmiel, Ilana Koren, Yardena Tenenbaum-Rakover, Eli Hershkovitz, Zohar Landau, Meirav Oren, Alon Eliakim, David Zangen, Alina German, Hussein Majdoub, Kineret Mazor-Aronovitch, Dalit Modan-Moses, Yonatan Yeshayahu, Larisa Naugolni, Yael Levy-Shraga, Michal Ben-Ami, Gherta Brill, Floris Levy-Khademi, Carmit Avnon-Ziv, Dov Tiosano, Shira Harel, Einat Kedem, Anat Segev-Becker, Yehuda Shoenfeld, Orit Pinhas-Hamiel
Primary ovarian insufficiency incidence rate and etiology among Israeli adolescents between the years 2000-2016 – A multi-center study
Noah Gruber, Shir Kugler, Liat de Vries, Avivit Brener, Amnon Zung, Ori Eyal, Marianna Rachmiel, Ilana Koren, Yardena Tenenbaum-Rakover, Eli Hershkovitz, Zohar Landau, Meirav Oren, Alon Eliakim, David Zangen, Alina German, Hussein Majdoub, Kineret Mazor-Aronovitch, Dalit Modan-Moses, Yonatan Yeshayahu, Larisa Naugolni, Yael Levy-Shraga, Michal Ben-Ami, Gherta Brill, Floris Levy-Khademi, Carmit Avnon-Ziv, Dov Tiosano, Shira Harel, Einat Kedem, Anat Segev-Becker, Yehuda Shoenfeld, Orit Pinhas-Hamiel
FC8.1
Estrogen Receptor 2 Variant as a novel cause for dysgenetic ovaries
Mariarosaria Lang-Muritano, Patrick Sproll, Sascha Wyss, Anne Kolly, Renate Hürlimann, Daniel Konrad, Anna Biason-Lauber
Estrogen Receptor 2 Variant as a novel cause for dysgenetic ovaries
Mariarosaria Lang-Muritano, Patrick Sproll, Sascha Wyss, Anne Kolly, Renate Hürlimann, Daniel Konrad, Anna Biason-Lauber
FC8.2
Partial restoration of biological effects of estrogen in a female with estrogen receptor α variant
Eva Feigerlova, Henrik Laurell, Herve Mittre, Marie-Laure Kottler, Marc Deshayes, Patrick Balaguer, William Bourget, Jean-François Arnal, Richard Maréchaud, Samy Hadjadj, Pierre Gourdy
Partial restoration of biological effects of estrogen in a female with estrogen receptor α variant
Eva Feigerlova, Henrik Laurell, Herve Mittre, Marie-Laure Kottler, Marc Deshayes, Patrick Balaguer, William Bourget, Jean-François Arnal, Richard Maréchaud, Samy Hadjadj, Pierre Gourdy
FC8.4
STARD8, a novel candidate gene for 46,XY disorders of sex development
Ivan Domènech Mercadé, Daniel Rodríguez Gutiérrez, Serge Nef, Anna Biason-Lauber
STARD8, a novel candidate gene for 46,XY disorders of sex development
Ivan Domènech Mercadé, Daniel Rodríguez Gutiérrez, Serge Nef, Anna Biason-Lauber
FC8.5
DEAH-box helicase 37defects (DXH37) deffects are a novel cause of 46,XY Gonadal Dysgenesis
Nathalia Gomes, Thatiana Silva, Antonio Lerario, Rafael Loch Batista, José Antonio Faria Junior, Daniela Moraes, Elaine Maria Frade Costa, Mirian Nishi, Luciani Renata Carvalho, María Verónica Forclaz, Regina Papazian, Alejandro Martinez-Aguayo, Leila Pedroso de Paula, Filomena Marino Carvalho, Erick Vilain, Hayk Barseghyan Barseghyan, Catherine Keegan, Sorahia Domenice, Berenice Bilharinho Mendonca
DEAH-box helicase 37defects (DXH37) deffects are a novel cause of 46,XY Gonadal Dysgenesis
Nathalia Gomes, Thatiana Silva, Antonio Lerario, Rafael Loch Batista, José Antonio Faria Junior, Daniela Moraes, Elaine Maria Frade Costa, Mirian Nishi, Luciani Renata Carvalho, María Verónica Forclaz, Regina Papazian, Alejandro Martinez-Aguayo, Leila Pedroso de Paula, Filomena Marino Carvalho, Erick Vilain, Hayk Barseghyan Barseghyan, Catherine Keegan, Sorahia Domenice, Berenice Bilharinho Mendonca
FC8.6
The roles of steroids in gonadal development and maintenance – insights from a zebrafish model of androgen and cortisol deficiency
James A. Oakes, Nan Li, Belinda Wistow, Karl-Heinz Storbeck, Vincent T. Cunliffe, Nils Krone
The roles of steroids in gonadal development and maintenance – insights from a zebrafish model of androgen and cortisol deficiency
James A. Oakes, Nan Li, Belinda Wistow, Karl-Heinz Storbeck, Vincent T. Cunliffe, Nils Krone
HA2
Generating a human gonadal cells model from terminal differentiated fibroblast-derived induced pluripotent stem cells
Daniel Rodríguez Gutiérrez, Wassim Eid, Anna Biason-Lauber
Generating a human gonadal cells model from terminal differentiated fibroblast-derived induced pluripotent stem cells
Daniel Rodríguez Gutiérrez, Wassim Eid, Anna Biason-Lauber
LB-P12
Disrupting the Norm: The experience of young people with DSD
Denise Steers, Georgia Andrews, Sunny Collings, Angela Ballantyne, Maria Stubbe, Esko Wiltshire
Disrupting the Norm: The experience of young people with DSD
Denise Steers, Georgia Andrews, Sunny Collings, Angela Ballantyne, Maria Stubbe, Esko Wiltshire
LB-P7
Mutational analysis of SRD5A2 and AR genes in Indian children with 46 XY disorders of sex development
Anil Kumar, Mohd Faruq, Ralf Werner, Rajni Sharma, Vandana Jain
Mutational analysis of SRD5A2 and AR genes in Indian children with 46 XY disorders of sex development
Anil Kumar, Mohd Faruq, Ralf Werner, Rajni Sharma, Vandana Jain
P1-P214
In silico and in vitro studies of human SRD5A2 variants in search for activating variants explaining androgen excess reveal additional loss of function variants
Efstathios Katharopoulos, Kay-Sara Sauter, Amit V. Pandey, Christa E. Flück
In silico and in vitro studies of human SRD5A2 variants in search for activating variants explaining androgen excess reveal additional loss of function variants
Efstathios Katharopoulos, Kay-Sara Sauter, Amit V. Pandey, Christa E. Flück
P1-P215
Mutations involving nuclear receptors and their cofactors as a major cause of 46,XX DSD
Anu Bashamboo, Caroline Eozenou, Denis Houzelstein, Joelle Bignon-Topalovic, John Achermann, Ken McElreavey
Mutations involving nuclear receptors and their cofactors as a major cause of 46,XX DSD
Anu Bashamboo, Caroline Eozenou, Denis Houzelstein, Joelle Bignon-Topalovic, John Achermann, Ken McElreavey
P1-P216
SDgeneMatch, a new tool to aid the identification of the genetic causes of DSD
Jeroen De Ridder, Anu Bashamboo, Elfride De Baere, Nils Krone, Rod Mitchell, Ewa Rajpert-De Meyts, Ed Tobias, Leendert Looijenga, John Achermann, Ralf Werner, Faisal Ahmed, Olaf Hiort, Andy Greenfiled, Ken McElreavey
SDgeneMatch, a new tool to aid the identification of the genetic causes of DSD
Jeroen De Ridder, Anu Bashamboo, Elfride De Baere, Nils Krone, Rod Mitchell, Ewa Rajpert-De Meyts, Ed Tobias, Leendert Looijenga, John Achermann, Ralf Werner, Faisal Ahmed, Olaf Hiort, Andy Greenfiled, Ken McElreavey
P1-P217
Reduced androgen receptor expression in patients with 45,X/46,XY mosaicism
Nadine Hornig, Jeta Demiri, Eva Murga, Almuth Caliebe, Hans-Udo Schweikert, Laura Audi, Ralf Werner, Olaf Hiort, Paul-Martin Holterhus
Reduced androgen receptor expression in patients with 45,X/46,XY mosaicism
Nadine Hornig, Jeta Demiri, Eva Murga, Almuth Caliebe, Hans-Udo Schweikert, Laura Audi, Ralf Werner, Olaf Hiort, Paul-Martin Holterhus
P1-P218
Primary gonadal dysgenesis in male 46,XY patients with NR5A1 variants predominantly affects Sertoli cell function
Julia Hoppmann, Ralf Werner, Ralf Lünstedt, Wiebke Birnbaum, Otfried Schwab, Louise Marshall, Lutz Wünsch, Olaf Hiort
Primary gonadal dysgenesis in male 46,XY patients with NR5A1 variants predominantly affects Sertoli cell function
Julia Hoppmann, Ralf Werner, Ralf Lünstedt, Wiebke Birnbaum, Otfried Schwab, Louise Marshall, Lutz Wünsch, Olaf Hiort
P1-P219
Evaluation of genetic etiology in patients with 46,XY disorders of sex development: one center experience
Agharza Aghayev, Guven Toksoy, Sukran Poyrazoglu, Birsen Karaman, Sahin Avci, Melek Yildiz, Zehra Yavas Abali, Umut Altunoglu, Firdevs Bas, Feyza Darendeliler, Seher Basaran, Oya Uyguner
Evaluation of genetic etiology in patients with 46,XY disorders of sex development: one center experience
Agharza Aghayev, Guven Toksoy, Sukran Poyrazoglu, Birsen Karaman, Sahin Avci, Melek Yildiz, Zehra Yavas Abali, Umut Altunoglu, Firdevs Bas, Feyza Darendeliler, Seher Basaran, Oya Uyguner
P1-P220
Pitfalls in the diagnosis of an infant with 46,XX DSD with Congenital Adrenal Hyperplasia due to Cytochrome P450 Oxidoreductase Deficiency - the value of simultaneous genetic analysis to the diagnosis in DSD
Jan Idkowiak, Zainaba Mohamed, Stephanie Allen, Harish Chandran, Liam McCarthy, Jeremy Kirk, Trevor Cole, Nils Krone
Pitfalls in the diagnosis of an infant with 46,XX DSD with Congenital Adrenal Hyperplasia due to Cytochrome P450 Oxidoreductase Deficiency - the value of simultaneous genetic analysis to the diagnosis in DSD
Jan Idkowiak, Zainaba Mohamed, Stephanie Allen, Harish Chandran, Liam McCarthy, Jeremy Kirk, Trevor Cole, Nils Krone
P1-P221
High Mobility Group Box 1 (HMGB1) and Insulin-Like Growth Factor Binding Protein-2 (IGFBP-2) are increased, insulin decreased and IL-6 unchanged in Follicular Fluid (FF) from Polycystic Ovarian Syndrome (PCOS)
Francesca Cirillo, Cecilia Catellani, Pietro Lazzeroni, Chiara Sartori, Daria Morini, Alessia Nicoli, Sergio Amarri, Giovanni Battista La Sala, Maria Elisabeth Street
High Mobility Group Box 1 (HMGB1) and Insulin-Like Growth Factor Binding Protein-2 (IGFBP-2) are increased, insulin decreased and IL-6 unchanged in Follicular Fluid (FF) from Polycystic Ovarian Syndrome (PCOS)
Francesca Cirillo, Cecilia Catellani, Pietro Lazzeroni, Chiara Sartori, Daria Morini, Alessia Nicoli, Sergio Amarri, Giovanni Battista La Sala, Maria Elisabeth Street
P1-P222
A de novo missense mutation in the 4th zinc finger of the WT1 gene causes 46,XY and 46,XX DSD in two sibs
Rita Bertalan MD PhD, Balázs Gellén MD PhD, Caroline Eozenou PhD, Kenneth McElreavey PhD, Anu Bashamboo PhD
A de novo missense mutation in the 4th zinc finger of the WT1 gene causes 46,XY and 46,XX DSD in two sibs
Rita Bertalan MD PhD, Balázs Gellén MD PhD, Caroline Eozenou PhD, Kenneth McElreavey PhD, Anu Bashamboo PhD
P1-P223
Sex-differences in reproductive hormones during mini-puberty in infants with normal and disordered sex development
Trine Holm Johannsen, Katharina M. Main, Marie Lindhardt Ljubicic, Tina Kold Jensen, Helle Raun Andersen, Marianne Skovsager Andersen, Jørgen Holm Petersen, Anna-Maria Andersson, Anders Juul
Sex-differences in reproductive hormones during mini-puberty in infants with normal and disordered sex development
Trine Holm Johannsen, Katharina M. Main, Marie Lindhardt Ljubicic, Tina Kold Jensen, Helle Raun Andersen, Marianne Skovsager Andersen, Jørgen Holm Petersen, Anna-Maria Andersson, Anders Juul
P1-P224
The “ExternalGenitaliaScore” to describe external genitalia in male and female infants. A Europeanmulticenter validation study
Saskia van der Straaten, Alexander Springer, Doris Hebenstreit, Aleksandra Zezic, Ursula Tonnhofer, Aneta Gawlik, Malgorzata Baumert, Kamila Szeliga, Sara Debulpaep, An Desloovere, Lloyd Tack, Koen Smets, Malgorzata Wasniewska, Domenico Corica, Mariarosa Calafiore Calafiore, Marie Lindhardt Ljubicic, Alexander Siegfried Busch, Anders Juul, Anna Nordenström, Jon Sigurdsson, Christa E. Flück, Tanja Haamberg, Stefanie Graf, Sabine E Hannema, Katja P. Wolffenbuttel, S. Faisal Ahmed, Martine Cools
The “ExternalGenitaliaScore” to describe external genitalia in male and female infants. A Europeanmulticenter validation study
Saskia van der Straaten, Alexander Springer, Doris Hebenstreit, Aleksandra Zezic, Ursula Tonnhofer, Aneta Gawlik, Malgorzata Baumert, Kamila Szeliga, Sara Debulpaep, An Desloovere, Lloyd Tack, Koen Smets, Malgorzata Wasniewska, Domenico Corica, Mariarosa Calafiore Calafiore, Marie Lindhardt Ljubicic, Alexander Siegfried Busch, Anders Juul, Anna Nordenström, Jon Sigurdsson, Christa E. Flück, Tanja Haamberg, Stefanie Graf, Sabine E Hannema, Katja P. Wolffenbuttel, S. Faisal Ahmed, Martine Cools
P1-P225
Living with clitoromegaly: aqualitative interview study of parent’s responses to clitoromegaly in Congenital Adrenal Hyperplasia (CAH) with or without appearance altering surgery
Julie Alderson, Nicky Nicoll, Maia Thornton, Julie Jones, Mars Skae, Elizabeth Crowne
Living with clitoromegaly: aqualitative interview study of parent’s responses to clitoromegaly in Congenital Adrenal Hyperplasia (CAH) with or without appearance altering surgery
Julie Alderson, Nicky Nicoll, Maia Thornton, Julie Jones, Mars Skae, Elizabeth Crowne
P1-P226
“You can put ideas into their heads”: parental concerns about children’s participation in DSD research
Julie Alderson, Nicky Nicoll, Maia Thornton, Julie Jones, Mars Skae, Elizabeth Crowne
“You can put ideas into their heads”: parental concerns about children’s participation in DSD research
Julie Alderson, Nicky Nicoll, Maia Thornton, Julie Jones, Mars Skae, Elizabeth Crowne
P1-P227
Testosterone levels in newborn boys and girls related to penile length, Anogenital distance (AGD) and External Genitalia Score (EGS)
Jon Sigurdsson, Inga Bartuseviciene, Anna Nordenström
Testosterone levels in newborn boys and girls related to penile length, Anogenital distance (AGD) and External Genitalia Score (EGS)
Jon Sigurdsson, Inga Bartuseviciene, Anna Nordenström
P1-P228
Clinical factors that determine surgical outcome following hypospadias repair
Fahad Aljuraibah, Angela Lucas-Herald, Rachael Nixon, Martyn Flett, Boma Lee, Mairi Steven, Stuart O'Toole, Faisal Ahmed
Clinical factors that determine surgical outcome following hypospadias repair
Fahad Aljuraibah, Angela Lucas-Herald, Rachael Nixon, Martyn Flett, Boma Lee, Mairi Steven, Stuart O'Toole, Faisal Ahmed
P1-P229
Prevalence of hypogonadism in prepubertal boys with cryptrochdism.
Romina P. Grinspon, Patricia Bedecarras, Silvia Gottlieb, Rodolfo A. Rey
Prevalence of hypogonadism in prepubertal boys with cryptrochdism.
Romina P. Grinspon, Patricia Bedecarras, Silvia Gottlieb, Rodolfo A. Rey
P1-P230
Testicular ultrasound measurements to stratify pituitary-gonadal hormone references in a cross-sectional Norwegian study of male puberty
Andre Madsen, Oehme Ninnie, Ingvild Bruserud, Mathieu Roelants, Geir Egil Eide, Jørn Sagen, Gunnar Mellgren, Pétur Júlíusson
Testicular ultrasound measurements to stratify pituitary-gonadal hormone references in a cross-sectional Norwegian study of male puberty
Andre Madsen, Oehme Ninnie, Ingvild Bruserud, Mathieu Roelants, Geir Egil Eide, Jørn Sagen, Gunnar Mellgren, Pétur Júlíusson
P1-P231
Altered vascular function in boys with hypospadias- role of reactive oxygen species
Angela K Lucas-Herald, Rheure Alves-Lopes, Laura Haddow, Stuart O'Toole, S Basith Amjad, Martyn Flett, Mairi Steven, Boma Lee, Augusto C Montezano, Syed Faisal Ahmed, Rhian M Touyz
Altered vascular function in boys with hypospadias- role of reactive oxygen species
Angela K Lucas-Herald, Rheure Alves-Lopes, Laura Haddow, Stuart O'Toole, S Basith Amjad, Martyn Flett, Mairi Steven, Boma Lee, Augusto C Montezano, Syed Faisal Ahmed, Rhian M Touyz
P1-P232
Gonadectomy for Adults With DSD Conditions In The International Disorders of Sex Development Registry
Angela K Lucas-Herald, Andreas Kyriakou, Jillian Bryce, Martina Rodie, Carlo Acerini, Wiebke Arlt, Antonio Balsamo, Federico Baronico, Silvano Bertelloni, Antonia Brooke, Hedi Claahsen van der Grinten, Martine Cools, Feyza Darendeliler, Justin H Davies, An Desloovere, Mona Ellaithi, Simona Fica, Aneta Gawlik, Tulay Guran, Sabine Hannema, Olaf Hiort, Paul-Martin Holterhus, Violeta Iotova, Farida Jennane, Katherine Lachlan, Dejun Li, Lidka Lisa, Inas Mazen, Wilchelm Mladenov, Klaus Mohnike, Lavinia Nedelea, Marek Niedziela, Anna Nordenstrom, Sukran Poyrazoglu, Rodolfo Rey, Rieko Tadokoro-Cuccaro, Naomi Weintrob, Syed Faisal Ahmed
Gonadectomy for Adults With DSD Conditions In The International Disorders of Sex Development Registry
Angela K Lucas-Herald, Andreas Kyriakou, Jillian Bryce, Martina Rodie, Carlo Acerini, Wiebke Arlt, Antonio Balsamo, Federico Baronico, Silvano Bertelloni, Antonia Brooke, Hedi Claahsen van der Grinten, Martine Cools, Feyza Darendeliler, Justin H Davies, An Desloovere, Mona Ellaithi, Simona Fica, Aneta Gawlik, Tulay Guran, Sabine Hannema, Olaf Hiort, Paul-Martin Holterhus, Violeta Iotova, Farida Jennane, Katherine Lachlan, Dejun Li, Lidka Lisa, Inas Mazen, Wilchelm Mladenov, Klaus Mohnike, Lavinia Nedelea, Marek Niedziela, Anna Nordenstrom, Sukran Poyrazoglu, Rodolfo Rey, Rieko Tadokoro-Cuccaro, Naomi Weintrob, Syed Faisal Ahmed
P1-P233
Phenotypic and genetic assessment of boys witha suspected XY disorder of sex development
Malika Alimussina, Louise A. Diver, Jane D. McNeilly, Angela K. Lucas-Herald, Edward S. Tobias, Ruth McGowan, Syed Faisal Ahmed
Phenotypic and genetic assessment of boys witha suspected XY disorder of sex development
Malika Alimussina, Louise A. Diver, Jane D. McNeilly, Angela K. Lucas-Herald, Edward S. Tobias, Ruth McGowan, Syed Faisal Ahmed
P1-P234
Pediatricians' attitudes and beliefs towards transgender persons
Nitsan Landau, Uri Hamiel, Itay Tokatly Latzer, Elinor Mauda, Noa Levek, Liana Tripto-Shkolnik, Orit Pinhas-Hamiel
Pediatricians' attitudes and beliefs towards transgender persons
Nitsan Landau, Uri Hamiel, Itay Tokatly Latzer, Elinor Mauda, Noa Levek, Liana Tripto-Shkolnik, Orit Pinhas-Hamiel
P1-P235
Diagnosis of adolescent Polycystic Ovary Syndrome (PCOS) according to the 2018 International Evidence-Based Guideline for the Assessment and Management of PCOS
Alexia Peña, Kathy Hoeger, Sharon Oberfield, Selma Wiitchel, Maria Vogiatzi, Marie Misso, Helena Teede
Diagnosis of adolescent Polycystic Ovary Syndrome (PCOS) according to the 2018 International Evidence-Based Guideline for the Assessment and Management of PCOS
Alexia Peña, Kathy Hoeger, Sharon Oberfield, Selma Wiitchel, Maria Vogiatzi, Marie Misso, Helena Teede
P1-P236
Identification and analysis of the genetic causes of premature ovarian failure (POF) in a cohort of adolescent girls
Marianna Rita Stancampiano, Silvia Laura Carla Meroni, Alessandra Di Lascio, Moira Gianninoto, Gianni Russo
Identification and analysis of the genetic causes of premature ovarian failure (POF) in a cohort of adolescent girls
Marianna Rita Stancampiano, Silvia Laura Carla Meroni, Alessandra Di Lascio, Moira Gianninoto, Gianni Russo
P1-P237
Premature ovarian insufficiency in girls caused by autosomal microdeletions: 3 case reports
Ke Yuan, Minfei He, Yanlan Fang, Jianfang Zhu, Li Liang, Chunlin Wang
Premature ovarian insufficiency in girls caused by autosomal microdeletions: 3 case reports
Ke Yuan, Minfei He, Yanlan Fang, Jianfang Zhu, Li Liang, Chunlin Wang
P1-P238
Effect of intrauterine growth restriction on ovarian follicle pool.
Valentina Pampanini, Daniela Germani, Antonella Puglianiello, Kirsi Jahnukainen, Lena Sahlin, Stefano Cianfarani, Olle Söder
Effect of intrauterine growth restriction on ovarian follicle pool.
Valentina Pampanini, Daniela Germani, Antonella Puglianiello, Kirsi Jahnukainen, Lena Sahlin, Stefano Cianfarani, Olle Söder
P1-P239
Sustainability of estradiol drug concentrations in cut matrix patches; a study of different brands with potential use for pubertal induction
Carina Ankarberg-Lindgren, Aneta Gawlik, Berit Kriström, Laura Mazzanti, Theo CJ Sas
Sustainability of estradiol drug concentrations in cut matrix patches; a study of different brands with potential use for pubertal induction
Carina Ankarberg-Lindgren, Aneta Gawlik, Berit Kriström, Laura Mazzanti, Theo CJ Sas
P1-P240
Serum Anti-Mullerian Hormone (AMH) concentrations and reduced Appendix Testis Estrogen Receptor expression in Cryptorchidism
Antonios Panagidis, Helen Kourea, Xenophon Sinopidis, Eirini Kostopoulou, Andrea Paola Rojas-Gil, Spyridon Skiadopoulos, George Georgiou, Bessie E. Spiliotis
Serum Anti-Mullerian Hormone (AMH) concentrations and reduced Appendix Testis Estrogen Receptor expression in Cryptorchidism
Antonios Panagidis, Helen Kourea, Xenophon Sinopidis, Eirini Kostopoulou, Andrea Paola Rojas-Gil, Spyridon Skiadopoulos, George Georgiou, Bessie E. Spiliotis
P1-P241
The comparisons of the adult height gain and the menarchal age of the girls with Central Precocious Puberty after Gonadotropin Releasing Hormone agonist alone and those treated with combined Growth Hormone therapy
SE YOUNG KIM, MINSUB KIM
The comparisons of the adult height gain and the menarchal age of the girls with Central Precocious Puberty after Gonadotropin Releasing Hormone agonist alone and those treated with combined Growth Hormone therapy
SE YOUNG KIM, MINSUB KIM
P1-P242
AMH level of infants with premature thelarche and possible relationship between AMH and mini-puberty
nursel muratoglu sahin, elvan bayramoglu, hatice nursun ozcan, erdal kurnaz, meliksah keskin, senay savas erdeve, semra cetinkaya, zehra aycan
AMH level of infants with premature thelarche and possible relationship between AMH and mini-puberty
nursel muratoglu sahin, elvan bayramoglu, hatice nursun ozcan, erdal kurnaz, meliksah keskin, senay savas erdeve, semra cetinkaya, zehra aycan
P1-P243
Circulating makorin ring finger protein 3 levels predict central precocious puberty in girls
Hwal Rim Jeong, Hye Jin Lee, Yeong Suk Shim, Min Jae Kang, Seung Yang, Il Tae Hwang
Circulating makorin ring finger protein 3 levels predict central precocious puberty in girls
Hwal Rim Jeong, Hye Jin Lee, Yeong Suk Shim, Min Jae Kang, Seung Yang, Il Tae Hwang
P1-P244
Polycystic Ovarian Syndrome in adolescents: characterising the clinical phenotype and the role of precision medicine
Harriet Gunn, Vathsala Agarwalla, Rachel Skinner, Bronwyn Milne, Kevin Mills, Katharine Steinbeck
Polycystic Ovarian Syndrome in adolescents: characterising the clinical phenotype and the role of precision medicine
Harriet Gunn, Vathsala Agarwalla, Rachel Skinner, Bronwyn Milne, Kevin Mills, Katharine Steinbeck
P1-P245
Thyroid function in central precocious puberty girls
Young-Jun Rhie, Hyo-Kyoung Nam, Kee-Hyoung Lee
Thyroid function in central precocious puberty girls
Young-Jun Rhie, Hyo-Kyoung Nam, Kee-Hyoung Lee
P1-P246
Clinical phenotypes and mutation spectrum of patients with isolated gonadotropin-releasing hormone deficiency in a single academic center
Han-Wook Yoo, Go Hun Seo, Arum Oh, Gu-Hwan Kim, Jin-Ho Choi
Clinical phenotypes and mutation spectrum of patients with isolated gonadotropin-releasing hormone deficiency in a single academic center
Han-Wook Yoo, Go Hun Seo, Arum Oh, Gu-Hwan Kim, Jin-Ho Choi
P1-P247
Evaluation of hormonal profiles and autoantibodies against sperm and Leydig cells in patients after testicular torsion treatment
Pawel Osemlak, Konrad Miszczuk, Grzegorz Jedrzejewski, Iwona Ben-Skowronek
Evaluation of hormonal profiles and autoantibodies against sperm and Leydig cells in patients after testicular torsion treatment
Pawel Osemlak, Konrad Miszczuk, Grzegorz Jedrzejewski, Iwona Ben-Skowronek
P2-P338
Physical assessment in Chinese children with 5a-reductase type 2 deficiency
Xiu Zhao, Yanning Song, Shaoke Chen, Xiumin Wang, Feihong Luo, Yu Yang, Linqi Chen, Ruimin Chen, Hui Chen, Zhe Su, Di Wu, Chunxiu Gong
Physical assessment in Chinese children with 5a-reductase type 2 deficiency
Xiu Zhao, Yanning Song, Shaoke Chen, Xiumin Wang, Feihong Luo, Yu Yang, Linqi Chen, Ruimin Chen, Hui Chen, Zhe Su, Di Wu, Chunxiu Gong
P2-P339
Results of exome sequencing in disorders of sex development
Marlies Kempers, Hedi Claahsen, Janielle van Alfen - van der Velden, Tuula Rinne
Results of exome sequencing in disorders of sex development
Marlies Kempers, Hedi Claahsen, Janielle van Alfen - van der Velden, Tuula Rinne
P2-P340
Awareness is the key: heavy delay in diagnosis of 17-β-Hydroxysteroid-Dehydrogenase III deficiency (17bHSD3D) and other insights and conclusions from a cohort of ten 17bHSD3D patients in Germany
Jakob Meinel, Nadine Grossmüller, Annette Richter-Unruh
Awareness is the key: heavy delay in diagnosis of 17-β-Hydroxysteroid-Dehydrogenase III deficiency (17bHSD3D) and other insights and conclusions from a cohort of ten 17bHSD3D patients in Germany
Jakob Meinel, Nadine Grossmüller, Annette Richter-Unruh
P2-P341
Evaluation of three patients with 46,XY Gonadal Dysgenesis due to Desert Hedgehog gene mutations
Sukran Poyrazoglu, Agharza Aghayev, Guven Toksoy, Birsen Karaman, Sahin Avci, Asli Derya Kardelen Al, Esin Karakilic Ozturan, Umut Altunoglu, Firdevs Bas, Seher Basaran, Oya Uyguner, Feyza Darendeliler
Evaluation of three patients with 46,XY Gonadal Dysgenesis due to Desert Hedgehog gene mutations
Sukran Poyrazoglu, Agharza Aghayev, Guven Toksoy, Birsen Karaman, Sahin Avci, Asli Derya Kardelen Al, Esin Karakilic Ozturan, Umut Altunoglu, Firdevs Bas, Seher Basaran, Oya Uyguner, Feyza Darendeliler
P2-P342
In-silico gene-protein analysis and clinical phenotype characterisation of three novel NR5A1/SF1 gene mutations presenting with 46,XY DSD
Rieko Tadokoro Cuccaro, Ajay Thankamony, A Emile J Hendriks, Sabah Alvi, Ruth Armstrong, Jonathan Bruty, Ieuan A Hughes, Carlo L Acerini
In-silico gene-protein analysis and clinical phenotype characterisation of three novel NR5A1/SF1 gene mutations presenting with 46,XY DSD
Rieko Tadokoro Cuccaro, Ajay Thankamony, A Emile J Hendriks, Sabah Alvi, Ruth Armstrong, Jonathan Bruty, Ieuan A Hughes, Carlo L Acerini
P2-P343
Clinical, biochemical, structural and functional characterization of a novel P450 oxidoreductase mutation causing virilization in a 46,XX patient
Núria Camats, Sara Benito-Sanz, Shaheena Parween, Juan-Pedro López-Siguero, Mónica Fernández-Cancio, Christa E Flück, Sameer S Udhane, Norio Kagawa, Laura Audí, Amit V Pandey
Clinical, biochemical, structural and functional characterization of a novel P450 oxidoreductase mutation causing virilization in a 46,XX patient
Núria Camats, Sara Benito-Sanz, Shaheena Parween, Juan-Pedro López-Siguero, Mónica Fernández-Cancio, Christa E Flück, Sameer S Udhane, Norio Kagawa, Laura Audí, Amit V Pandey
P2-P344
Copy-Number Variations of the human olfactory receptor gene family in patients with macromastia and prepubertal gynecomastia
Firdevs Baş, Birsen Karaman, Aslı Derya Kardelen Al, Somayyeh Heidargholizadeh, Adam Najaflı, Güven Toksoy, Şükran Poyrazoğlu, Melek Yıldız, Oya Uyguner, Seher Başaran, Feyza Darendeliler
Copy-Number Variations of the human olfactory receptor gene family in patients with macromastia and prepubertal gynecomastia
Firdevs Baş, Birsen Karaman, Aslı Derya Kardelen Al, Somayyeh Heidargholizadeh, Adam Najaflı, Güven Toksoy, Şükran Poyrazoğlu, Melek Yıldız, Oya Uyguner, Seher Başaran, Feyza Darendeliler
P2-P345
Histopathologic characterization of patients with 46,XX testicular and ovotesticular disorders of sex development.
María Sol Touzon, María Laura Galluzzo Mutti, Pablo Ramirez, Natalia Perez Garrido, Roxana Marino, Marcela Bailez, Mariana Costanzo, Gabriela Guercio, Elisa Vaiani, Marta Ciaccio, Marco Aurelio Rivarola, Alicia Belgorosky, Esperanza Berensztein
Histopathologic characterization of patients with 46,XX testicular and ovotesticular disorders of sex development.
María Sol Touzon, María Laura Galluzzo Mutti, Pablo Ramirez, Natalia Perez Garrido, Roxana Marino, Marcela Bailez, Mariana Costanzo, Gabriela Guercio, Elisa Vaiani, Marta Ciaccio, Marco Aurelio Rivarola, Alicia Belgorosky, Esperanza Berensztein
P2-P346
Current medical care of children and adolescents with disorders/differences of sex development in Switzerland
Grit Sommer, Daniel Konrad, Beatrice Kuhlmann, Dagmar l'Allemand, Franziska Phan-Hug, Michael Hauschild, Valerie Schwitzgebel, Paolo Tonella, Melanie Hess, Urs Zumsteg, Anna Lauber-Biason, Christa E. Flueck
Current medical care of children and adolescents with disorders/differences of sex development in Switzerland
Grit Sommer, Daniel Konrad, Beatrice Kuhlmann, Dagmar l'Allemand, Franziska Phan-Hug, Michael Hauschild, Valerie Schwitzgebel, Paolo Tonella, Melanie Hess, Urs Zumsteg, Anna Lauber-Biason, Christa E. Flueck
P2-P347
Clinical, laboratory and molecular genetic findings of patients with 17ß-Hydroxysteroid Dehydrogenase3 Deficiency
Sukran Poyrazoglu, Guven Toksoy, Agharza Aghayev, Birsen Karaman, Sahin Avci, Umut Altunoglu, Asli Derya Kardelen Al, Esin Karakilic Ozturan, Firdevs Bas, Seher Basaran, Oya Uyguner, Feyza Darendeliler
Clinical, laboratory and molecular genetic findings of patients with 17ß-Hydroxysteroid Dehydrogenase3 Deficiency
Sukran Poyrazoglu, Guven Toksoy, Agharza Aghayev, Birsen Karaman, Sahin Avci, Umut Altunoglu, Asli Derya Kardelen Al, Esin Karakilic Ozturan, Firdevs Bas, Seher Basaran, Oya Uyguner, Feyza Darendeliler
P2-P348
Revisiting the diagnosis: Next Generation Sequencing (NGS) identifies concurrence of PAIS ina previously reported case Of Klinefelter Syndrome (47,XXY) with hypospadias
Zainaba Mohamed, Stephanie Allen, Kirsten McKay Bounford, Jan Idkowiak, Caroline Godber, Harish Chandran, Liam McCarthy, Trevor Cole, Jeremy Kirk, Nils Krone
Revisiting the diagnosis: Next Generation Sequencing (NGS) identifies concurrence of PAIS ina previously reported case Of Klinefelter Syndrome (47,XXY) with hypospadias
Zainaba Mohamed, Stephanie Allen, Kirsten McKay Bounford, Jan Idkowiak, Caroline Godber, Harish Chandran, Liam McCarthy, Trevor Cole, Jeremy Kirk, Nils Krone
P2-P349
A 46,XX female with WT1 mutation, congenital nephrotic syndrome and a complex disorder of sex development
Sara Ciccone, Carla Bizzarri, Stefano Picca, Cinzia Orazi, Chiara Lucchetti, Marco Cappa
A 46,XX female with WT1 mutation, congenital nephrotic syndrome and a complex disorder of sex development
Sara Ciccone, Carla Bizzarri, Stefano Picca, Cinzia Orazi, Chiara Lucchetti, Marco Cappa
P2-P350
Psychological gender features and social abilities and in adolescent girls – influence of obesity and hyperandrogenism
Agnieszka Zachurzok, Agnieszka Pasztak-Opilka, Elzbieta Forys-Dworniczak, Agnieszka Drosdzol-Cop, Aneta Gawlik, Ewa Malecka-Tendera
Psychological gender features and social abilities and in adolescent girls – influence of obesity and hyperandrogenism
Agnieszka Zachurzok, Agnieszka Pasztak-Opilka, Elzbieta Forys-Dworniczak, Agnieszka Drosdzol-Cop, Aneta Gawlik, Ewa Malecka-Tendera
P2-P351
Two unrelated cases of severe insulin resistance due to insulin receptor mutation discovered during adolescence
AZGAL Maryam, BOUHOURS-NOUET Natacha, CAMARD Odile, ALLIX Ingrid, SUTEAU Valentine, BAILLEUL Justine, CAMPAS Marie-Neige, COUTANT Régis
Two unrelated cases of severe insulin resistance due to insulin receptor mutation discovered during adolescence
AZGAL Maryam, BOUHOURS-NOUET Natacha, CAMARD Odile, ALLIX Ingrid, SUTEAU Valentine, BAILLEUL Justine, CAMPAS Marie-Neige, COUTANT Régis
P2-P352
A systematic review of reported outcomes for hypospadias
Tina Lund Leunbach, Stuart O'Toole, Alexander Springer, Paula Williamson, S. Faisal Ahmed
A systematic review of reported outcomes for hypospadias
Tina Lund Leunbach, Stuart O'Toole, Alexander Springer, Paula Williamson, S. Faisal Ahmed
P2-P353
Young transgender people’s attitudes to fertility preservation and practice
Elena MONTI, Sandra WALTON-BETANCOURTH, Raheala WAFA, Alice ROBERTS, Sara KLECZEWSKI, Kirpal ADU-GYAMFI, Elaine PERKINS, Elizabeth WILLIAMSON, Gary BUTLER
Young transgender people’s attitudes to fertility preservation and practice
Elena MONTI, Sandra WALTON-BETANCOURTH, Raheala WAFA, Alice ROBERTS, Sara KLECZEWSKI, Kirpal ADU-GYAMFI, Elaine PERKINS, Elizabeth WILLIAMSON, Gary BUTLER
P2-P354
Etiology of disorders of sex development in Kenyan children and adolescents
Prisca Amolo, Paul laigong, Anjumanara Omar, Stenvert Drop
Etiology of disorders of sex development in Kenyan children and adolescents
Prisca Amolo, Paul laigong, Anjumanara Omar, Stenvert Drop
P2-P355
Adiponectin as a marker of peripheral insulin resistance in adolescents with polycystic ovarian syndrome (PCOS) and as a tool to suspect insulin receptor defects
Analía Freire, Mirta Gryngarten, María Gabriela Ballerini, Andrea Arcari, Sonia Viviana Bengolea, Paula Scaglia, Ignacio Bergadá, María Gabriela Ropelato
Adiponectin as a marker of peripheral insulin resistance in adolescents with polycystic ovarian syndrome (PCOS) and as a tool to suspect insulin receptor defects
Analía Freire, Mirta Gryngarten, María Gabriela Ballerini, Andrea Arcari, Sonia Viviana Bengolea, Paula Scaglia, Ignacio Bergadá, María Gabriela Ropelato
P2-P356
Diagnostic experiences and concerns in adolescents with polycystic ovary syndrome
Alexia Peña, Melanie Gibson-Helm, Stephanie Byrne, Sarah Cash, Louise Hull, Helena Teede
Diagnostic experiences and concerns in adolescents with polycystic ovary syndrome
Alexia Peña, Melanie Gibson-Helm, Stephanie Byrne, Sarah Cash, Louise Hull, Helena Teede
P2-P357
Impact of hydrocortisone treatment on clitoral size during first year of life in girls with Congenital Adrenal Hyperplasia (CAH)
Johan Svensson, Maria Halldin Stenlid, Agneta Nordenskjöld, Magdalena Fossum, Svetlana Lajic, Anna Nordentström
Impact of hydrocortisone treatment on clitoral size during first year of life in girls with Congenital Adrenal Hyperplasia (CAH)
Johan Svensson, Maria Halldin Stenlid, Agneta Nordenskjöld, Magdalena Fossum, Svetlana Lajic, Anna Nordentström
P2-P358
Persistent Mullerian duct syndrome: rare but important aetiology of an inguinal hernia and cryptorchidism in boys
Abdullah Bereket, Fuat Bugrul, Tarik Kirkgoz, Kivilcim Karadeniz Cerit, Arzu Canmemis, Serap Turan, Jean-Yves Picard, Halil Tugtepe, Tulay Guran
Persistent Mullerian duct syndrome: rare but important aetiology of an inguinal hernia and cryptorchidism in boys
Abdullah Bereket, Fuat Bugrul, Tarik Kirkgoz, Kivilcim Karadeniz Cerit, Arzu Canmemis, Serap Turan, Jean-Yves Picard, Halil Tugtepe, Tulay Guran
P2-P359
Clinical, hormonal and metabolic profile in adolescent girls treated with gonadotropin releasing hormone agonist for idiopathic central precocious puberty
Camelia Procopiuc, Cristina Dumitrescu, Madalina Vintila, Andra Caragheorgheopol, Andreea Brehar, Lidia Radomir, Iuliana Gherlan
Clinical, hormonal and metabolic profile in adolescent girls treated with gonadotropin releasing hormone agonist for idiopathic central precocious puberty
Camelia Procopiuc, Cristina Dumitrescu, Madalina Vintila, Andra Caragheorgheopol, Andreea Brehar, Lidia Radomir, Iuliana Gherlan
P2-P360
Spontaneous pregnancies in female survivors of childhood hematological malignancies post allogeneic haemopoietic stem cell transplantation
Samantha Lai-Ka Lee, Margaret Zacharin, Karin Tiedemann
Spontaneous pregnancies in female survivors of childhood hematological malignancies post allogeneic haemopoietic stem cell transplantation
Samantha Lai-Ka Lee, Margaret Zacharin, Karin Tiedemann
P2-P361
Towards an integrated approach to diagnosis of 46,XY disorder of sex development.
Zofia Kolesinska, James Jr Acierno, S. Faisal Ahmed, Karina Kapczuk, Anna Skorczyk-Werner, Hanna Mikos, Aleksandra Rojek, Maciej Krawczynski, Nelly Pitteloud, Marek Niedziela
Towards an integrated approach to diagnosis of 46,XY disorder of sex development.
Zofia Kolesinska, James Jr Acierno, S. Faisal Ahmed, Karina Kapczuk, Anna Skorczyk-Werner, Hanna Mikos, Aleksandra Rojek, Maciej Krawczynski, Nelly Pitteloud, Marek Niedziela
P2-P362
Mini-Puberty in Boys with Inguinal Cryptorchidism
Nadezda Raygorodskaya, Nina Bolotova, Kseniya Cherednikova, Nataliya Filina, Nataliya Nikolaeva
Mini-Puberty in Boys with Inguinal Cryptorchidism
Nadezda Raygorodskaya, Nina Bolotova, Kseniya Cherednikova, Nataliya Filina, Nataliya Nikolaeva
P2-P363
The human genital tubercle is steroidogenic organ at earlypregnancy
Iuliia Savchuk, Marie-Line Morvan, Jean Philippe Antignac, Kristina Gemzell-Danielsson, Bruno Le Bizec, Olle Söder, Konstantin Svechnikov
The human genital tubercle is steroidogenic organ at earlypregnancy
Iuliia Savchuk, Marie-Line Morvan, Jean Philippe Antignac, Kristina Gemzell-Danielsson, Bruno Le Bizec, Olle Söder, Konstantin Svechnikov
P2-P364
Transgender medicine is a significant part of paediatric endocrinology
Ralph Decker, Jens Jacobeit
Transgender medicine is a significant part of paediatric endocrinology
Ralph Decker, Jens Jacobeit
P2-P365
Prospective investigation of the the influence of triptorelin treatment on body weight and body mass index of girls who were diagnosed with idiopathic precocious puberty or early puberty
Seokjin Kang, Yejee Shim, Heung Sik Kim
Prospective investigation of the the influence of triptorelin treatment on body weight and body mass index of girls who were diagnosed with idiopathic precocious puberty or early puberty
Seokjin Kang, Yejee Shim, Heung Sik Kim
P2-P366
Genetic etiologies and gender outcomes of patients with disorders of sex development presenting with asymmetric gonads
Arum Oh, Yoon-Myung Kim, Go Hun Seo, Gu-Hwan Kim, Jin-Ho Choi, Han-Wook Yoo
Genetic etiologies and gender outcomes of patients with disorders of sex development presenting with asymmetric gonads
Arum Oh, Yoon-Myung Kim, Go Hun Seo, Gu-Hwan Kim, Jin-Ho Choi, Han-Wook Yoo
P2-P367
A rare form of ovotesticular DSD: diagnostic and management challenges
Kruthika Narayan, Julie Alderson, Nicky Nicoll, Guy Nicholls, Sarah Smithson, Elizabeth Crowne
A rare form of ovotesticular DSD: diagnostic and management challenges
Kruthika Narayan, Julie Alderson, Nicky Nicoll, Guy Nicholls, Sarah Smithson, Elizabeth Crowne
P2-P368
A case of gonadal dysgenesis due to a novel homozygous mutation in NR5A2 gene
Friederike Denzer, Christian Denzer, Nadine Hornig, Paul-Martin Holterhus, Olaf Hiort, Martin Wabitsch
A case of gonadal dysgenesis due to a novel homozygous mutation in NR5A2 gene
Friederike Denzer, Christian Denzer, Nadine Hornig, Paul-Martin Holterhus, Olaf Hiort, Martin Wabitsch
P2-P369
Assessment of initial investigation requested in adolescents with menstrual disorders
MARIA CHARAMANTA, LINA MICHALA, PETER DRAKAKIS, EPHIA YASMIN, SARAH CREIGHTON
Assessment of initial investigation requested in adolescents with menstrual disorders
MARIA CHARAMANTA, LINA MICHALA, PETER DRAKAKIS, EPHIA YASMIN, SARAH CREIGHTON
P2-P370
Persistent Müllerian Duct Syndrome in twin brothers caused by a novel mutation in the AMHR2 gene
Karolien Van De Maele, Marjan de Rademaeker, Inge Gies, Jesse Vanbesien, Daniel Klink, Veerle De Boe, Jean De Schepper
Persistent Müllerian Duct Syndrome in twin brothers caused by a novel mutation in the AMHR2 gene
Karolien Van De Maele, Marjan de Rademaeker, Inge Gies, Jesse Vanbesien, Daniel Klink, Veerle De Boe, Jean De Schepper
P2-P371
No difference in cognitive performance or gender role behaviour in men with and without hypospadias
Anna Strandqvist, Lisa Örtqvist, Louise Frisen, Agneta Nordenskjöld, Agneta Herlitz, Anna Nordenström
No difference in cognitive performance or gender role behaviour in men with and without hypospadias
Anna Strandqvist, Lisa Örtqvist, Louise Frisen, Agneta Nordenskjöld, Agneta Herlitz, Anna Nordenström
P2-P372
Assessment of the gonadotrophin–gonadal axis and Sertoli cell function in partial androgen insensitivity syndrome
Doaa khater, Magdy omar, Shaymaa Raafat
Assessment of the gonadotrophin–gonadal axis and Sertoli cell function in partial androgen insensitivity syndrome
Doaa khater, Magdy omar, Shaymaa Raafat
P2-P373
Prevalence and ethiologic factors of hirsutism in adolescents
Nılgun Kaplan, Zerrin Orbak, Hakan Doneray
Prevalence and ethiologic factors of hirsutism in adolescents
Nılgun Kaplan, Zerrin Orbak, Hakan Doneray
P2-P374
Evaluation of Serum Anti-Mullerian Hormone and Androstenedione levels in adolescents girls with menstrual irregularities
Betül Ersoy, Nurcan Hanedan, Candost Hanedan, Fatma Taneli
Evaluation of Serum Anti-Mullerian Hormone and Androstenedione levels in adolescents girls with menstrual irregularities
Betül Ersoy, Nurcan Hanedan, Candost Hanedan, Fatma Taneli
P2-P375
Could basal AMH replace hCG stimulation test in XY disorder of sex development cases
Shaymaa Raafat Elsayed, Magdy Omar Abdo, Haytham Elmetwaly Badawy, Hadeer Aly Abbassy, Duaa Khatter Yaseen
Could basal AMH replace hCG stimulation test in XY disorder of sex development cases
Shaymaa Raafat Elsayed, Magdy Omar Abdo, Haytham Elmetwaly Badawy, Hadeer Aly Abbassy, Duaa Khatter Yaseen
P3-P321
Gonadal tumor incidence in patients with disorders od sex development containing Y chromosome or Y-derived sequences - experience from one clinical center
Aneta Gawlik, Aleksandra Antosz, Agnieszka Drosdzol-Cop, Grzegorz Kudela, Tomasz Koszutski, Ewa Małecka - Tendera
Gonadal tumor incidence in patients with disorders od sex development containing Y chromosome or Y-derived sequences - experience from one clinical center
Aneta Gawlik, Aleksandra Antosz, Agnieszka Drosdzol-Cop, Grzegorz Kudela, Tomasz Koszutski, Ewa Małecka - Tendera
P3-P322
New method of surgical correction of female hypospadias in girls with disorders of sex development and stenosis of artificial introitus
Alexander Anikief, Dmitriy Brovin, Elena Volodko, Alexey Okulov
New method of surgical correction of female hypospadias in girls with disorders of sex development and stenosis of artificial introitus
Alexander Anikief, Dmitriy Brovin, Elena Volodko, Alexey Okulov
P3-P323
Novel Mutation in Two Related 46, XY Phenotypic Females with 17β-Hydroxysteroid Dehydrogenase 3 Deficiency
Alina German, Dov Tiosano, Boris Chertin, Sabea Nadeem, Yardena Tenenbaum-Rakover
Novel Mutation in Two Related 46, XY Phenotypic Females with 17β-Hydroxysteroid Dehydrogenase 3 Deficiency
Alina German, Dov Tiosano, Boris Chertin, Sabea Nadeem, Yardena Tenenbaum-Rakover
P3-P324
Challenges in managing 46, XY Partial gonadal dysgenesis in Saudi Arabia
Amir Babiker, Yassir Bin Afif, Mohammed Al Dubayee, Fahad Al Juraibah, Mohsen Al Atawi, Angham Al Mutair, Ibrahim Al Alwan
Challenges in managing 46, XY Partial gonadal dysgenesis in Saudi Arabia
Amir Babiker, Yassir Bin Afif, Mohammed Al Dubayee, Fahad Al Juraibah, Mohsen Al Atawi, Angham Al Mutair, Ibrahim Al Alwan
P3-P325
A paternally inheritedNR5A1mutation in a case of 46,XY partial gonadal dysgenesis
Andrea Maciel-Guerra, Helena Fabbri-Scallet, Gil Guerra-Junior, Maricilda De Mello
A paternally inheritedNR5A1mutation in a case of 46,XY partial gonadal dysgenesis
Andrea Maciel-Guerra, Helena Fabbri-Scallet, Gil Guerra-Junior, Maricilda De Mello
P3-P326
Clinical presentation and characteristics of DSD in Kenyan children and adolescents
Anjumanara Omar, Prisca Amolo, Paul laigong, Stenvert Drop
Clinical presentation and characteristics of DSD in Kenyan children and adolescents
Anjumanara Omar, Prisca Amolo, Paul laigong, Stenvert Drop
P3-P327
Evolutive profile of pauci-symptomatic forms of Mc Cune Albright syndrome
audrey cartault, emilie Tryoen, Françoise Paris, céline Bar, Catherine Pienkowski
Evolutive profile of pauci-symptomatic forms of Mc Cune Albright syndrome
audrey cartault, emilie Tryoen, Françoise Paris, céline Bar, Catherine Pienkowski
P3-P329
About a case of Leydig cell tumor associated with central precocious puberty
Bensalah Meryem, Aribi Yamina, Badrane Nour El Houda, Ouldkablia Samia
About a case of Leydig cell tumor associated with central precocious puberty
Bensalah Meryem, Aribi Yamina, Badrane Nour El Houda, Ouldkablia Samia
P3-P331
GnRH Analogues and Cross-Sex Hormonal therapy: side effects in Transgender Youth
Cristina Mora Palma, Julio Guerrero Fernández, Nerea Itza Martín, Arancha Ortiz Villalobos, Ana Coral Barreda Bonis, Luis Salamanca Fresno, Isabel González Casado
GnRH Analogues and Cross-Sex Hormonal therapy: side effects in Transgender Youth
Cristina Mora Palma, Julio Guerrero Fernández, Nerea Itza Martín, Arancha Ortiz Villalobos, Ana Coral Barreda Bonis, Luis Salamanca Fresno, Isabel González Casado
P3-P332
Klinefelter syndrome with low gonadotropin levels
Daria Berdyugina, Elena Bogova, Igor Chugunov, Anna Kolodkina, Tatyana Shyryaeva, Maria Kareva, Valentina Peterkova
Klinefelter syndrome with low gonadotropin levels
Daria Berdyugina, Elena Bogova, Igor Chugunov, Anna Kolodkina, Tatyana Shyryaeva, Maria Kareva, Valentina Peterkova
P3-P333
Young male adolescent with gender dysphoria (GD) / gender incongruence - a case presentation
Elpis-Athina Vlachopapadopoulou, Eirini Dikaiakou, Stavroula Karagianni, Stefanos Michalacos
Young male adolescent with gender dysphoria (GD) / gender incongruence - a case presentation
Elpis-Athina Vlachopapadopoulou, Eirini Dikaiakou, Stavroula Karagianni, Stefanos Michalacos
P3-P334
Effect of gonadotropin-releasing hormone agonist treatment in boys with central precocious puberty and early puberty
Eun Young Kim, Kyung Hee Yi, Jae Hee Lee
Effect of gonadotropin-releasing hormone agonist treatment in boys with central precocious puberty and early puberty
Eun Young Kim, Kyung Hee Yi, Jae Hee Lee
P3-P335
DSD in Ukraine: our experience
Yuliya Shcherbak, Nataliya Zelinska, Evgeniya Globa, Iryna Schevchenko, Anu Bashamboo, Kenneth MсElreavey
DSD in Ukraine: our experience
Yuliya Shcherbak, Nataliya Zelinska, Evgeniya Globa, Iryna Schevchenko, Anu Bashamboo, Kenneth MсElreavey
P3-P336
A Turkish family with 46,XY disorder of sex development due to 17b-hydroxysteroid dehydrogenase type 3 deficiency
fatih gurbuz, ihsan turan, mehmet tastan, bilgin yuksel
A Turkish family with 46,XY disorder of sex development due to 17b-hydroxysteroid dehydrogenase type 3 deficiency
fatih gurbuz, ihsan turan, mehmet tastan, bilgin yuksel
P3-P337
Normal External Genitalia in a Female with Classic, Salt-Wasting 21-hydroxylase deficiency
Hadeel Alsarraj
Normal External Genitalia in a Female with Classic, Salt-Wasting 21-hydroxylase deficiency
Hadeel Alsarraj
P3-P338
OVARIAN LEYDIG CELL TUMOR IN AN 8 YEARS OLD GIRL MISDIAGNOSED AS CONGENITAL ADRENAL HYPERPLASIA DUE TO ELEVATED 17-HYDROXI-PROGESTERONE
Mónica Arancibia, Hernán García-Fernández, Alejandro Martínez-Aguayo, Paulina Baquedano, Helena Poggi, Hernán García
OVARIAN LEYDIG CELL TUMOR IN AN 8 YEARS OLD GIRL MISDIAGNOSED AS CONGENITAL ADRENAL HYPERPLASIA DUE TO ELEVATED 17-HYDROXI-PROGESTERONE
Mónica Arancibia, Hernán García-Fernández, Alejandro Martínez-Aguayo, Paulina Baquedano, Helena Poggi, Hernán García
P3-P339
Analysis of genetic mutations in a Chinese pedigree affected with idiopathic hypogonadotropic hypogonadism Syndrome
Yu Yang, Hui Huang
Analysis of genetic mutations in a Chinese pedigree affected with idiopathic hypogonadotropic hypogonadism Syndrome
Yu Yang, Hui Huang
P3-P340
Cytogenetic spectrum of Ovotesticular Disorder of sex development in Egyptian DSD patients
inas Mazen, Mona Mekkawi, Nabil Dessouki
Cytogenetic spectrum of Ovotesticular Disorder of sex development in Egyptian DSD patients
inas Mazen, Mona Mekkawi, Nabil Dessouki
P3-P341
Cytogenetic spectrum of Ovotesticular Disorder of sex development in Egyptian DSD patients
Inas Mazen, Mona Mekkawi, Nabil Dessouki, Amal Mohammed, Alaa Kamel
Cytogenetic spectrum of Ovotesticular Disorder of sex development in Egyptian DSD patients
Inas Mazen, Mona Mekkawi, Nabil Dessouki, Amal Mohammed, Alaa Kamel
P3-P342
Characterization of Genotype-Phenotype in inter-familial and intra-familial patients with same mutation of SRD5A2 gene
IRAM SHABIR, RAJESH KHADGAWAT, RIMA DADA, VIVEKA P JYOTSNA
Characterization of Genotype-Phenotype in inter-familial and intra-familial patients with same mutation of SRD5A2 gene
IRAM SHABIR, RAJESH KHADGAWAT, RIMA DADA, VIVEKA P JYOTSNA
P3-P343
Genital abnormalities and management outcomes as seen in the University of Port Harcourt Teaching Hospital
Iroro Yarhere, Tamunopriye Jaja, Gift Clement-Wekere
Genital abnormalities and management outcomes as seen in the University of Port Harcourt Teaching Hospital
Iroro Yarhere, Tamunopriye Jaja, Gift Clement-Wekere
P3-P344
A case report: a girl with 46,XY karyotype and disorder of androgen synthesis
Jasna Šuput Omladič, Sara Bertok, Mojca Žerjav Tanšek, Jernej Kovač, Tadej Battelino, Michaela F Hartmann, Stefan A Wudy, Magdalena Avbelj Stefanija
A case report: a girl with 46,XY karyotype and disorder of androgen synthesis
Jasna Šuput Omladič, Sara Bertok, Mojca Žerjav Tanšek, Jernej Kovač, Tadej Battelino, Michaela F Hartmann, Stefan A Wudy, Magdalena Avbelj Stefanija
P3-P345
THE POSITIVE EFFECT OF THE LOW-DOSE CONTRACEPTIVE ON THE COURSE OF CYSTIC FIBROSIS IN THE ADOLESCENT FEMALE
Juliana Ferenczova, Anna Feketeová, Veronika Urbanová, Veronika Vargova
THE POSITIVE EFFECT OF THE LOW-DOSE CONTRACEPTIVE ON THE COURSE OF CYSTIC FIBROSIS IN THE ADOLESCENT FEMALE
Juliana Ferenczova, Anna Feketeová, Veronika Urbanová, Veronika Vargova
P3-P346
Ovotesticular disorder of sexual development: 31 cases followed-up in a single-center in Brazil
Julia Melardi, Diego Cunha, Marianna Ferreira, Nathalia Brigatti, Filomena Carvalho, Louise Cominato, Leandra Steinmetz, Durval Damiani
Ovotesticular disorder of sexual development: 31 cases followed-up in a single-center in Brazil
Julia Melardi, Diego Cunha, Marianna Ferreira, Nathalia Brigatti, Filomena Carvalho, Louise Cominato, Leandra Steinmetz, Durval Damiani
P3-P347
Genital swelling and ovarian stimulation syndrome in an extremely preterm infant
Maria Cristina Azcona, Amaia Ochotorena, Monica Prados, Jose Luis Leon, Valentin Alzina
Genital swelling and ovarian stimulation syndrome in an extremely preterm infant
Maria Cristina Azcona, Amaia Ochotorena, Monica Prados, Jose Luis Leon, Valentin Alzina
P3-P348
Significant penile growth with local DHT-gel in an infant with 17-beta HSD-deficiency
Maria Halldin Stenlid, Agneta Nordenskjöld, Louise Frisén, Johan Svensson, Svetlana Lajic, Anna Nordenström
Significant penile growth with local DHT-gel in an infant with 17-beta HSD-deficiency
Maria Halldin Stenlid, Agneta Nordenskjöld, Louise Frisén, Johan Svensson, Svetlana Lajic, Anna Nordenström
P3-P349
Mother and baby diagnosed Noonan syndrome with dysmorphic findings
Mehmet Keskin, Emel H.Aytac Kaplan, Murat Karaoglan, Kadri Karaer, Ozlem Keskin
Mother and baby diagnosed Noonan syndrome with dysmorphic findings
Mehmet Keskin, Emel H.Aytac Kaplan, Murat Karaoglan, Kadri Karaer, Ozlem Keskin
P3-P350
5-alpha reductase type 2 deficiency among Iranian patients with ambiguous genitalia
Bahareh Rabbani, Nejat Mahdieh, Ali Rabbani, Setila Dalili
5-alpha reductase type 2 deficiency among Iranian patients with ambiguous genitalia
Bahareh Rabbani, Nejat Mahdieh, Ali Rabbani, Setila Dalili
P3-P351
A case report of spironolactone treatment for Becker’s Nevus associated ipsilateral breast hypoplasia
Abhilasha Banerjee, Rosa Sherafat-Kazemzadeh
A case report of spironolactone treatment for Becker’s Nevus associated ipsilateral breast hypoplasia
Abhilasha Banerjee, Rosa Sherafat-Kazemzadeh
P3-P352
New mutation in 5-alpha-redoctase:a five-month-old infant with a karyotype of 46 xy
setila dalili, nejat mahdie
New mutation in 5-alpha-redoctase:a five-month-old infant with a karyotype of 46 xy
setila dalili, nejat mahdie
P3-P353
A novel compound heterozygous mutation in CYP19A1 resulting in aromatase deficiency with normal gonadotropin levels and ovarian tissue
Sezer Acar, Ahu Paketçi, Hüseyin Onay, Tufan Çankaya, Semra Gürsoy, Bayram Özhan, Ayhan Abacı, Erdener Özer, Mustafa Olguner, Ece Böber, Korcan Demir
A novel compound heterozygous mutation in CYP19A1 resulting in aromatase deficiency with normal gonadotropin levels and ovarian tissue
Sezer Acar, Ahu Paketçi, Hüseyin Onay, Tufan Çankaya, Semra Gürsoy, Bayram Özhan, Ayhan Abacı, Erdener Özer, Mustafa Olguner, Ece Böber, Korcan Demir
P3-P355
The Republic of Colombia has a constitutional jurisprudential precedent identified as T622 of 2014, this sentence reaffirms the importance of the accurate diagnosis of intersexual patients and updates how the state looks at them
Silvia Cristina Chahin Ferreyra, Federico Mejia Alvarez
The Republic of Colombia has a constitutional jurisprudential precedent identified as T622 of 2014, this sentence reaffirms the importance of the accurate diagnosis of intersexual patients and updates how the state looks at them
Silvia Cristina Chahin Ferreyra, Federico Mejia Alvarez
P3-P356
Paediatric doctors’ experience and knowledge of the initial management of neonatal ambiguous genitalia
Sinead McGlacken-Byrne, Kathryn Byrne, Mark O'Rahelly, Ethel Ryan
Paediatric doctors’ experience and knowledge of the initial management of neonatal ambiguous genitalia
Sinead McGlacken-Byrne, Kathryn Byrne, Mark O'Rahelly, Ethel Ryan
P3-P357
A case of Transverse Testicular Ectopia with Persistant Müllerian Duct Syndrome:a novel AMH gene mutation
Suna Kılınç, Tuğrul Çiçek, Serdar Moralıoğlu, Ayla Güven
A case of Transverse Testicular Ectopia with Persistant Müllerian Duct Syndrome:a novel AMH gene mutation
Suna Kılınç, Tuğrul Çiçek, Serdar Moralıoğlu, Ayla Güven
P3-P358
Argentinean first experience with transgender children and youths
Veronica Figueroa, Jimena Lopez Dacal, Carlos Sanz, Oscar Brunetto
Argentinean first experience with transgender children and youths
Veronica Figueroa, Jimena Lopez Dacal, Carlos Sanz, Oscar Brunetto
P3-P359
Long-term follow-up in a Chinese child with lipoid congenital adrenal hyperplasiadue to STARmutation
Xiu Zhao, Xia Liu, Li Wang, Lili Pan, Longjiang Zhang, Zhe SU
Long-term follow-up in a Chinese child with lipoid congenital adrenal hyperplasiadue to STARmutation
Xiu Zhao, Xia Liu, Li Wang, Lili Pan, Longjiang Zhang, Zhe SU
P3-P360
46, XY gonadal dysgenesis accompanied by neuropathy caused by a DHH mutation
Zhe Su, Lili Pan, Li Wang, Weiyan Chen, Jianming Song, Shoulin Li
46, XY gonadal dysgenesis accompanied by neuropathy caused by a DHH mutation
Zhe Su, Lili Pan, Li Wang, Weiyan Chen, Jianming Song, Shoulin Li
P3-P400
CLINICAL AND MOLECULAR CHARACTERIZATION OF ONE NR5A1 GENE MUTATION FOUND IN A PATIENT WITH 46, XY DSD
AMAYA VELA, IDOIA MARTINEZ DE LAPISCINA, GUSTAVO PEREZ DE NANCLARES, RODRIGUEZ AMAIA, ITXASO RICA, LUIS CASTAÑO, GEMA GRAU
CLINICAL AND MOLECULAR CHARACTERIZATION OF ONE NR5A1 GENE MUTATION FOUND IN A PATIENT WITH 46, XY DSD
AMAYA VELA, IDOIA MARTINEZ DE LAPISCINA, GUSTAVO PEREZ DE NANCLARES, RODRIGUEZ AMAIA, ITXASO RICA, LUIS CASTAÑO, GEMA GRAU
P3-P408
GENETIC TESTING BY SNP ARRAY ANALYSIS IN A GROUP OF ROMANIAN PATIENTS WITH DISORDERS OF SEXUAL DEVELOPMENT
Diana Miclea, Camelia Alkhzouz, Simona Bucerzan, Victoria Cret, Maria Puiu, Paula Grigorescu-Sido
GENETIC TESTING BY SNP ARRAY ANALYSIS IN A GROUP OF ROMANIAN PATIENTS WITH DISORDERS OF SEXUAL DEVELOPMENT
Diana Miclea, Camelia Alkhzouz, Simona Bucerzan, Victoria Cret, Maria Puiu, Paula Grigorescu-Sido
P3-P409
A novel gene mutation and atypical clinical phenotype of Kallmann syndrome
Terada Yumiko, Yusuke Fujisawa, Yuta Chiba, Kenichi Kinjo, Atsushi Tsukamura, Tomoe Yamaguchi, Keisuke Yoshii, Yasuhiro Naiki, Reiko Horikawa
A novel gene mutation and atypical clinical phenotype of Kallmann syndrome
Terada Yumiko, Yusuke Fujisawa, Yuta Chiba, Kenichi Kinjo, Atsushi Tsukamura, Tomoe Yamaguchi, Keisuke Yoshii, Yasuhiro Naiki, Reiko Horikawa
RFC10.2
Non-inferiority clinical trial on gonadotropinversus pulsatile gonadotropin-releasing hormone infusion therapy in male adolescent patient withcongenital hypogonadotropic hypogonadism
Ying Liu, Chunxiu Gong
Non-inferiority clinical trial on gonadotropinversus pulsatile gonadotropin-releasing hormone infusion therapy in male adolescent patient withcongenital hypogonadotropic hypogonadism
Ying Liu, Chunxiu Gong
RFC10.4
Comparative analysis between immunoassay and tandem mass spectrometry for androgens before and after human recombinant gonadotrophin in children with genital ambiguity and 46,XY karyotype
LETÍCIA OLIVEIRA, GIL GUERRA-JUNIOR, CARLOS LONGUI, GUILHERME GUARAGNA-FILHO, JOSÉ LUIZ COSTA, RAFAEL LANARO, DAVID SILVA, MARICILDA MELLO, ANDREA MACIEL-GUERRA, ANDRE MORCILLO
Comparative analysis between immunoassay and tandem mass spectrometry for androgens before and after human recombinant gonadotrophin in children with genital ambiguity and 46,XY karyotype
LETÍCIA OLIVEIRA, GIL GUERRA-JUNIOR, CARLOS LONGUI, GUILHERME GUARAGNA-FILHO, JOSÉ LUIZ COSTA, RAFAEL LANARO, DAVID SILVA, MARICILDA MELLO, ANDREA MACIEL-GUERRA, ANDRE MORCILLO
RFC8.1
Male fertility genes located in Y-chromosomal regions display differential mRNA profiles in response to GnRH treatment of cryptorchidism-dependent infertility
Faruk Hadziselimovic, Katharina Gegenschatz-Schmid, Gilvidas Verkauskas, Michael Stadler
Male fertility genes located in Y-chromosomal regions display differential mRNA profiles in response to GnRH treatment of cryptorchidism-dependent infertility
Faruk Hadziselimovic, Katharina Gegenschatz-Schmid, Gilvidas Verkauskas, Michael Stadler
RFC8.2
High Mobility Group Box 1 (HMGB1) is increased in adolescents with Polycystic Ovarian Syndrome (PCOS) and decreases after treatment with myo-inositol in combination with α-lipoic acid (MYO+ALA)
Francesca Cirillo, Cecilia Catellani, Gabriele Tridenti, Cristina Vezzani, Pietro Lazzeroni, Chiara Sartori, Anna Maria Fulghesu, Simona Losi, Letizia Coradazzi, Sergio Amarri, Maria Elisabeth Street
High Mobility Group Box 1 (HMGB1) is increased in adolescents with Polycystic Ovarian Syndrome (PCOS) and decreases after treatment with myo-inositol in combination with α-lipoic acid (MYO+ALA)
Francesca Cirillo, Cecilia Catellani, Gabriele Tridenti, Cristina Vezzani, Pietro Lazzeroni, Chiara Sartori, Anna Maria Fulghesu, Simona Losi, Letizia Coradazzi, Sergio Amarri, Maria Elisabeth Street
RFC8.3
Pharmacological treatment of adolescent Polycystic Ovary Syndrome (PCOS) according to the 2018 International Evidence-Based Guideline for the Assessment and Management of PCOS
Alexia Pena, Selma Witchel, Kathy Hoeger, Sharon Oberfield, Maria Vogiatzi, Marie Misso, Helena Teede
Pharmacological treatment of adolescent Polycystic Ovary Syndrome (PCOS) according to the 2018 International Evidence-Based Guideline for the Assessment and Management of PCOS
Alexia Pena, Selma Witchel, Kathy Hoeger, Sharon Oberfield, Maria Vogiatzi, Marie Misso, Helena Teede
RFC8.4
Establishing age, sex, and method related reference ranges for anogenital distance - a marker of in utero androgen action
Marie Lindhardt Ljubicic, Ajay Thankamony, Carlo Acerini, Tina Kold Jensen, Katharina M. Main, Jørgen Holm Petersen, Alexander S. Busch, Emmie Upners, Casper P. Hagen, Shanna H. Swan, Anders Juul
Establishing age, sex, and method related reference ranges for anogenital distance - a marker of in utero androgen action
Marie Lindhardt Ljubicic, Ajay Thankamony, Carlo Acerini, Tina Kold Jensen, Katharina M. Main, Jørgen Holm Petersen, Alexander S. Busch, Emmie Upners, Casper P. Hagen, Shanna H. Swan, Anders Juul
RFC8.5
Latest progress in tissue engineered urethral regeneration. From rabbit to dog, a step from human clinical trial for surgical treatment of VSD (Variation of Sex Development)
Kalitha Pinnagoda, Ganesh Vythilingam, Elif Vardar, Eva-Maria Ballet, CR Tambidorai, Peter Frey, Hans-Mattias Larsson
Latest progress in tissue engineered urethral regeneration. From rabbit to dog, a step from human clinical trial for surgical treatment of VSD (Variation of Sex Development)
Kalitha Pinnagoda, Ganesh Vythilingam, Elif Vardar, Eva-Maria Ballet, CR Tambidorai, Peter Frey, Hans-Mattias Larsson
RFC8.6
Metabolic profile of young adult transgender persons who started gender affirming treatment in their adolescence
Maartje Klaver, Renée de Mutsert, Chantal Wiepjes, Martin den Heijer, Joost Rotteveel, Daniel Klink
Metabolic profile of young adult transgender persons who started gender affirming treatment in their adolescence
Maartje Klaver, Renée de Mutsert, Chantal Wiepjes, Martin den Heijer, Joost Rotteveel, Daniel Klink
FC12.1
Continuous glucose monitoring profiles in healthy non-diabetic children and adolescents:a multicenter prospective study
Stephanie DuBose, Zoey Li, Roy Beck, William Tamborlane
Continuous glucose monitoring profiles in healthy non-diabetic children and adolescents:a multicenter prospective study
Stephanie DuBose, Zoey Li, Roy Beck, William Tamborlane
FC12.2
Apoptosis and oxidative stress markers during the Oral Glucose Tolerance Test (OGTT)
Andrea Paola Rojas Gil, Maria Efthymia Katsa, Nomikos Tzortzis, Anastasios Ioannidis, Eirini Kostopoulou, Bessie E. Spiliotis
Apoptosis and oxidative stress markers during the Oral Glucose Tolerance Test (OGTT)
Andrea Paola Rojas Gil, Maria Efthymia Katsa, Nomikos Tzortzis, Anastasios Ioannidis, Eirini Kostopoulou, Bessie E. Spiliotis
FC12.3
Impact of insulin sensitivity and β-cell function on the development of impaired glucose tolerance (IGT) in obese European children and adolescents
Christian Denzer, Josef Vogt, Katja Kohlsdorf, Julia von Schnurbein, Martin Wabitsch
Impact of insulin sensitivity and β-cell function on the development of impaired glucose tolerance (IGT) in obese European children and adolescents
Christian Denzer, Josef Vogt, Katja Kohlsdorf, Julia von Schnurbein, Martin Wabitsch
FC12.4
How does thiol/disulphide homeostasis change in children with Type 1 Diabetes Mellitus?
sevgi yasar durmus, nursel muratoglu sahin, ozcan erel, salim neselioglu, zehra aycan
How does thiol/disulphide homeostasis change in children with Type 1 Diabetes Mellitus?
sevgi yasar durmus, nursel muratoglu sahin, ozcan erel, salim neselioglu, zehra aycan
FC12.5
Effect of Homocysteine-Lowering Therapy on Diabetic Nephropathy in children and adolescents with Type 1 Diabetes
Nancy Elbarbary, Eman Abdel Rahman Ismail, Mamdouh Ahmed Zaki, Marwa Zaki Ibrahim, Manal El- Hamamsy
Effect of Homocysteine-Lowering Therapy on Diabetic Nephropathy in children and adolescents with Type 1 Diabetes
Nancy Elbarbary, Eman Abdel Rahman Ismail, Mamdouh Ahmed Zaki, Marwa Zaki Ibrahim, Manal El- Hamamsy
FC12.6
Persistent beneficial effects of metformin in children and adolescents with Type 1 Diabetes: Adelaide metformin randomized controlled trial follow up
Oana Maftei, Jennifer Couper, Jemma Anderson, Peter Ricci, Roger Gent, Lynne Giles, Alexia Peña
Persistent beneficial effects of metformin in children and adolescents with Type 1 Diabetes: Adelaide metformin randomized controlled trial follow up
Oana Maftei, Jennifer Couper, Jemma Anderson, Peter Ricci, Roger Gent, Lynne Giles, Alexia Peña
FC3.1
Neonatal diabetes owned to potassium channel mutation: response to sulfonylureas according to the genotype
laure garcin, anne-laure fauret, helene cavé, michel polak, jacques beltrand
Neonatal diabetes owned to potassium channel mutation: response to sulfonylureas according to the genotype
laure garcin, anne-laure fauret, helene cavé, michel polak, jacques beltrand
FC3.2
Genome-Wide Meta-Analysis identifies a novel low frequency STK39 variant of large effect on risk of Type 1 Diabetes
Vincenzo Forgetta, Despoina Manousaki, Stephanie Ross, Marie-Catherine Tessier, Luc Marchand, Hui-Qi Qu, Jonathan P. Bradfield, Struan F. A. Grant, Hakon Hakonarson, Andrew Paterson, Ciriaco Piccirillo, Constantin Polychronakos, J. Brent Richards
Genome-Wide Meta-Analysis identifies a novel low frequency STK39 variant of large effect on risk of Type 1 Diabetes
Vincenzo Forgetta, Despoina Manousaki, Stephanie Ross, Marie-Catherine Tessier, Luc Marchand, Hui-Qi Qu, Jonathan P. Bradfield, Struan F. A. Grant, Hakon Hakonarson, Andrew Paterson, Ciriaco Piccirillo, Constantin Polychronakos, J. Brent Richards
FC3.3
Pediatric patients with Type 1 Diabetes and abnormal nerve conduction studies demonstrate higher neopterin levels: potential role as a biochemical marker for peripheral neuropathy
Nancy Elbarbary, Eman Abdel Rahman Ismail, Rana Ahmed El- Hilaly, Fatma Salama Ahmed
Pediatric patients with Type 1 Diabetes and abnormal nerve conduction studies demonstrate higher neopterin levels: potential role as a biochemical marker for peripheral neuropathy
Nancy Elbarbary, Eman Abdel Rahman Ismail, Rana Ahmed El- Hilaly, Fatma Salama Ahmed
FC3.4
Is the glycaemic response from fat in meals dose dependent in children and adolescents with T1DM on intensive insulin therapy?
Susan M. O'Connell, Norma O'Toole, Conor Cronin, Chen Saat, Patrick McElduff, Bruce King, Carmel E. Smart
Is the glycaemic response from fat in meals dose dependent in children and adolescents with T1DM on intensive insulin therapy?
Susan M. O'Connell, Norma O'Toole, Conor Cronin, Chen Saat, Patrick McElduff, Bruce King, Carmel E. Smart
FC3.5
Genotype and Phenotype Correlation in Syndromic Forms of Hyperinsulinaemic Hypoglycaemia – a 10-year follow-up study in a tertiary centre
Antonia Dastamani, Eirini Kostopoulou, Emma Clements, Silvana Caiulo, Prateek Shanmugananda, Kate Morgan, Clare Gilbert, Mehul Dattani, Sarah Flanagan, Sian Ellard, Jane Hurst, Pratik Shah
Genotype and Phenotype Correlation in Syndromic Forms of Hyperinsulinaemic Hypoglycaemia – a 10-year follow-up study in a tertiary centre
Antonia Dastamani, Eirini Kostopoulou, Emma Clements, Silvana Caiulo, Prateek Shanmugananda, Kate Morgan, Clare Gilbert, Mehul Dattani, Sarah Flanagan, Sian Ellard, Jane Hurst, Pratik Shah
FC3.6
Using CRISPR/Cas9gene editing to study the molecular genetics of Congenital Hyperinsulinism
Preetha Purushothaman, Ahmad Aldossary, Ileana Guerrini, Stephen Hart, Khalid Hussain
Using CRISPR/Cas9gene editing to study the molecular genetics of Congenital Hyperinsulinism
Preetha Purushothaman, Ahmad Aldossary, Ileana Guerrini, Stephen Hart, Khalid Hussain
LB-P14
BETA-CELL FUNCTION IN CHINESE YOUNGSTERS WITH TYPE 1 DIABETES AND ASSESSMENT OF SURROGATE MARKERS OF SEVERE INSULIN DEFICIENCY
Jinna Yuan, José G B Derraik, Junfen Fu, Guanping Dong, Wayne S Cutfield, Wei Wu, Ke Huang, Youjun Jiang, Xiaochun Chen
BETA-CELL FUNCTION IN CHINESE YOUNGSTERS WITH TYPE 1 DIABETES AND ASSESSMENT OF SURROGATE MARKERS OF SEVERE INSULIN DEFICIENCY
Jinna Yuan, José G B Derraik, Junfen Fu, Guanping Dong, Wayne S Cutfield, Wei Wu, Ke Huang, Youjun Jiang, Xiaochun Chen
LB-P20
The efficacy and safety of octreotide treatment for diazoxide-unresponsive congenital hyperinsulinism in China
Bingyan Cao, Chunxiu Gong, Di Wu, Xuejun Liang, Chang Su, Min Liu, Wenjing Liu, Jiajia Chen, Xiaoqiao Li
The efficacy and safety of octreotide treatment for diazoxide-unresponsive congenital hyperinsulinism in China
Bingyan Cao, Chunxiu Gong, Di Wu, Xuejun Liang, Chang Su, Min Liu, Wenjing Liu, Jiajia Chen, Xiaoqiao Li
P1-P040
Poor metabolic control in children and adolescents with type 1 diabetes and psychiatric comorbidity
Stine M. Sildorf, Nina Breinegaard, Emilie B. Lindkvist, Janne S. Tolstrup, Kirsten A. Boisen, Grete K. Teilmann, Anne Mette Skovgaard, Jannet Svensson
Poor metabolic control in children and adolescents with type 1 diabetes and psychiatric comorbidity
Stine M. Sildorf, Nina Breinegaard, Emilie B. Lindkvist, Janne S. Tolstrup, Kirsten A. Boisen, Grete K. Teilmann, Anne Mette Skovgaard, Jannet Svensson
P1-P041
Concealment of Type 1 Diabetes in adolescence affects adherence to treatment, metabolic control, and quality of life
Judith Nir, Nir Leffler, Nessia Nagelberg, Michal Yacobovitz-Gavan, Moshe Phillip, Tal Oron
Concealment of Type 1 Diabetes in adolescence affects adherence to treatment, metabolic control, and quality of life
Judith Nir, Nir Leffler, Nessia Nagelberg, Michal Yacobovitz-Gavan, Moshe Phillip, Tal Oron
P1-P042
Risky behaviors of adolescents with Type 1 Diabetes in comparison with their healthy peers
Kyriaki Karavanaki, Betina Kandyla, Chara Tzavara, Artemis Tsitsika
Risky behaviors of adolescents with Type 1 Diabetes in comparison with their healthy peers
Kyriaki Karavanaki, Betina Kandyla, Chara Tzavara, Artemis Tsitsika
P1-P043
The effect of social burden on paediatric diabetes outcomes
Madalena Sales-Luis, Emma Smith, Michal Ajzensztejn
The effect of social burden on paediatric diabetes outcomes
Madalena Sales-Luis, Emma Smith, Michal Ajzensztejn
P1-P044
Parental anxiety about hypoglycemia of children and adolescents with Type 1 Diabetes Mellitus (T1DM) and the associated factors
Evangelia Ntinou, Anastasia Barbouni, Athanasia Liveri, Kyriaki Karavanaki
Parental anxiety about hypoglycemia of children and adolescents with Type 1 Diabetes Mellitus (T1DM) and the associated factors
Evangelia Ntinou, Anastasia Barbouni, Athanasia Liveri, Kyriaki Karavanaki
P1-P045
Management of diabetes during Ramadan fasting in children and adolescents: survey of Physicians’ perceptions and practices in the Arab Society of Paediatric Endocrinology and Diabetes (ASPED) countries
Nancy Elbarbary, Asma Deeb, Abdelhadi Habeb, Salem A. Beshyah
Management of diabetes during Ramadan fasting in children and adolescents: survey of Physicians’ perceptions and practices in the Arab Society of Paediatric Endocrinology and Diabetes (ASPED) countries
Nancy Elbarbary, Asma Deeb, Abdelhadi Habeb, Salem A. Beshyah
P1-P046
Phenotypes of diabetes and determinants of glycemic control and diabetes complications in Haitian youth living in Haiti
Marie-Pier Dumas, Michele Sainvil, Kelty Altenor, Julia Elisabeth von Oettingen
Phenotypes of diabetes and determinants of glycemic control and diabetes complications in Haitian youth living in Haiti
Marie-Pier Dumas, Michele Sainvil, Kelty Altenor, Julia Elisabeth von Oettingen
P1-P047
Smoke exposure and cardio-metabolic profile in youth with Type 1 Diabetes
Valeria Calcaterra, Hellas Cena, Luca Maria Schiamo, Chiara Montalbano, Corrado Regalbuto, Maria De Filippo, Catherine Klersy, Daniela Larizza
Smoke exposure and cardio-metabolic profile in youth with Type 1 Diabetes
Valeria Calcaterra, Hellas Cena, Luca Maria Schiamo, Chiara Montalbano, Corrado Regalbuto, Maria De Filippo, Catherine Klersy, Daniela Larizza
P1-P048
Menstrual cycle disorders in young women with Type 1 Diabetes Mellitus
Stavroula A. Paschou, Andromachi Vryonidou, Marina Melissourgou, Ioanna Kosteria, Panagiotis Anagnostis, Dimitrios G. Goulis, George P. Chrousos, Christina Kanaka-Gantenbein
Menstrual cycle disorders in young women with Type 1 Diabetes Mellitus
Stavroula A. Paschou, Andromachi Vryonidou, Marina Melissourgou, Ioanna Kosteria, Panagiotis Anagnostis, Dimitrios G. Goulis, George P. Chrousos, Christina Kanaka-Gantenbein
P1-P049
Life changing decisions due to etiological genetic diagnosis in families of children with Maturity Onset Diabetes of the Young (MODY).
Gherta Bril, Martine Vaxillaire (co-author), Noah Gruber, Kineret Mazor-Aronovitch, Michal Ben-Ami, Rachel Frumkin Ben-David, Yonathan Yeshayahu, Olivier Sand, Amelie Bonnefond, Philippe Froguel, Orit Pinhas-Hamiel
Life changing decisions due to etiological genetic diagnosis in families of children with Maturity Onset Diabetes of the Young (MODY).
Gherta Bril, Martine Vaxillaire (co-author), Noah Gruber, Kineret Mazor-Aronovitch, Michal Ben-Ami, Rachel Frumkin Ben-David, Yonathan Yeshayahu, Olivier Sand, Amelie Bonnefond, Philippe Froguel, Orit Pinhas-Hamiel
P1-P050
NBAS gene mutation causes Insulin-dependent Diabetes Mellitus in a patient with a multisystem disorder consisting immunodeficiency and extremely short stature
Sofia Giatropoulou, Rainer König, Stefan A. Wudy, Carsten Speckmann, Patrick Kury, Björn Fischer-Zirnsak, Kamrath Clemens
NBAS gene mutation causes Insulin-dependent Diabetes Mellitus in a patient with a multisystem disorder consisting immunodeficiency and extremely short stature
Sofia Giatropoulou, Rainer König, Stefan A. Wudy, Carsten Speckmann, Patrick Kury, Björn Fischer-Zirnsak, Kamrath Clemens
P1-P051
Identification of six novel mutations in monogenic diabetes and congenital hyperinsulinism and detected by targeted-exome sequencing in Korea
CHONG KUN CHEON, Ju Young Yoon
Identification of six novel mutations in monogenic diabetes and congenital hyperinsulinism and detected by targeted-exome sequencing in Korea
CHONG KUN CHEON, Ju Young Yoon
P1-P052
Genetic susceptibility to Type 1 Diabetes in children: analysis of polymorphisms rs1990760 - IFIH1, rs20541 - IL13 , rs231775 - CTLA 4
Aleksandra Goralczyk, Artur Bossowski, Joanna Goscik, Natalia Wawrusiewicz-Kurylonek, Anna Bossowska, Adam Kretowski
Genetic susceptibility to Type 1 Diabetes in children: analysis of polymorphisms rs1990760 - IFIH1, rs20541 - IL13 , rs231775 - CTLA 4
Aleksandra Goralczyk, Artur Bossowski, Joanna Goscik, Natalia Wawrusiewicz-Kurylonek, Anna Bossowska, Adam Kretowski
P1-P053
Neonatal diabetes as a first symptom of IPEX syndrom
Agnieszka Brandt, Maja Okońska, Matylda Hennig, Małgorzata Mysliwiec, Wojciech Młynarski
Neonatal diabetes as a first symptom of IPEX syndrom
Agnieszka Brandt, Maja Okońska, Matylda Hennig, Małgorzata Mysliwiec, Wojciech Młynarski
P1-P054
CpG methylation status changes within the protein tyrosine phosphatase non-receptor type 22 gene promoters in children and adolescents of Greek origin with Type 1 Diabetes
Konstantina Mouzaki, Styliani Giza, Eleni P Kotanidou, Aikaterini Fragou, Maria Taousani, Maria Eboriadou-Petikopoulou, Georgios Tzimagiorgis, Assimina Galli-Tsinopoulou
CpG methylation status changes within the protein tyrosine phosphatase non-receptor type 22 gene promoters in children and adolescents of Greek origin with Type 1 Diabetes
Konstantina Mouzaki, Styliani Giza, Eleni P Kotanidou, Aikaterini Fragou, Maria Taousani, Maria Eboriadou-Petikopoulou, Georgios Tzimagiorgis, Assimina Galli-Tsinopoulou
P1-P055
Wolfram Syndrome case with hypergonadotropic hypogonadism: A novel mutation
zeynep uzan tatlı, gul direk, mervenur hepokur, nihal hatipoglu, leyla akın, mustafa kendirci, selim kurtoglu
Wolfram Syndrome case with hypergonadotropic hypogonadism: A novel mutation
zeynep uzan tatlı, gul direk, mervenur hepokur, nihal hatipoglu, leyla akın, mustafa kendirci, selim kurtoglu
P1-P056
Different clinical findings in Maturity Onset Diabetes of the young due to B-Lymphocyte Kinase Gene Mutations
Ayla Güven, Canan Yildirimoglu
Different clinical findings in Maturity Onset Diabetes of the young due to B-Lymphocyte Kinase Gene Mutations
Ayla Güven, Canan Yildirimoglu
P1-P057
Three new gene variants (PTPRD, SYT9, and WFS1) related to Korean MODY children decrease insulin secretion in human pancreatic beta cells
Kyung-Mi Jang, Jung-Eun Moon, Su-Jeong Lee, Gi-Min Lee, Cheol-Woo Ko
Three new gene variants (PTPRD, SYT9, and WFS1) related to Korean MODY children decrease insulin secretion in human pancreatic beta cells
Kyung-Mi Jang, Jung-Eun Moon, Su-Jeong Lee, Gi-Min Lee, Cheol-Woo Ko
P1-P058
Comprehensive genetic testing shows one in five children with diabetes and non-autoimmune extra-pancreatic features have monogenic aetiology
Kashyap A Patel, Kevin Colclough, Mehmet Nuri Ozbek, Melek Yildiz, Tulay Guran, Cemil Kocyigit, Sezer Acar, Zeynep Siklar, Muge Atar, Matt B Johnson, Sarah E Flanagan, Sian Ellard, Filiz Mine Cizmecioglu, Merih Berberoglu, Korcan Demir, Gonul Catli, Serpil Bas, Teoman Akcay, Huseyin Demirbilek, Michael N Weedon, Andrew T Hattersley
Comprehensive genetic testing shows one in five children with diabetes and non-autoimmune extra-pancreatic features have monogenic aetiology
Kashyap A Patel, Kevin Colclough, Mehmet Nuri Ozbek, Melek Yildiz, Tulay Guran, Cemil Kocyigit, Sezer Acar, Zeynep Siklar, Muge Atar, Matt B Johnson, Sarah E Flanagan, Sian Ellard, Filiz Mine Cizmecioglu, Merih Berberoglu, Korcan Demir, Gonul Catli, Serpil Bas, Teoman Akcay, Huseyin Demirbilek, Michael N Weedon, Andrew T Hattersley
P1-P059
Impact of diabetes during pregnancy in women affected with GCK-MODY on neonatal health outcome.
Agnieszka Brandt, Anna Wołoszyn-Durkiewicz, Marta Buraczewska, Katarzyna Kopacz-Petranyuk, Małgorzata Myśliwiec
Impact of diabetes during pregnancy in women affected with GCK-MODY on neonatal health outcome.
Agnieszka Brandt, Anna Wołoszyn-Durkiewicz, Marta Buraczewska, Katarzyna Kopacz-Petranyuk, Małgorzata Myśliwiec
P1-P060
IPEX as a result of mutations in FOXP3 two case reports and review of the literature
qiong zhu, chunlin wang
IPEX as a result of mutations in FOXP3 two case reports and review of the literature
qiong zhu, chunlin wang
P1-P061
The prevalence of autonomic and peripheral neuropathy in children and adolescents with Type 1 Diabetic Mellitus (T1D) and its association with the homozygous status of Z-2/Z-2 polymorphism of the aldose reductase gene (AKR1B1) in the polyol pathway
Dimitra Kallinikou, Charalampos Tsentidis, Kyriaki Kekou, Maria Louraki, Christina Kanaka-Gantenbein, Emmanouil Kanavakis, Kyriaki Karavanaki
The prevalence of autonomic and peripheral neuropathy in children and adolescents with Type 1 Diabetic Mellitus (T1D) and its association with the homozygous status of Z-2/Z-2 polymorphism of the aldose reductase gene (AKR1B1) in the polyol pathway
Dimitra Kallinikou, Charalampos Tsentidis, Kyriaki Kekou, Maria Louraki, Christina Kanaka-Gantenbein, Emmanouil Kanavakis, Kyriaki Karavanaki
P1-P062
Establishment of iron overload insulin cell model and the effect induced by iron overload on oxidative stress
Lina ZHANG, Liyang LIANG, Zhe MENG, Lele HOU, Zulin LIU
Establishment of iron overload insulin cell model and the effect induced by iron overload on oxidative stress
Lina ZHANG, Liyang LIANG, Zhe MENG, Lele HOU, Zulin LIU
P1-P063
Glucose intolerance in survivors of childhood hematologic disorders
Seonhwa Lee, Yujung Choi, Seul ki Kim, Moonbae Ahn, Min-Kyo Chun, Shinhee Kim, Wonkyoung Cho, Kyoungsoon Cho, Minho Jung, Byungkyu Suh
Glucose intolerance in survivors of childhood hematologic disorders
Seonhwa Lee, Yujung Choi, Seul ki Kim, Moonbae Ahn, Min-Kyo Chun, Shinhee Kim, Wonkyoung Cho, Kyoungsoon Cho, Minho Jung, Byungkyu Suh
P1-P064
EFFICACY OF MECASERMIN TREATMENT AND LONG-TERM SURVIVAL IN A CHILD WITH LEPRECHAUNISM
Maria Cristina Maggio, Fabrizio Barbetti, Marcello Vitaliti, Saveria Sabrina Ragusa, Giuliana Vitaliti, Giovanni Corsello
EFFICACY OF MECASERMIN TREATMENT AND LONG-TERM SURVIVAL IN A CHILD WITH LEPRECHAUNISM
Maria Cristina Maggio, Fabrizio Barbetti, Marcello Vitaliti, Saveria Sabrina Ragusa, Giuliana Vitaliti, Giovanni Corsello
P1-P065
Evaluation of diabetes related complications and endothelial dysfunction in adolescents with Type 1 Diabetes
Nehad Metwally, Alan Macken, Myra O'Regan, Helen Fitzgerald, Ciara McDonnell, Clodagh S O'Gorman, Eleanor Molloy, Edna F Roche
Evaluation of diabetes related complications and endothelial dysfunction in adolescents with Type 1 Diabetes
Nehad Metwally, Alan Macken, Myra O'Regan, Helen Fitzgerald, Ciara McDonnell, Clodagh S O'Gorman, Eleanor Molloy, Edna F Roche
P1-P066
Complexities in the management of New-Onset Diabetes After Transplantation (NODAT) in an adolescent with Senior-Loken syndrome
Philippa Bowen, Alison Garde, Rebekah Adams, Sophie Velleman, Carol Inward, Dinesh Giri
Complexities in the management of New-Onset Diabetes After Transplantation (NODAT) in an adolescent with Senior-Loken syndrome
Philippa Bowen, Alison Garde, Rebekah Adams, Sophie Velleman, Carol Inward, Dinesh Giri
P1-P067
Insulin resistance parameters in children who were born very preterm and adequate for gestational age
Hernán García, Helena Poggi, Mónica Arancibia, Soledad Peredo, Claudia Trincado, Rosario Moore, Ivonne D'Apremont, Daniela Andrade, Sofía Sifaqui, JT Ossa, Carmen Campino, Cristian Carvajal, Carlos Fardella, René Baudrand, Sandra Solari, Fidel Allende, Alejandro Martínez-Aguayo
Insulin resistance parameters in children who were born very preterm and adequate for gestational age
Hernán García, Helena Poggi, Mónica Arancibia, Soledad Peredo, Claudia Trincado, Rosario Moore, Ivonne D'Apremont, Daniela Andrade, Sofía Sifaqui, JT Ossa, Carmen Campino, Cristian Carvajal, Carlos Fardella, René Baudrand, Sandra Solari, Fidel Allende, Alejandro Martínez-Aguayo
P1-P068
Impact on final height of functional insulin-therapy in type 1 diabetes mellitus pediatric patients – experience from a Portuguese Pediatric Endocrinology Unit
Joana Serra-Caetano, Ana Lopes Dias, Ana Ferraz, Adriana Lages, Patrícia Miranda, Rita Cardoso, Isabel Dinis, Alice Mirante
Impact on final height of functional insulin-therapy in type 1 diabetes mellitus pediatric patients – experience from a Portuguese Pediatric Endocrinology Unit
Joana Serra-Caetano, Ana Lopes Dias, Ana Ferraz, Adriana Lages, Patrícia Miranda, Rita Cardoso, Isabel Dinis, Alice Mirante
P1-P069
Triglyceride glucose index as a predictor of impaired glucose tolerance in overweight and obese adolescents
Voraluck Phatarakijnirund, Chula Kooanantkul, Warissara Sanor, Nawaporn Numbenjapon, Pacharin Mungklarat
Triglyceride glucose index as a predictor of impaired glucose tolerance in overweight and obese adolescents
Voraluck Phatarakijnirund, Chula Kooanantkul, Warissara Sanor, Nawaporn Numbenjapon, Pacharin Mungklarat
P1-P070
Birth weight in offsprings of mothers with gestational diabetes mellitus due to mutations in GCK gene
Natalia Zubkova, Fatima Burumkulova, Vasily Petrukhin, Margarita Plechanova, Anton Panov, Victoria Ulyatovskaya, Nina Makretskaya, Anatoliy Tiulpakov
Birth weight in offsprings of mothers with gestational diabetes mellitus due to mutations in GCK gene
Natalia Zubkova, Fatima Burumkulova, Vasily Petrukhin, Margarita Plechanova, Anton Panov, Victoria Ulyatovskaya, Nina Makretskaya, Anatoliy Tiulpakov
P1-P071
Review and audit of diabetes control in children and young people with diabetes using the FreestyleLibre Flash Glucose Scanning System (FGS)
Aisha Zahid, Pooja Sachdev, Louise Denvir, Tabitha Randell, Josephine Drew
Review and audit of diabetes control in children and young people with diabetes using the FreestyleLibre Flash Glucose Scanning System (FGS)
Aisha Zahid, Pooja Sachdev, Louise Denvir, Tabitha Randell, Josephine Drew
P1-P072
Increasing use of continuous glucose monitoring (CGM) among youth with Type 1 Diabetes (T1D): icomparison of youth from the T1D Exchange (T1DX) and the DPV Initiative
Kellee Miller, Julia Hermann, David Maahs, Sabine Hofer, Nicole Foster, Reinhard Holl
Increasing use of continuous glucose monitoring (CGM) among youth with Type 1 Diabetes (T1D): icomparison of youth from the T1D Exchange (T1DX) and the DPV Initiative
Kellee Miller, Julia Hermann, David Maahs, Sabine Hofer, Nicole Foster, Reinhard Holl
P1-P073
Efficacy of real-time continuous glucose monitoring in Type 1 Diabetic pre-school and school children treated with multiple daily injections
RICCARDO SCHIAFFINI, NOVELLA RAPINI, GRAZIA PELLICANO, PATRIZIA IPPOLITA PATERA, PAOLO CIAMPALINI, MARIA CRISTINA MATTEOLI, ANNALISA DEODATI, STEFANO CIANFARANI
Efficacy of real-time continuous glucose monitoring in Type 1 Diabetic pre-school and school children treated with multiple daily injections
RICCARDO SCHIAFFINI, NOVELLA RAPINI, GRAZIA PELLICANO, PATRIZIA IPPOLITA PATERA, PAOLO CIAMPALINI, MARIA CRISTINA MATTEOLI, ANNALISA DEODATI, STEFANO CIANFARANI
P1-P074
Catheter site selection and anthropometric measurements at subjects with type 1 diabetes and continuous subcutaneous insulin infusion
MARIA XATZIPSALTI, MARINA VAKAKI, LIDA MENTESIDOU, AFRODITI KOURTI, KONSTANTINA PATOUNI, ANNA CHOUNDALA, LELA STAMOGIANNOU, ANDRIANI VAZEOU
Catheter site selection and anthropometric measurements at subjects with type 1 diabetes and continuous subcutaneous insulin infusion
MARIA XATZIPSALTI, MARINA VAKAKI, LIDA MENTESIDOU, AFRODITI KOURTI, KONSTANTINA PATOUNI, ANNA CHOUNDALA, LELA STAMOGIANNOU, ANDRIANI VAZEOU
P1-P075
Open source artificial pancreas systems used from Bulgarian children and young people with diabetes
Maia Konstantinova, Milos Kozak, Radoslav Radev, Rositza Pandova, Hristina Dimova, Rumen Georgiev
Open source artificial pancreas systems used from Bulgarian children and young people with diabetes
Maia Konstantinova, Milos Kozak, Radoslav Radev, Rositza Pandova, Hristina Dimova, Rumen Georgiev
P1-P076
National Survey of usage of continuous glucose monitoring in children and adolescents at non reimbursed setting
Yuliya Bazdarska, Violeta Iotova, Vilhelm Mladenov, Veselin Boyadzhiev, Chayka Petrova, Irina Halvadjian, Radka Savova, Galina Popova, Reni Koleva, Mariyana Moskova, Nartsis Kaleva, Diana Nedyalkova
National Survey of usage of continuous glucose monitoring in children and adolescents at non reimbursed setting
Yuliya Bazdarska, Violeta Iotova, Vilhelm Mladenov, Veselin Boyadzhiev, Chayka Petrova, Irina Halvadjian, Radka Savova, Galina Popova, Reni Koleva, Mariyana Moskova, Nartsis Kaleva, Diana Nedyalkova
P1-P077
Additional insulin is necessary to prevent rise in blood glucose after fat-protein-rich meals in Type 1 Diabetes
Roland Schweizer, Susann Herrlich, Martina Lösch-Binder, Michaela Glökler, Magdalena Heimgärtner, Franziska Liebrich, Katja Meßner, Tina Muckenhaupt, Angelika Schneider, Julian Ziegler, Andreas Neu
Additional insulin is necessary to prevent rise in blood glucose after fat-protein-rich meals in Type 1 Diabetes
Roland Schweizer, Susann Herrlich, Martina Lösch-Binder, Michaela Glökler, Magdalena Heimgärtner, Franziska Liebrich, Katja Meßner, Tina Muckenhaupt, Angelika Schneider, Julian Ziegler, Andreas Neu
P1-P078
Efficacy of autologous hematopoietic stem cell transplantation in the treatment of childhood type 1 diabetesEfficacy of autologous hematopoietic stem cell transplantation in the treatment of childhood type 1 diabetes
Zhou Pei, Chengjun Sun, Hongsheng Wang, Xiaowen Zhai, Feihong Luo
Efficacy of autologous hematopoietic stem cell transplantation in the treatment of childhood type 1 diabetesEfficacy of autologous hematopoietic stem cell transplantation in the treatment of childhood type 1 diabetes
Zhou Pei, Chengjun Sun, Hongsheng Wang, Xiaowen Zhai, Feihong Luo
P1-P079
A novel SLCA16A1 mutation in an infant with hypoglycemia and severe metabolic ketoacidosis
Reem Hasnah, Sara Al-Khawaga, Saras Saraswathi, Basma Haris, Amira Saeed, Sanaa Sharari, Idris Mohammed, Khalid Hussain
A novel SLCA16A1 mutation in an infant with hypoglycemia and severe metabolic ketoacidosis
Reem Hasnah, Sara Al-Khawaga, Saras Saraswathi, Basma Haris, Amira Saeed, Sanaa Sharari, Idris Mohammed, Khalid Hussain
P1-P080
Successful transition to sulfonylurea therapy in infant with neonatal diabetes, developmental delay, epilepsy (DEND syndrome) due to F132L ABCC8 mutation
Yulia Tikhonovich, Natalia Zubkova, Elena Petryaikina, Irina Ribkina, Irina Garyaeva, Anatoly Tiulpakov
Successful transition to sulfonylurea therapy in infant with neonatal diabetes, developmental delay, epilepsy (DEND syndrome) due to F132L ABCC8 mutation
Yulia Tikhonovich, Natalia Zubkova, Elena Petryaikina, Irina Ribkina, Irina Garyaeva, Anatoly Tiulpakov
P1-P081
ZFP57-associated transient neonatal diabetes is responsive to oral sulfonylurea treatment
Christina Reinauer, Annemarie Jonasson, Stefani Harmsen, Pierre Debinski, Volker Soditt, Sonia van Afferden, Ertan Mayatepek, Carsten Bergmann, Thomas Meissner, Sebastian Kummer
ZFP57-associated transient neonatal diabetes is responsive to oral sulfonylurea treatment
Christina Reinauer, Annemarie Jonasson, Stefani Harmsen, Pierre Debinski, Volker Soditt, Sonia van Afferden, Ertan Mayatepek, Carsten Bergmann, Thomas Meissner, Sebastian Kummer
P1-P082
The comparison of the occurrence of beta cells autoantibody and regulatory T cells (CD4+CD25+FoxP3+) in patients with type 1 diabetes mellitus, their siblings and healthy children
Joanna Sieniawska, Aleksandra Krzewska, Iwona Ben-Skowronek
The comparison of the occurrence of beta cells autoantibody and regulatory T cells (CD4+CD25+FoxP3+) in patients with type 1 diabetes mellitus, their siblings and healthy children
Joanna Sieniawska, Aleksandra Krzewska, Iwona Ben-Skowronek
P1-P083
HERV-W-Env protein expression in pediatric type 1 diabetes patients
Thérèse Bouthors, Eglantine Elowe-Gruau, Patricia Diaz-Escagedo, Maria-Christina Antoniou, Sophie Stoppa-Vaucher, Sandrine Levet, Julie Medina, Amandine Demolder, Hervé Perron, Michael Hauschild
HERV-W-Env protein expression in pediatric type 1 diabetes patients
Thérèse Bouthors, Eglantine Elowe-Gruau, Patricia Diaz-Escagedo, Maria-Christina Antoniou, Sophie Stoppa-Vaucher, Sandrine Levet, Julie Medina, Amandine Demolder, Hervé Perron, Michael Hauschild
P1-P084
The comparison of the occurrence of beta cells autoantibody and natural killer cells in patients with type 1 diabetes mellitus, their siblings and healthy children
Joanna Sieniawska, Aleksandra Krzewska, Iwona Ben-Skowronek
The comparison of the occurrence of beta cells autoantibody and natural killer cells in patients with type 1 diabetes mellitus, their siblings and healthy children
Joanna Sieniawska, Aleksandra Krzewska, Iwona Ben-Skowronek
P1-P085
T – and B-Lymphocytes levels in children with Type 1 Diabetes in association with Candida infection
Stanimira Elkina, Svetla Blajeva, Irina Halvadzhiyan, Venetziya Botzova, Chayka Petrova
T – and B-Lymphocytes levels in children with Type 1 Diabetes in association with Candida infection
Stanimira Elkina, Svetla Blajeva, Irina Halvadzhiyan, Venetziya Botzova, Chayka Petrova
P1-P086
Coincidence of newly diagnosed Type 1 Diabetes Mellitus with Enteroviruses and respiratory tract viruses
Murat Karaoglan, Fahriye Eksi, Mehmet Keskin, İlkay Karaoglan
Coincidence of newly diagnosed Type 1 Diabetes Mellitus with Enteroviruses and respiratory tract viruses
Murat Karaoglan, Fahriye Eksi, Mehmet Keskin, İlkay Karaoglan
P1-P087
Investigation into β-cell adaptation during puberty
Anne-Laure Castell, Mélanie Ethier, Grace Fergusson, Julien Ghislain, Vincent Poitout
Investigation into β-cell adaptation during puberty
Anne-Laure Castell, Mélanie Ethier, Grace Fergusson, Julien Ghislain, Vincent Poitout
P1-P088
The shape of the glucose curve and time to glucose peak during an oral glucose tolerance test as indicators of beta cell function in obese adolescents
Lavinia La Grasta Sabolić, Gordana Stipančić, Marija Požgaj Šepec
The shape of the glucose curve and time to glucose peak during an oral glucose tolerance test as indicators of beta cell function in obese adolescents
Lavinia La Grasta Sabolić, Gordana Stipančić, Marija Požgaj Šepec
P1-P089
Features of T2DM in adolescents with low titer of ICA and IAA
Irina Eremina, Tamara Kuraeva, Lubov Zilberman, Valentina Peterkova
Features of T2DM in adolescents with low titer of ICA and IAA
Irina Eremina, Tamara Kuraeva, Lubov Zilberman, Valentina Peterkova
P1-P090
Increasing trend of fasting plasma glucose levels and impaired fasting glucose in non-diabetic Korean youth and young adults:a nationally representative population-based study
JIEUN LEE, Young Ah Lee, Jae Hyun Kim, Seong Yong Lee, Choong Ho Shin, Sei Won Yang
Increasing trend of fasting plasma glucose levels and impaired fasting glucose in non-diabetic Korean youth and young adults:a nationally representative population-based study
JIEUN LEE, Young Ah Lee, Jae Hyun Kim, Seong Yong Lee, Choong Ho Shin, Sei Won Yang
P1-P091
Screening for T2D in high risk Egyptian children and adolescents using strip HbA1c and OGTT
Mona Hafez, Noha Musa, Mona Mansour, Heba Hamdy
Screening for T2D in high risk Egyptian children and adolescents using strip HbA1c and OGTT
Mona Hafez, Noha Musa, Mona Mansour, Heba Hamdy
P1-P092
Association of the sizes and composition of HDL with hepatic steatosis in adolescents with Type 2 Diabetes (T2D)
Jose Antonio Orozco Morales, Margarita Torres Tamayo, Aída Medina Urrutia, Juan Gabriel Juárez Rojas, Juan Reyes Barrera, Esteban Jorge Galarza, Pilar Dies Suárez, Patricia Medina Bravo
Association of the sizes and composition of HDL with hepatic steatosis in adolescents with Type 2 Diabetes (T2D)
Jose Antonio Orozco Morales, Margarita Torres Tamayo, Aída Medina Urrutia, Juan Gabriel Juárez Rojas, Juan Reyes Barrera, Esteban Jorge Galarza, Pilar Dies Suárez, Patricia Medina Bravo
P2-P060
Incidence of Childhood Type 1 and Type 2 Diabetes Mellitus in Qatar between 2012- 2016
Fawziya Alyafei, Ashraf Soliman, Fawziya Alkhalaf, Reem Waseef, Anas Abdulkayoum, Ahmed sayed, Nagwa eldarsy, aml sabt
Incidence of Childhood Type 1 and Type 2 Diabetes Mellitus in Qatar between 2012- 2016
Fawziya Alyafei, Ashraf Soliman, Fawziya Alkhalaf, Reem Waseef, Anas Abdulkayoum, Ahmed sayed, Nagwa eldarsy, aml sabt
P2-P061
The prevalence of double diabetes in children and adolescents in Qatar
Ashraf Soliman, Fawzia Alyafei, Reem Wasfy, Nagwa Aldarsy
The prevalence of double diabetes in children and adolescents in Qatar
Ashraf Soliman, Fawzia Alyafei, Reem Wasfy, Nagwa Aldarsy
P2-P062
Prevalence of Diabetes Type 1 and type 2 in children and adults in Kazakhstan in 2016
Akmaral Nurbekova, Aigul Balmuchanova, Svetlana Ten, Amrit Bhangoo
Prevalence of Diabetes Type 1 and type 2 in children and adults in Kazakhstan in 2016
Akmaral Nurbekova, Aigul Balmuchanova, Svetlana Ten, Amrit Bhangoo
P2-P063
Detection of the pathogenic genes in the diagnosis and treatment of hyperglycemia infants and children
Zhuhui Zhao, Ruoqian Cheng, Li Xi, Xiaojing Li, Miaoying Zhang, Zhou Pei, Chengjun Sun
Detection of the pathogenic genes in the diagnosis and treatment of hyperglycemia infants and children
Zhuhui Zhao, Ruoqian Cheng, Li Xi, Xiaojing Li, Miaoying Zhang, Zhou Pei, Chengjun Sun
P2-P064
Early diagnosis of Diabetes Type 2 in children with progeria syndromes
Martin Bald, Kirsten Timmermann, Tanja Wadien, Eva Krähling, Martin Holder
Early diagnosis of Diabetes Type 2 in children with progeria syndromes
Martin Bald, Kirsten Timmermann, Tanja Wadien, Eva Krähling, Martin Holder
P2-P065
Transient Neonatal Diabetes Mellitus due to not described mutation in ABCC8 gene with different behaviour in affected family members
MARIA ANGELES SANTOS MATA, IRENE PILAR FERNANDEZ VISERAS, ISABEL TORRES BAREA, LUIS CASTAÑO GONZALEZ
Transient Neonatal Diabetes Mellitus due to not described mutation in ABCC8 gene with different behaviour in affected family members
MARIA ANGELES SANTOS MATA, IRENE PILAR FERNANDEZ VISERAS, ISABEL TORRES BAREA, LUIS CASTAÑO GONZALEZ
P2-P066
Prothrombin Gene 20210A mutation heterozygosity and MTHFR Gene C677T mutation homozygosity detected in a male toddler experiencing femoral venous thrombosis during diabetic ketoacidosis
Angeliki N Kleisarchaki, Styliani Giza, Olga Nikolaidou, Konstantina Mouzaki, Eleni P Kotanidou, Eleni Litou, Vasiliki Rengina Tsinopoulou, Emmanouil Papadakis, Assimina Galli-Tsinopoulou
Prothrombin Gene 20210A mutation heterozygosity and MTHFR Gene C677T mutation homozygosity detected in a male toddler experiencing femoral venous thrombosis during diabetic ketoacidosis
Angeliki N Kleisarchaki, Styliani Giza, Olga Nikolaidou, Konstantina Mouzaki, Eleni P Kotanidou, Eleni Litou, Vasiliki Rengina Tsinopoulou, Emmanouil Papadakis, Assimina Galli-Tsinopoulou
P2-P067
Frequency of occurrence of MODY in the population of diabetic patients in St. Petersburg
Mariia Turkunova, Elena Bashnina, Olga Berseneva, Oleg Glotov, Andrei Glotov, Elena Serebryakova
Frequency of occurrence of MODY in the population of diabetic patients in St. Petersburg
Mariia Turkunova, Elena Bashnina, Olga Berseneva, Oleg Glotov, Andrei Glotov, Elena Serebryakova
P2-P068
Acute painful diabetic neuropathy (APDN) in a boy with Type 1 Diabetes
Nataliia Muz, Viktoriia Pakhomova, Nataliia Sprinchuk
Acute painful diabetic neuropathy (APDN) in a boy with Type 1 Diabetes
Nataliia Muz, Viktoriia Pakhomova, Nataliia Sprinchuk
P2-P069
Features of Japanese patients with early-onset, MODY-like diabetes without mutations in the major MODY genes
Tohru Yorifuji, Rie Kawakita, Shinji Higuchi, Yuki Yamada, Maki Ohyachi, Kana Matsumura
Features of Japanese patients with early-onset, MODY-like diabetes without mutations in the major MODY genes
Tohru Yorifuji, Rie Kawakita, Shinji Higuchi, Yuki Yamada, Maki Ohyachi, Kana Matsumura
P2-P070
Frequency and etiologic spectrum of monogenic diabetes in pediatric diabetes in a single academic center
Jin-Ho Choi, Go Hun Seo, Arum Oh, Gu-Hwan Kim, Han-Wook Yoo
Frequency and etiologic spectrum of monogenic diabetes in pediatric diabetes in a single academic center
Jin-Ho Choi, Go Hun Seo, Arum Oh, Gu-Hwan Kim, Han-Wook Yoo
P2-P071
Clinical details, molecular genetic analysisand clinical pheonotype correlation of 14 patients with neonatal diabetes from the South India – a single centre experience
SRI NAGESH.V, ANDREW HATTERSLEY, SIAN ELLARD, BIPIN SETHI, ELISA DE FRANCO, SARAH FLANAGAN, JAYNE HOUGHTON, VENKATESHWARLU M, HARSH PAREKH, VAIBHAV DUKLE, JAYANT KELWADE, ALTAF NASEEM, RAVISHANKAR KANITHI, RAVI KUMAR NALLI
Clinical details, molecular genetic analysisand clinical pheonotype correlation of 14 patients with neonatal diabetes from the South India – a single centre experience
SRI NAGESH.V, ANDREW HATTERSLEY, SIAN ELLARD, BIPIN SETHI, ELISA DE FRANCO, SARAH FLANAGAN, JAYNE HOUGHTON, VENKATESHWARLU M, HARSH PAREKH, VAIBHAV DUKLE, JAYANT KELWADE, ALTAF NASEEM, RAVISHANKAR KANITHI, RAVI KUMAR NALLI
P2-P072
Syndromic patients with negative islet autoantibodies should be tested for Mongenic Diabetes: lessons from patient with TRMT10A mutation
Zeynep SIKLAR, Kevin Colclough, Kashyap A Patel, Tuğba Çetin, Merih Berberoğlu
Syndromic patients with negative islet autoantibodies should be tested for Mongenic Diabetes: lessons from patient with TRMT10A mutation
Zeynep SIKLAR, Kevin Colclough, Kashyap A Patel, Tuğba Çetin, Merih Berberoğlu
P2-P073
A novel mutation in PHKA2: Idiopathic ketotic hypoglycaemia may represent mild GSDIXa
Anne Benner Flejsborg, Klaus Brusgaard, Carsten Pedersen, Anja L. Frederiksen, Henrik T. Christesen
A novel mutation in PHKA2: Idiopathic ketotic hypoglycaemia may represent mild GSDIXa
Anne Benner Flejsborg, Klaus Brusgaard, Carsten Pedersen, Anja L. Frederiksen, Henrik T. Christesen
P2-P074
The application of Next Generation Sequencing MODY Gene Panel in Greek patients
Elizabeth Tatsi, Penelopi Smirnaki, Panagiota Triantafilou, Kyriaki Tsiroukidou, Kalliopi Kotsa, Vaia Lambadiari, George Chrousos, Christina Kanaka-Gantenbein, Amalia Sertedaki
The application of Next Generation Sequencing MODY Gene Panel in Greek patients
Elizabeth Tatsi, Penelopi Smirnaki, Panagiota Triantafilou, Kyriaki Tsiroukidou, Kalliopi Kotsa, Vaia Lambadiari, George Chrousos, Christina Kanaka-Gantenbein, Amalia Sertedaki
P2-P075
Type 5 Monogenic Diabetes. Reportof 7 cases
Mogas Eduard, Pacheco Rosa, Yeste Diego, Campos Ariadna, Castaño Luis, Clemente María
Type 5 Monogenic Diabetes. Reportof 7 cases
Mogas Eduard, Pacheco Rosa, Yeste Diego, Campos Ariadna, Castaño Luis, Clemente María
P2-P076
Novel GATA6-mutation in a boy with neonatal diabetes and diaphragmatic hernia
Odile Christin Gaisl, Daniel Konrad, Katharina Steindl, Mariarosaria Lang-Muritano
Novel GATA6-mutation in a boy with neonatal diabetes and diaphragmatic hernia
Odile Christin Gaisl, Daniel Konrad, Katharina Steindl, Mariarosaria Lang-Muritano
P2-P077
Clinical and genetic characterizations of maturity onset diabetes of the young: single center results
Ayla Güven, Canan Yıldırımoglu
Clinical and genetic characterizations of maturity onset diabetes of the young: single center results
Ayla Güven, Canan Yıldırımoglu
P2-P078
Protein and fat effects on post - prandial glucose responses among Egyptian children and adolescents with Type 1 Diabetes Mellitus
Noha Arafa, Mona Hafez, Ghada Anwar, Marise Abdou, Rania Ibrahim
Protein and fat effects on post - prandial glucose responses among Egyptian children and adolescents with Type 1 Diabetes Mellitus
Noha Arafa, Mona Hafez, Ghada Anwar, Marise Abdou, Rania Ibrahim
P2-P079
Amino acids plasma profile in children with type 1 diabetes
Teodoro Durá-Travé, Ernesto Cortes-Castell, Manuel Moya-Benavent, María Jesús Chueca-Guindulain, Sara Berrade-Zubiri, Javier Nogueira-López
Amino acids plasma profile in children with type 1 diabetes
Teodoro Durá-Travé, Ernesto Cortes-Castell, Manuel Moya-Benavent, María Jesús Chueca-Guindulain, Sara Berrade-Zubiri, Javier Nogueira-López
P2-P080
Betatrophin as a new biomarker of Type 1 Diabetes Mellitus in paediatrics
Laura Bosch i Ara, Adria Villalba, Marta Murillo, Mireia Fonolleda, Federico Vazquez, Silvia Rodríguez-Fernández, Marta Vives-Pi, Joan Bel
Betatrophin as a new biomarker of Type 1 Diabetes Mellitus in paediatrics
Laura Bosch i Ara, Adria Villalba, Marta Murillo, Mireia Fonolleda, Federico Vazquez, Silvia Rodríguez-Fernández, Marta Vives-Pi, Joan Bel
P2-P081
Vitamin D status among children and adolescent with T1DM
Mohamed Firas Khudhur, Waleed Jasim
Vitamin D status among children and adolescent with T1DM
Mohamed Firas Khudhur, Waleed Jasim
P2-P082
IGF-1 relationship with growth velocity in precocious puberty with GnRHa treatment
nursel muratoglu sahin, semra cetinkaya, senay savas erdeve, zehra aycan
IGF-1 relationship with growth velocity in precocious puberty with GnRHa treatment
nursel muratoglu sahin, semra cetinkaya, senay savas erdeve, zehra aycan
P2-P083
Relation between hypomagnesemia and increased level of HbA1c in patients with diabetes mellitus
Seokjin Kang, Heung Sik Kim
Relation between hypomagnesemia and increased level of HbA1c in patients with diabetes mellitus
Seokjin Kang, Heung Sik Kim
P2-P084
PID1 alters antilipolytic action of insulin and increases lipolysis via Inhibited the activation of AKT/PKA Pathway
chun yin, yan xiao
PID1 alters antilipolytic action of insulin and increases lipolysis via Inhibited the activation of AKT/PKA Pathway
chun yin, yan xiao
P2-P085
The efficacy of tri-ponderal mass index and body mass index in estimating insulin resistance, hyperlipidemia and impaired liver enzymes during childhood and adolescents
nese akcan, Moaaz Obyed, Jana Salem, Ruveyde Bundak
The efficacy of tri-ponderal mass index and body mass index in estimating insulin resistance, hyperlipidemia and impaired liver enzymes during childhood and adolescents
nese akcan, Moaaz Obyed, Jana Salem, Ruveyde Bundak
P2-P087
Translating the A1C assay into estimated average glucose values in children with Type 1 Diabetes Mellitus
Ahmed Mohamed Sayed, Fawzia Alyafei, Ashraf Soliman, Mona Algamal
Translating the A1C assay into estimated average glucose values in children with Type 1 Diabetes Mellitus
Ahmed Mohamed Sayed, Fawzia Alyafei, Ashraf Soliman, Mona Algamal
P2-P088
Relationship between residual endogenous insulin secretion and glycemic control in Japanese children and adolescents with Type 1 Diabetes
Ikuma Musha, Hiroshi Kawana, Junya Akatsuka, Akira Ohtake, Shin Amemiya, Toru Kikuchi
Relationship between residual endogenous insulin secretion and glycemic control in Japanese children and adolescents with Type 1 Diabetes
Ikuma Musha, Hiroshi Kawana, Junya Akatsuka, Akira Ohtake, Shin Amemiya, Toru Kikuchi
P2-P089
A curious case of persistent lactic acidosis in a child with diabetic ketoacidosis
Andrew Sng, Nicholas Ng, Chin Hui-Lin, Yvonne Lim
A curious case of persistent lactic acidosis in a child with diabetic ketoacidosis
Andrew Sng, Nicholas Ng, Chin Hui-Lin, Yvonne Lim
P2-P090
An unusual case of an exclusively vegan child with diabetic acidosis
Maria Xatzipsalti, Sotiris Konstantakopoulos, Afroditi Kourti, Maria Anastasoudi, Olga Fafoula, Christina Limperatou, Lela Stamogiannou, Andriani Vazeou
An unusual case of an exclusively vegan child with diabetic acidosis
Maria Xatzipsalti, Sotiris Konstantakopoulos, Afroditi Kourti, Maria Anastasoudi, Olga Fafoula, Christina Limperatou, Lela Stamogiannou, Andriani Vazeou
P2-P091
“HLA-DQ genotyping in patients with Type 1 diabetes mellitus and celiac disease”
Neeraj Agrawal, Shweta Bhandari, Andleeb Zehra Andleeb, Usha Singh
“HLA-DQ genotyping in patients with Type 1 diabetes mellitus and celiac disease”
Neeraj Agrawal, Shweta Bhandari, Andleeb Zehra Andleeb, Usha Singh
P2-P092
Hypertriglyceridemia in Type 1 Diabetes children during diabetic ketoacidosis; relation to DKA severity and glycemic control
Lubna Fawaz, Noha Musa, Sahar AbdelAtty, Ahmed Nassef
Hypertriglyceridemia in Type 1 Diabetes children during diabetic ketoacidosis; relation to DKA severity and glycemic control
Lubna Fawaz, Noha Musa, Sahar AbdelAtty, Ahmed Nassef
P2-P093
Acute mononeuropathy in an 8-year-old-girl with newly diagnosed Type 1 Diabetes
Styliani Giza, Eleni Litou, Eleni P Kotanidou, Panagiotis Koliatos, Angeliki N Kleisarchaki, Tasos Tzirtzipis, Vasiliki Rengina Tsinopoulou, Athanassios Tihalas, Athanassios Evangeliou, Assimina Galli-Tsinopoulou
Acute mononeuropathy in an 8-year-old-girl with newly diagnosed Type 1 Diabetes
Styliani Giza, Eleni Litou, Eleni P Kotanidou, Panagiotis Koliatos, Angeliki N Kleisarchaki, Tasos Tzirtzipis, Vasiliki Rengina Tsinopoulou, Athanassios Tihalas, Athanassios Evangeliou, Assimina Galli-Tsinopoulou
P2-P094
HLA- G gene promoter methylation status in children and adolescents with Type 1 Diabetes
Konstantina Mouzaki, Eleni P Kotanidou, Aikaterini Fragou, Styliani Giza, Maria Taousani, Anastasios Serbis, Maria Eboriadou-Petikopoulou, Georgios Tzimagiorgis, Assimina Galli-Tsinopoulou
HLA- G gene promoter methylation status in children and adolescents with Type 1 Diabetes
Konstantina Mouzaki, Eleni P Kotanidou, Aikaterini Fragou, Styliani Giza, Maria Taousani, Anastasios Serbis, Maria Eboriadou-Petikopoulou, Georgios Tzimagiorgis, Assimina Galli-Tsinopoulou
P2-P095
Impaired adrenal function in pediatric patients with Diabetes Mellitus type 1 evaluated with low-dose Synacthen test
Marialena Kalymniou, Meropi Dimitriadou, Aris Slavakis, Athanasios Christoforidis
Impaired adrenal function in pediatric patients with Diabetes Mellitus type 1 evaluated with low-dose Synacthen test
Marialena Kalymniou, Meropi Dimitriadou, Aris Slavakis, Athanasios Christoforidis
P2-P096
The incorporation of available technologies for diabetes care among different worldwide centers: The ESPE/ISPAD Working Group on Diabetes Technology Survey
Klemen Dovc, Shlomit Shalitin, Ragnar Hanas, Charlotte Boughton, Gianluca Musolino, Tadej Battelino, Revital Nimri, Moshe Phillip
The incorporation of available technologies for diabetes care among different worldwide centers: The ESPE/ISPAD Working Group on Diabetes Technology Survey
Klemen Dovc, Shlomit Shalitin, Ragnar Hanas, Charlotte Boughton, Gianluca Musolino, Tadej Battelino, Revital Nimri, Moshe Phillip
P2-P097
Higher percentage of insulin pump users at Isle of Man (IOM) – Two years observational data
Vineet Varshney, Anna Kurien, Pam Unsworth, Catherine Wallinger, Arundoss Gangadharan
Higher percentage of insulin pump users at Isle of Man (IOM) – Two years observational data
Vineet Varshney, Anna Kurien, Pam Unsworth, Catherine Wallinger, Arundoss Gangadharan
P2-P098
Use of Continuous Glucose Monitoring systems in the early detection and management of Cystic Fibrosis Related Diabetes in children
Akinsola Ogundiya, Marion Martin, Nancy Katkat, Laura Thomas, Joanne Russell, Sudhakar Kandasamy, Ng Sze
Use of Continuous Glucose Monitoring systems in the early detection and management of Cystic Fibrosis Related Diabetes in children
Akinsola Ogundiya, Marion Martin, Nancy Katkat, Laura Thomas, Joanne Russell, Sudhakar Kandasamy, Ng Sze
P2-P099
Metabolic improvement offered by Medtronic Minimed 640 G associated to transient insulin perfusion suspension before hypoglycemia in young patients with Type 1 Diabetes
Ghada AL HAGE CHEHADE, Cécile GODOT, Isabelle JOURDON, Nadine LEPAGE, Marie Eve SCHMIDT, Michel POLAK, Jacques BELTRAND
Metabolic improvement offered by Medtronic Minimed 640 G associated to transient insulin perfusion suspension before hypoglycemia in young patients with Type 1 Diabetes
Ghada AL HAGE CHEHADE, Cécile GODOT, Isabelle JOURDON, Nadine LEPAGE, Marie Eve SCHMIDT, Michel POLAK, Jacques BELTRAND
P2-P100
The glycemic variability in children with diabetes mellitus
Oleg Dianov, Ekaterina Lavrova, Sergey Gnusaev
The glycemic variability in children with diabetes mellitus
Oleg Dianov, Ekaterina Lavrova, Sergey Gnusaev
P2-P101
The levels of blood glucose and counting of carbohydrate-fat-protein in diabetic children using pump with aspart and glulisine
Esra Döğer, Rukiye Bozbulut, Şebnem Ercan, Aylin Kılınç Uğurlu, Emine Demet Akbaş, Aysun Bideci, Orhun Çamurdan, Peyami Cinaz
The levels of blood glucose and counting of carbohydrate-fat-protein in diabetic children using pump with aspart and glulisine
Esra Döğer, Rukiye Bozbulut, Şebnem Ercan, Aylin Kılınç Uğurlu, Emine Demet Akbaş, Aysun Bideci, Orhun Çamurdan, Peyami Cinaz
P2-P102
A novel missense variant, p.(Thr405Arg), in the SLC19A2 gene in an infant with thiamine responsive megaloblastic anemia syndrome presenting with anemia and diabetes but with normal hearing
Anita Spehar Uroic, Dragan Milenkovic, Ellisa De Franco, Natasa Rojnic Putarek, Nevena Krnic
A novel missense variant, p.(Thr405Arg), in the SLC19A2 gene in an infant with thiamine responsive megaloblastic anemia syndrome presenting with anemia and diabetes but with normal hearing
Anita Spehar Uroic, Dragan Milenkovic, Ellisa De Franco, Natasa Rojnic Putarek, Nevena Krnic
P2-P103
Donohue syndrome with Hypertrophic Cardiomyopathy
Derya Buluş, Esra Döğer, Dilek Sarıcı, Şeyma Kayalı, Aylin Uğurlu, Gökhan Kalkan
Donohue syndrome with Hypertrophic Cardiomyopathy
Derya Buluş, Esra Döğer, Dilek Sarıcı, Şeyma Kayalı, Aylin Uğurlu, Gökhan Kalkan
P2-P104
Age and exocrine pancreatic enzyme requirements are major determinants for carbohydrate metabolism impairment in children affected with cystic fibrosis
Janire Escudero, Amalia Uribe, José Ramón Villa, Jesús Argente, Gabriel Á. Martos-Moreno
Age and exocrine pancreatic enzyme requirements are major determinants for carbohydrate metabolism impairment in children affected with cystic fibrosis
Janire Escudero, Amalia Uribe, José Ramón Villa, Jesús Argente, Gabriel Á. Martos-Moreno
P2-P105
Post-prandial hyperinsulinaemic hypoglycaemia after oesophageal surgery in children
Antonia Dastamani, Neha Malhotra, Maria Guemes, Kate Morgan, Clare Rees, Mehul Dattani, Pratik Shah
Post-prandial hyperinsulinaemic hypoglycaemia after oesophageal surgery in children
Antonia Dastamani, Neha Malhotra, Maria Guemes, Kate Morgan, Clare Rees, Mehul Dattani, Pratik Shah
P2-P106
Congenital Hyperinsulinism: clinical and molecular characteristics – Fluorine-18-L-dihydroxyphenylalanine positron emission tomography (F-DOPA PET) scan results -treatment responses and short term outcomes of 5 patients
Hande Turan, Aydilek Dagdeviren Cakir, Atilla Cayir, Elisa De Franco, Sian Ellard, Kerim Sönmezoglu, Oya Ercan, Saadet Olcay Evliyaoglu
Congenital Hyperinsulinism: clinical and molecular characteristics – Fluorine-18-L-dihydroxyphenylalanine positron emission tomography (F-DOPA PET) scan results -treatment responses and short term outcomes of 5 patients
Hande Turan, Aydilek Dagdeviren Cakir, Atilla Cayir, Elisa De Franco, Sian Ellard, Kerim Sönmezoglu, Oya Ercan, Saadet Olcay Evliyaoglu
P2-P107
Congenital Hyperinsulinism in a child with Alagille Syndrome
Durray Shahwar Khan, Antonia Dastamani, Hannah Antell, Pratik Shah
Congenital Hyperinsulinism in a child with Alagille Syndrome
Durray Shahwar Khan, Antonia Dastamani, Hannah Antell, Pratik Shah
P2-P108
Severe stress-induced subcutaneous and intravenous insulin resistance in an eight year old boy with T1DM, necessitating seven months of IV insulin, reversed after psychiatric treatment.
C.C.N. van Ommen, J.J.G. Hoorweg-Nijman, H. Stuart, P.K.H. Deschamps, A.A. Verrijn Stuart
Severe stress-induced subcutaneous and intravenous insulin resistance in an eight year old boy with T1DM, necessitating seven months of IV insulin, reversed after psychiatric treatment.
C.C.N. van Ommen, J.J.G. Hoorweg-Nijman, H. Stuart, P.K.H. Deschamps, A.A. Verrijn Stuart
P2-P109
A case of neonatal diabetes due to pancreatic hypoplasia
Zacharoula Karabouta, Maria Katsafiloudi, Vasiliki Bisbinas, Margarita Karametou, Chrisa Karali, Andreas Giannopoulos
A case of neonatal diabetes due to pancreatic hypoplasia
Zacharoula Karabouta, Maria Katsafiloudi, Vasiliki Bisbinas, Margarita Karametou, Chrisa Karali, Andreas Giannopoulos
P2-P110
Neonatal Diabetes Mellitus caused by a novel GLIS3 mutation in twins
Shira London, Ghadir Elias-Assad, Marie Noufi Barhoum, Clari Felszer, Marina Paniakov, Scott Vainer, Sarah Flanagan, Jayne Houghton, Yardena Tenenbaum Rakover
Neonatal Diabetes Mellitus caused by a novel GLIS3 mutation in twins
Shira London, Ghadir Elias-Assad, Marie Noufi Barhoum, Clari Felszer, Marina Paniakov, Scott Vainer, Sarah Flanagan, Jayne Houghton, Yardena Tenenbaum Rakover
P2-P111
Permanent Neonatal Diabetes, Hepatic Failure and Progressive Left Hemispheric Cerebral Atrophy in a patient with Wolcott-Rallison Syndrome:a clinical and genetic study from the state of Qatar
Sara Al-Khawaga, Reem Hasnah, Saras Saraswathi, Ahmed Elawa, Khalid Hussain*
Permanent Neonatal Diabetes, Hepatic Failure and Progressive Left Hemispheric Cerebral Atrophy in a patient with Wolcott-Rallison Syndrome:a clinical and genetic study from the state of Qatar
Sara Al-Khawaga, Reem Hasnah, Saras Saraswathi, Ahmed Elawa, Khalid Hussain*
P2-P112
A RARE CASE OF DIABETES MELLITUS TYPE 1 IN A CHILD WITH NEUROFIBROMATOSIS TYPE 1
Eleni Panoutsou, Maria-Zoi Oikonomakou, Markella Vallianatou, Eleni Koufoglou, Sotiria Giannopoulou, Maria Eliopoulou
A RARE CASE OF DIABETES MELLITUS TYPE 1 IN A CHILD WITH NEUROFIBROMATOSIS TYPE 1
Eleni Panoutsou, Maria-Zoi Oikonomakou, Markella Vallianatou, Eleni Koufoglou, Sotiria Giannopoulou, Maria Eliopoulou
P2-P113
Detection and analysis of glycometabolism related genes in children diabetes
Lin QI Chen, Xiao Yan Wang, Hai Ying Wu, Ting Chen, Xiu LI Chen, Hui Sun, Feng Yun Wang
Detection and analysis of glycometabolism related genes in children diabetes
Lin QI Chen, Xiao Yan Wang, Hai Ying Wu, Ting Chen, Xiu LI Chen, Hui Sun, Feng Yun Wang
P2-P114
Gender characteristics of responsibility for their own health of adolescents with Type I Diabetes Mellitus
Olena Kyrylova, Olena Budreiko, Svitlana Chumak
Gender characteristics of responsibility for their own health of adolescents with Type I Diabetes Mellitus
Olena Kyrylova, Olena Budreiko, Svitlana Chumak
P2-P115
Favorable outcome despite prolonged hypoglycemic episodes following a massive insulin overdose: a case series
Heike Vollbach, Bettina Gohlke, Sandra Schulte, Joachim Woelfle
Favorable outcome despite prolonged hypoglycemic episodes following a massive insulin overdose: a case series
Heike Vollbach, Bettina Gohlke, Sandra Schulte, Joachim Woelfle
P2-P116
Effect of a reduced fluid replacement regimen on the resolution of diabetic ketoacidosis (DKA) in children
Danica Shanee Hapuarachchi, Jaberuzzaman Ahmed, Evelien Gevers, Abdul Moodambail, Ajay Thankamony
Effect of a reduced fluid replacement regimen on the resolution of diabetic ketoacidosis (DKA) in children
Danica Shanee Hapuarachchi, Jaberuzzaman Ahmed, Evelien Gevers, Abdul Moodambail, Ajay Thankamony
P2-P117
Prevalence of and risk factors for nonadherence to insulin among paediatric Type 1 Diabetes patients in Singapore
Brandon Chua, Jamie Stephanie, XIn Yan Lim, Kar Men Poh, McVin Cheen, Soo Ting Lim, Ngee Lek
Prevalence of and risk factors for nonadherence to insulin among paediatric Type 1 Diabetes patients in Singapore
Brandon Chua, Jamie Stephanie, XIn Yan Lim, Kar Men Poh, McVin Cheen, Soo Ting Lim, Ngee Lek
P2-P118
"What do you know about your diabetes?”: a qualitative and quantitative study of teenagers and young adults’ understanding of their disease
Jehanne Malek, Cécile Petit-Bibal, Elsa Denis, Juliette Eroukhmanoff, Gianpaolo De Filippo
"What do you know about your diabetes?”: a qualitative and quantitative study of teenagers and young adults’ understanding of their disease
Jehanne Malek, Cécile Petit-Bibal, Elsa Denis, Juliette Eroukhmanoff, Gianpaolo De Filippo
P2-P119
Parental knowledge and attitudes toward Diabetes Mellitus Type 1: a cross sectional study
Norah Albanyan, Abdulhameed Albanyan, Ahmad Adel, Mohammed Zaiton
Parental knowledge and attitudes toward Diabetes Mellitus Type 1: a cross sectional study
Norah Albanyan, Abdulhameed Albanyan, Ahmad Adel, Mohammed Zaiton
P2-P120
Identifying the association of depression and diabetic distress in Pakistani patients diagnosed with type 1 diabetes
Arooj Fatima, Syed Sammar Abbas Zaidi
Identifying the association of depression and diabetic distress in Pakistani patients diagnosed with type 1 diabetes
Arooj Fatima, Syed Sammar Abbas Zaidi
P2-P121
ROLE OF BREASTFEEDING IN PREVENTION OF TYPE 1 DIABETES in Pakistan.
Arooj Fatima, Syed Sammar Abbas Zaidi
ROLE OF BREASTFEEDING IN PREVENTION OF TYPE 1 DIABETES in Pakistan.
Arooj Fatima, Syed Sammar Abbas Zaidi
P2-P122
A young Type 1 Diabetic with Acute Hemichorea: rare central nervous system complications
Andrew Sng, Jeremy Lin, Amanda Zain, Yvonne Lim
A young Type 1 Diabetic with Acute Hemichorea: rare central nervous system complications
Andrew Sng, Jeremy Lin, Amanda Zain, Yvonne Lim
P3-P071
Multiple autoimmune association and varied spectrum of presentation in Indian diabetic children
Aashish Sethi, Smita Ramachandran, Inderpal Kochar
Multiple autoimmune association and varied spectrum of presentation in Indian diabetic children
Aashish Sethi, Smita Ramachandran, Inderpal Kochar
P3-P072
Severe Hypertriglyceridemia and Multiple Autoimmune Phenomenon at new onset Type 1 DM
Aashish Sethi, Smita Ramachandran, Inderpal Kochar
Severe Hypertriglyceridemia and Multiple Autoimmune Phenomenon at new onset Type 1 DM
Aashish Sethi, Smita Ramachandran, Inderpal Kochar
P3-P074
Association between prior Toxic Stressors and development of T2DM in adolescents
Adam Adamidis, MD, Alexander Knee, MS, Victoria Cobb, BS, Rushika Conroy, MD MS
Association between prior Toxic Stressors and development of T2DM in adolescents
Adam Adamidis, MD, Alexander Knee, MS, Victoria Cobb, BS, Rushika Conroy, MD MS
P3-P075
First 4 cases of neonatal diabetes from Kazakhstan, Almaty with proven mutations in KCNJ11 and INS genes
Akmaral Nurbekova, Andrew Hattersley, Svetlana Ten, Amrit Bhangoo
First 4 cases of neonatal diabetes from Kazakhstan, Almaty with proven mutations in KCNJ11 and INS genes
Akmaral Nurbekova, Andrew Hattersley, Svetlana Ten, Amrit Bhangoo
P3-P076
First 2 cases of monogenic diabetes (MODY) from Kazakhstan, Almaty with proven heterozygous mutation in hepatocyte nuclear factor 1-alpha (HNF1A) gene
Akmaral Nurbekova, Andrew Hattersley, Svetlana Ten, Amrit Bhangoo
First 2 cases of monogenic diabetes (MODY) from Kazakhstan, Almaty with proven heterozygous mutation in hepatocyte nuclear factor 1-alpha (HNF1A) gene
Akmaral Nurbekova, Andrew Hattersley, Svetlana Ten, Amrit Bhangoo
P3-P077
Achievement of therapy targets in children and adolescents with Type 1 Diabetes mellitus at the “Diabetes School”
Akmaral Tashmanova, Laura Danyarova, Gulnara Rakhimova
Achievement of therapy targets in children and adolescents with Type 1 Diabetes mellitus at the “Diabetes School”
Akmaral Tashmanova, Laura Danyarova, Gulnara Rakhimova
P3-P078
Characteristics of MODY-GCK diabetes in children and adolescents in Siberia
Alla Ovsyannikova, Oksana Rymar, Elena Shakhtshneider, Dinara Ivanoshchuk
Characteristics of MODY-GCK diabetes in children and adolescents in Siberia
Alla Ovsyannikova, Oksana Rymar, Elena Shakhtshneider, Dinara Ivanoshchuk
P3-P079
Clinical case of MODY-GCK diabetes: heterogeneity of course among relatives from one family
Alla Ovsyannikova, Oksana Rymar, Elena Shakhtshneider, Dinara Ivanoshchuk, Mikhail Voevoda
Clinical case of MODY-GCK diabetes: heterogeneity of course among relatives from one family
Alla Ovsyannikova, Oksana Rymar, Elena Shakhtshneider, Dinara Ivanoshchuk, Mikhail Voevoda
P3-P080
Clinical and biochemical characteristics of Familial Type 1 Diabetes Mellitus (FT1DM) compared to Non-Familial Type 1 DM (T1DM)
Fawzia Alyafei, Ashraf Soliman, Fawziya Alkhalaf, Amal Sabt, Reem Waseef, Nagwa Eldarsy, Anas Abdulkayoum, Fareeda Umer
Clinical and biochemical characteristics of Familial Type 1 Diabetes Mellitus (FT1DM) compared to Non-Familial Type 1 DM (T1DM)
Fawzia Alyafei, Ashraf Soliman, Fawziya Alkhalaf, Amal Sabt, Reem Waseef, Nagwa Eldarsy, Anas Abdulkayoum, Fareeda Umer
P3-P081
Prevalence of beta-cell antibodies and associated autoimmune diseases in children and adolescents with Type 1 (T1DM) versus Type 2 Diabetes Mellitus (T2DM) in Qatar
Fawzia Alyafei, Ashraf Soliman, Fawziya Alkhalaf, Aml Sabt, Reem Waseef, Nagwa Eldarsy, Mona Algamal
Prevalence of beta-cell antibodies and associated autoimmune diseases in children and adolescents with Type 1 (T1DM) versus Type 2 Diabetes Mellitus (T2DM) in Qatar
Fawzia Alyafei, Ashraf Soliman, Fawziya Alkhalaf, Aml Sabt, Reem Waseef, Nagwa Eldarsy, Mona Algamal
P3-P082
Clinical presentation and autoimmune markers in children and adolescents with Familial Type 1 Diabetes Mellitus (FT1DM) and Familial Type 2 Diabetes Mellitus (FT2DM)
Fawzia Alyafei, Ashraf Soliman, Fawziya Alkhalaf, Amal Sabt, Reem Waseef, Nagwa Aldarsy, Mona Algamal
Clinical presentation and autoimmune markers in children and adolescents with Familial Type 1 Diabetes Mellitus (FT1DM) and Familial Type 2 Diabetes Mellitus (FT2DM)
Fawzia Alyafei, Ashraf Soliman, Fawziya Alkhalaf, Amal Sabt, Reem Waseef, Nagwa Aldarsy, Mona Algamal
P3-P083
Real–world clinical evolution of Type 1 Diabetes patients on twenty years
Amparo Gonzalez Vergaz, Beatriz Garcia Cuartero, Laura Sanchez Salado, Veronica Sanchez Escudero, Concepción García Lacalle, Marta Fernández Férnandez
Real–world clinical evolution of Type 1 Diabetes patients on twenty years
Amparo Gonzalez Vergaz, Beatriz Garcia Cuartero, Laura Sanchez Salado, Veronica Sanchez Escudero, Concepción García Lacalle, Marta Fernández Férnandez
P3-P084
Diabetic capilaropathy: a case report
Carlos Andrés, Laura Tabuenca, Idoia Sanchez, Laura Diaz, Maria J. Chueca, Sara Berrade, Teodoro Dura, Esther Compains
Diabetic capilaropathy: a case report
Carlos Andrés, Laura Tabuenca, Idoia Sanchez, Laura Diaz, Maria J. Chueca, Sara Berrade, Teodoro Dura, Esther Compains
P3-P085
A sibling case of Wolfram syndrome with diabetes mellitus diagnosed within 10 months in early childhood
Dai Suzuki, Hirohito Shima, Ikumi Umeki, Miki Kamimura, Junko Kanno, Shigeo Kure, Ikuma Fujiwara
A sibling case of Wolfram syndrome with diabetes mellitus diagnosed within 10 months in early childhood
Dai Suzuki, Hirohito Shima, Ikumi Umeki, Miki Kamimura, Junko Kanno, Shigeo Kure, Ikuma Fujiwara
P3-P086
Continuous subcutaneous insulin infusion in children and adolescents: analysis of initial and follow up basal rates
Gunay Demir, Sukran Darcan, Samim Özen, Hafize Işıklar, Yasemin Atik Altınok, Damla Goksen
Continuous subcutaneous insulin infusion in children and adolescents: analysis of initial and follow up basal rates
Gunay Demir, Sukran Darcan, Samim Özen, Hafize Işıklar, Yasemin Atik Altınok, Damla Goksen
P3-P087
Prevalance of fatty liver in patients with Type 1 Diabetes Mellitus attending diabetes clinic at Alexandria University Children's Hospital
Dina fawzy, Shaymaa elsayed, Mahmoud Adel abdel-moneim
Prevalance of fatty liver in patients with Type 1 Diabetes Mellitus attending diabetes clinic at Alexandria University Children's Hospital
Dina fawzy, Shaymaa elsayed, Mahmoud Adel abdel-moneim
P3-P088
THE TRIAD OF OBESITY, ACANTHOSIS NIGRICANS AND DIABETES MELLITUS IN A NEWLY DIAGNOSED ADOLESCENT; IS THIS TYPE 1 OR TYPE 2 DIABETES MELLITUS?
Dipesalema Joel, Tshireletso Ramaphane, Motlalekgomo Matsheng-Samuel, Seeletso Nchingane
THE TRIAD OF OBESITY, ACANTHOSIS NIGRICANS AND DIABETES MELLITUS IN A NEWLY DIAGNOSED ADOLESCENT; IS THIS TYPE 1 OR TYPE 2 DIABETES MELLITUS?
Dipesalema Joel, Tshireletso Ramaphane, Motlalekgomo Matsheng-Samuel, Seeletso Nchingane
P3-P090
Clinical and laboratory features at the onset of childhood type 1 diabetes mellitus in the Nortwest region (Trakya) of Turkey
Emine Dilek, Digdem Bezen, Fatma Ozguc Comlek, Beyhan Ozkaya, Filiz Tutunculer
Clinical and laboratory features at the onset of childhood type 1 diabetes mellitus in the Nortwest region (Trakya) of Turkey
Emine Dilek, Digdem Bezen, Fatma Ozguc Comlek, Beyhan Ozkaya, Filiz Tutunculer
P3-P091
Clinical and epidemiological features of children with Type 1 Diabetes
Şule Demir, Peyami Cinaz, Esra Döğer, Aylin Kılınç Uğurlu, Emine Demet Akbaş, Aysun Bideci, Orhun Çamurdan
Clinical and epidemiological features of children with Type 1 Diabetes
Şule Demir, Peyami Cinaz, Esra Döğer, Aylin Kılınç Uğurlu, Emine Demet Akbaş, Aysun Bideci, Orhun Çamurdan
P3-P092
Predictors of Optimal Glycemic Control in Children with Diabetes Mellitus Type 1 Receiving Pump Insulin Therapy.
Evgeniya Evsyukova, Irina Kolomina, Sergey Bukin, Elena Kiseleva, Oleg Latyshev, Goar Okminyan, Lyubov Samsonova
Predictors of Optimal Glycemic Control in Children with Diabetes Mellitus Type 1 Receiving Pump Insulin Therapy.
Evgeniya Evsyukova, Irina Kolomina, Sergey Bukin, Elena Kiseleva, Oleg Latyshev, Goar Okminyan, Lyubov Samsonova
P3-P093
Symptomatic cerebral infarction:a rare complication of diabetic ketoacidosis
Gamze Celmeli, Mesut Parlak, Sema Akcurin, Iffet Bircan
Symptomatic cerebral infarction:a rare complication of diabetic ketoacidosis
Gamze Celmeli, Mesut Parlak, Sema Akcurin, Iffet Bircan
P3-P094
OUR CLINICAL EXPERIENCES IN TYPE 2 DIABETES
gül direk, Zeynep Uzan Tatlı, Merve Nur Hepokur, Ülkü Gül Şiraz, Leyla Akın, Nihal Hatipoğlu, Mustafa Kendirci, Selim Kurtoğlu
OUR CLINICAL EXPERIENCES IN TYPE 2 DIABETES
gül direk, Zeynep Uzan Tatlı, Merve Nur Hepokur, Ülkü Gül Şiraz, Leyla Akın, Nihal Hatipoğlu, Mustafa Kendirci, Selim Kurtoğlu
P3-P095
The relationship between serum levels of C-peptide and the age, body mass index, and insülin doses in newly diagnosed Type 1 diabetic children
Gülay Karagüzel, Deniz Usta, Ayşegül Tavaci, Mustafa Taniş, Ercüment Beyhun
The relationship between serum levels of C-peptide and the age, body mass index, and insülin doses in newly diagnosed Type 1 diabetic children
Gülay Karagüzel, Deniz Usta, Ayşegül Tavaci, Mustafa Taniş, Ercüment Beyhun
P3-P096
Serum trace element levels in children presenting with diabetic ketozis and diabetic ketoacidosis: a longitudinal controlled study
Hakan Doneray, Kadri Gurbuz, Ayse Ozden, Mehmet Ali Gul, Zerrin Orbak
Serum trace element levels in children presenting with diabetic ketozis and diabetic ketoacidosis: a longitudinal controlled study
Hakan Doneray, Kadri Gurbuz, Ayse Ozden, Mehmet Ali Gul, Zerrin Orbak
P3-P097
Evaluation of relation between diabetic education levels of Type 1 DM child/adolescent and parents and metabolic control
Havva Nur Peltek Kendirci, Ümran Karayurt, Emre Demir
Evaluation of relation between diabetic education levels of Type 1 DM child/adolescent and parents and metabolic control
Havva Nur Peltek Kendirci, Ümran Karayurt, Emre Demir
P3-P098
A CASE OF CHILDHOOD TYPE 1 DIABETES MELLITUS WHO DEVELOPED GRANULOMA ANNULARE
Aynure Öztekin, Havva Nur Peltek Kendirci, Güven Güney
A CASE OF CHILDHOOD TYPE 1 DIABETES MELLITUS WHO DEVELOPED GRANULOMA ANNULARE
Aynure Öztekin, Havva Nur Peltek Kendirci, Güven Güney
P3-P099
Case report: De Novo mutation of FOXP3 causing mild phenotype of immunodysregulation, polyendocrinopathy, enteropathy, X-link Syndrome
HOANG THI DIEM THUY, NGUYEN KHOA BINH MINH
Case report: De Novo mutation of FOXP3 causing mild phenotype of immunodysregulation, polyendocrinopathy, enteropathy, X-link Syndrome
HOANG THI DIEM THUY, NGUYEN KHOA BINH MINH
P3-P100
Is there a relationship between Immune-mediated Type 1 Diabetes Mellitus and Congenital Rubella infection?
Huseyin Anil Korkmaz, Çağatay Ermis
Is there a relationship between Immune-mediated Type 1 Diabetes Mellitus and Congenital Rubella infection?
Huseyin Anil Korkmaz, Çağatay Ermis
P3-P101
Changes in glycemic control after switching from NPH & RI to Insulin Glargine & Lispro in children with Type 1 Diabetes Mellitus (T1DM)
Hyeon-A Kim, Jung-Eun Moon, Soo-Jeong Lee, Gi-Min Lee, Cheol-Woo Ko
Changes in glycemic control after switching from NPH & RI to Insulin Glargine & Lispro in children with Type 1 Diabetes Mellitus (T1DM)
Hyeon-A Kim, Jung-Eun Moon, Soo-Jeong Lee, Gi-Min Lee, Cheol-Woo Ko
P3-P102
When Type Mody II Diabetes simulates Type I Diabetes
IRENE PILAR FERNANDEZ VISERAS, MARIA ANGELES SANTOS MATA, ISABEL TORRES BAREA, LUIS CASTAÑO GONZALEZ
When Type Mody II Diabetes simulates Type I Diabetes
IRENE PILAR FERNANDEZ VISERAS, MARIA ANGELES SANTOS MATA, ISABEL TORRES BAREA, LUIS CASTAÑO GONZALEZ
P3-P103
Epidemiological study and analysis of Type 1 Diabetes comparing patients with and without Ketoacidosis in the last 5 years
IRENE PILAR FERNANDEZ VISERAS, MARIA ANGELES SANTOS MATA, SILVIA PONCE DELGADO, CELIA MORALES PEREZ, FRANCISCO JOSE MACIAS LOPEZ
Epidemiological study and analysis of Type 1 Diabetes comparing patients with and without Ketoacidosis in the last 5 years
IRENE PILAR FERNANDEZ VISERAS, MARIA ANGELES SANTOS MATA, SILVIA PONCE DELGADO, CELIA MORALES PEREZ, FRANCISCO JOSE MACIAS LOPEZ
P3-P104
The frequency of diabetic ketoacidosis hospitalization in Siberian children and adolescent
Irina Osokina
The frequency of diabetic ketoacidosis hospitalization in Siberian children and adolescent
Irina Osokina
P3-P105
Monogenic Diabetes cause by mutation of the gene HNF–1A
JUAN MANUEL NARVAEZ, MARIA CLEMENTE LEON, JOSEP ORIOL
Monogenic Diabetes cause by mutation of the gene HNF–1A
JUAN MANUEL NARVAEZ, MARIA CLEMENTE LEON, JOSEP ORIOL
P3-P106
Reversibility of early acute Diabetic Neuropathy (DN) in adolescents with Type 1 Diabetes Mellitus (T1D)
Maria Louraki, Panagiotis Kokotis, Marina Katsalouli, Dimitra Kallinikou, Christina Kanaka-Gantenbein, Kyriaki Karavanaki
Reversibility of early acute Diabetic Neuropathy (DN) in adolescents with Type 1 Diabetes Mellitus (T1D)
Maria Louraki, Panagiotis Kokotis, Marina Katsalouli, Dimitra Kallinikou, Christina Kanaka-Gantenbein, Kyriaki Karavanaki
P3-P107
The value of continuous hemodiafiltration in rescuing children with severe diabetic ketoacidosis
Lin QI Chen, Dan Dan Zhang, Hai Ying Wu, Ting Chen, Xiu Li Chen, Feng Yun Wang, Rong Rong Xie
The value of continuous hemodiafiltration in rescuing children with severe diabetic ketoacidosis
Lin QI Chen, Dan Dan Zhang, Hai Ying Wu, Ting Chen, Xiu Li Chen, Feng Yun Wang, Rong Rong Xie
P3-P108
Psychosocial risks, comorbidities and health events during the follow-up of children and adolescents with Type 1 Diabetes
Mª Carmen Temboury, Raquel Villamor, Mª Belen Hernandez, Sara Lapeña, Cristina Lopez
Psychosocial risks, comorbidities and health events during the follow-up of children and adolescents with Type 1 Diabetes
Mª Carmen Temboury, Raquel Villamor, Mª Belen Hernandez, Sara Lapeña, Cristina Lopez
P3-P109
Clinical profile and outcome of Diabetic Ketoacidosis in a tertiary care teaching hospital of a developing country
Meghna Chawla, Tushar Deshpande, M.K. Behera
Clinical profile and outcome of Diabetic Ketoacidosis in a tertiary care teaching hospital of a developing country
Meghna Chawla, Tushar Deshpande, M.K. Behera
P3-P110
Diabetes Mellitus, Autoimmune Hemolytic Anemia, Hepatosplenomegaly and Lymphadenopathy: a rare association in Chinese children
Miaoying Zhang, Xiaojing Li, Li Xi, Zhuhui Zhao, Ruoqian Cheng, Bingbing Wu, Feihong Luo
Diabetes Mellitus, Autoimmune Hemolytic Anemia, Hepatosplenomegaly and Lymphadenopathy: a rare association in Chinese children
Miaoying Zhang, Xiaojing Li, Li Xi, Zhuhui Zhao, Ruoqian Cheng, Bingbing Wu, Feihong Luo
P3-P111
Type 1 diabetes and central precocious puberty a rare association
mimouna bessahraoui, nassima oussaleh, sidi mohamed azzouz, radia rezak
Type 1 diabetes and central precocious puberty a rare association
mimouna bessahraoui, nassima oussaleh, sidi mohamed azzouz, radia rezak
P3-P112
DIABETIC KETOACIDOSIS AMONG EGYPTIAN CHILDREN WITH TYPE 1 DIABETES: 3-YEARS STUDY
Mona Karem, Khalid Alsabahy, Ahmed Elfiky, Ahmed Meshref, Heba Akl
DIABETIC KETOACIDOSIS AMONG EGYPTIAN CHILDREN WITH TYPE 1 DIABETES: 3-YEARS STUDY
Mona Karem, Khalid Alsabahy, Ahmed Elfiky, Ahmed Meshref, Heba Akl
P3-P113
Fructosamine level in Type 1 Diabetes Mellitus children performing Ramadhan fasting
muhammad faizi, Nur Rochmah
Fructosamine level in Type 1 Diabetes Mellitus children performing Ramadhan fasting
muhammad faizi, Nur Rochmah
P3-P114
Metformin therapy ina lean adolescent girl with prediabetes dysglycemia treated: good response
Nada AlAaraj, Amene Hermi, Noor Hamed, Shaymaa Ahmed, Ashraf Soliman
Metformin therapy ina lean adolescent girl with prediabetes dysglycemia treated: good response
Nada AlAaraj, Amene Hermi, Noor Hamed, Shaymaa Ahmed, Ashraf Soliman
P3-P115
Association between Thyroid Stimulating Hormone and Hemoglobine A1c in Type 1 Diabetes Mellitus children
nur rochmah, Muhammad Faizi
Association between Thyroid Stimulating Hormone and Hemoglobine A1c in Type 1 Diabetes Mellitus children
nur rochmah, Muhammad Faizi
P3-P116
Monogenic Diabetes in 2 years and 4 monthsold girl: is it DEND?
Nur Rochmah, Muhammad Faizi, Arie Purwana
Monogenic Diabetes in 2 years and 4 monthsold girl: is it DEND?
Nur Rochmah, Muhammad Faizi, Arie Purwana
P3-P117
Compliance for monitoring of glycemic control in children with Type 1 Diabetes
Oleg Latyshev, Maria Simakova, Lyubov Samsonova, Goar Okminyan, Elena Kiseleva, Alexander Fialtov, Elvira Kasatkina
Compliance for monitoring of glycemic control in children with Type 1 Diabetes
Oleg Latyshev, Maria Simakova, Lyubov Samsonova, Goar Okminyan, Elena Kiseleva, Alexander Fialtov, Elvira Kasatkina
P3-P118
Ketogenic diet in a child with diabetes and global developmental delay
Myat Win, Usha Rajalingam, Rajiv Goonetilleke
Ketogenic diet in a child with diabetes and global developmental delay
Myat Win, Usha Rajalingam, Rajiv Goonetilleke
P3-P119
A rare cause of severe anemia in a patient with type 1 diabetes
Robert Piekarski, Anna Bury, Iwona Beń-Skowronek
A rare cause of severe anemia in a patient with type 1 diabetes
Robert Piekarski, Anna Bury, Iwona Beń-Skowronek
P3-P120
Oral Gliclazide (A Sulfonylurea) Monotherapy is effective and safe in the management of T2DM in children:a case report
Shayma Ahmed, Ashraf Soliman, Nada Alaaraj, Noor Hamad
Oral Gliclazide (A Sulfonylurea) Monotherapy is effective and safe in the management of T2DM in children:a case report
Shayma Ahmed, Ashraf Soliman, Nada Alaaraj, Noor Hamad
P3-P121
Pediatric stroke as the presenting symptom of new onset diabetes without DKA
Sonum Bharill, Cathrine Constantacos
Pediatric stroke as the presenting symptom of new onset diabetes without DKA
Sonum Bharill, Cathrine Constantacos
P3-P122
Challenges In Educating New Onset Type 1 Diabetes MellitusPatients: Can The Use Of a Tablet Be The Answer?
Javier Aisenberg, Lynda Rosini, Jeanette Haugh, Susan Mathus, Michele De Vito, Ingrid Brennan, Steven Ghanny
Challenges In Educating New Onset Type 1 Diabetes MellitusPatients: Can The Use Of a Tablet Be The Answer?
Javier Aisenberg, Lynda Rosini, Jeanette Haugh, Susan Mathus, Michele De Vito, Ingrid Brennan, Steven Ghanny
P3-P123
AID-GM system (Advanced Intelligent Distant – Glucose Monitoring) to monitor health status and metabolic control of young people with type 1 diabetes
Valeria Calcaterra, Lucia Sacchi, Elisa Salvi, Daniela Larizza, Alexandra Madé, Luca Maria Schiano, Chiara Montalbano, Corrado Regalbuto, Riccardo Bellazzi, Cristiana Larizza
AID-GM system (Advanced Intelligent Distant – Glucose Monitoring) to monitor health status and metabolic control of young people with type 1 diabetes
Valeria Calcaterra, Lucia Sacchi, Elisa Salvi, Daniela Larizza, Alexandra Madé, Luca Maria Schiano, Chiara Montalbano, Corrado Regalbuto, Riccardo Bellazzi, Cristiana Larizza
P3-P124
Continuous glucose monitoring results of our cases with MODY type 2 diabetes
zeynep uzan tatlı, gul direk, mervenur hepokur, nihal hatipoğlu, leyla akın, mustafa kendirci, selim kurtoglu
Continuous glucose monitoring results of our cases with MODY type 2 diabetes
zeynep uzan tatlı, gul direk, mervenur hepokur, nihal hatipoğlu, leyla akın, mustafa kendirci, selim kurtoglu
P3-P399
Family Investigation and Clinical Phenotype Analysis of Type A Insulin Resistance Syndrome
Yonghua Chen, hong chen, yanlan fang, chunlin wang, jianfang zhu, li liang
Family Investigation and Clinical Phenotype Analysis of Type A Insulin Resistance Syndrome
Yonghua Chen, hong chen, yanlan fang, chunlin wang, jianfang zhu, li liang
P3-P403
Epidemiology, Demographic Criteria and Risk Factors in Type 1 DM Egyptian Children; A Single Center Study
Nora Badawi, Yomna Shaalan
Epidemiology, Demographic Criteria and Risk Factors in Type 1 DM Egyptian Children; A Single Center Study
Nora Badawi, Yomna Shaalan
P3-P407
DEGLUDEC VERSUS GLARGINE IN PEDIATRIC AND ADOLESCENT PATIENTS WITH TYPE 1 DIABETES
Estela Gil-Poch, Francisco Javier Arroyo-Díez, Pilar I Beato-Víbora
DEGLUDEC VERSUS GLARGINE IN PEDIATRIC AND ADOLESCENT PATIENTS WITH TYPE 1 DIABETES
Estela Gil-Poch, Francisco Javier Arroyo-Díez, Pilar I Beato-Víbora
P3-P416
A rare and unexpected cause of diabetes in childhood
Taffy Makaya, Supriyo Basu, Aishatu Ali
A rare and unexpected cause of diabetes in childhood
Taffy Makaya, Supriyo Basu, Aishatu Ali
P3-P417
STUDY OF CHILDREN WITH TYPE 1 DIABETES MELLITUS OF LONG DURATION ATTENDING ALEXANDRIA UNIVERSITY CHILDREN'S HOSPITAL
Dina fawzy, Shaymaa Elsayed, Mahmoud Abd el-moneim
STUDY OF CHILDREN WITH TYPE 1 DIABETES MELLITUS OF LONG DURATION ATTENDING ALEXANDRIA UNIVERSITY CHILDREN'S HOSPITAL
Dina fawzy, Shaymaa Elsayed, Mahmoud Abd el-moneim
RFC12.1
Use of acid-suppressivemedications during infancy and early childhood and its association with type 1 diabetes
Sruthi Menon, Krishna Kishore Umapathi, Aravind Thavaman, Geetanjali Bora, Ajuah Davis
Use of acid-suppressivemedications during infancy and early childhood and its association with type 1 diabetes
Sruthi Menon, Krishna Kishore Umapathi, Aravind Thavaman, Geetanjali Bora, Ajuah Davis
RFC12.2
Bone mineral density is increased in 276 Danish children and adolescents with Type-1-Diabetes.
Jens Otto Broby Madsen, Camilla Winther Herskin, Bo Zerahn, Birthe Susanne Olsen, Flemming Pociot, Jesper Johannesen
Bone mineral density is increased in 276 Danish children and adolescents with Type-1-Diabetes.
Jens Otto Broby Madsen, Camilla Winther Herskin, Bo Zerahn, Birthe Susanne Olsen, Flemming Pociot, Jesper Johannesen
RFC12.3
Barriers and sources of support for the performance of physical activity in pediatric Type 1 Diabetes
Ruth Livny, Wasim Said, Smadar Shilo, Shoshana Gal, Meirav Oren, Ram Weiss, Nehama Zuckerman-Levin, Naim Shehadeh, Michal Cohen
Barriers and sources of support for the performance of physical activity in pediatric Type 1 Diabetes
Ruth Livny, Wasim Said, Smadar Shilo, Shoshana Gal, Meirav Oren, Ram Weiss, Nehama Zuckerman-Levin, Naim Shehadeh, Michal Cohen
RFC12.4
Use of telemonitoring via a mobile device app reduces HbA1c in type 1 diabetic children and adolescents
Philippe Klee, Catherine Bussien, Montserrat Castellsague, Christophe Combescure, Mirjam Dirlewanger, Céline Girardin, Jean-Luc Mando, Luz Perrenoud, Carole Salomon, Franck Schneider, Valérie Schwitzgebel
Use of telemonitoring via a mobile device app reduces HbA1c in type 1 diabetic children and adolescents
Philippe Klee, Catherine Bussien, Montserrat Castellsague, Christophe Combescure, Mirjam Dirlewanger, Céline Girardin, Jean-Luc Mando, Luz Perrenoud, Carole Salomon, Franck Schneider, Valérie Schwitzgebel
RFC12.5
Insulin gene promoter methylation status in Greek children and adolescents with Type 1 Diabetes
Konstantina Mouzaki, Eleni P Kotanidou, Aikaterini Fragou, Styliani Giza, Angeliki N Kleisarchaki, Vasiliki Rengina Tsinopoulou, Anastasios Serbis, Georgios Tzimagiorgis, Assimina Galli-Tsinopoulou
Insulin gene promoter methylation status in Greek children and adolescents with Type 1 Diabetes
Konstantina Mouzaki, Eleni P Kotanidou, Aikaterini Fragou, Styliani Giza, Angeliki N Kleisarchaki, Vasiliki Rengina Tsinopoulou, Anastasios Serbis, Georgios Tzimagiorgis, Assimina Galli-Tsinopoulou
RFC12.6
AMGLIDIA, a suspension of glibenclamide for patients with neonatal diabetes, long term data on efficiency and tolerance
jacques beltrand, Candice meyzer, sandra colas, michaela semeraro, cécile godot, jean-marc treluyer, caroline elie, michel polak
AMGLIDIA, a suspension of glibenclamide for patients with neonatal diabetes, long term data on efficiency and tolerance
jacques beltrand, Candice meyzer, sandra colas, michaela semeraro, cécile godot, jean-marc treluyer, caroline elie, michel polak
RFC3.1
Diagnostics of early atherosclerosis risk in Kids (DEAR-Kids): retinal vessel analysis in pediatric Type 1 Diabetes – retinal arteriolar narrowing caused by high HbA1c
Michael Wurm, Kühnemund Leonie, Lisa Maier, Xia Mi, Kai Lichte, Kristiane Hallermann, Alexandra Krause, Corinna Brichta, Natascha van der Werf-Grohmann, Andreas Krebs, Henner Hanssen, Peter Deibert, Karl Otfried Schwab
Diagnostics of early atherosclerosis risk in Kids (DEAR-Kids): retinal vessel analysis in pediatric Type 1 Diabetes – retinal arteriolar narrowing caused by high HbA1c
Michael Wurm, Kühnemund Leonie, Lisa Maier, Xia Mi, Kai Lichte, Kristiane Hallermann, Alexandra Krause, Corinna Brichta, Natascha van der Werf-Grohmann, Andreas Krebs, Henner Hanssen, Peter Deibert, Karl Otfried Schwab
RFC3.2
Personalized and predictive medicine for pediatric diabetes through a genetic test using next generation sequencing
Valerie Schwitzgebel, Philippe Klee, Mirjam Dirlewanger, Jean-Louis Blouin
Personalized and predictive medicine for pediatric diabetes through a genetic test using next generation sequencing
Valerie Schwitzgebel, Philippe Klee, Mirjam Dirlewanger, Jean-Louis Blouin
RFC3.3
Significant prevalence of severe monogenic immune defects among children with Type 1 diabetes and low T1D-genetic risk score
Stepanka Pruhova, Veronika Strakova, Lenka Elblova, Matthew B. Johnson, Petra Dusatkova, Barbora Obermannova, Lenka Petruzelkova, Stanislava Kolouskova, Marta Snajderova, Eva Fronkova, Michael Svaton, Jan Lebl, Andrew T. Hattersley, Zdenek Sumnik
Significant prevalence of severe monogenic immune defects among children with Type 1 diabetes and low T1D-genetic risk score
Stepanka Pruhova, Veronika Strakova, Lenka Elblova, Matthew B. Johnson, Petra Dusatkova, Barbora Obermannova, Lenka Petruzelkova, Stanislava Kolouskova, Marta Snajderova, Eva Fronkova, Michael Svaton, Jan Lebl, Andrew T. Hattersley, Zdenek Sumnik
RFC3.4
Functional characterization of a novel KLF11 mutation identified in a family with autoantibody-negative Type 1 Diabetes
Kikumi Ushijima, Tomoyuki Kawamura, Tsutomu Ogata, Ichiro Yokota, Shigetaka Sugihara, Satoshi Narumi, Maki Fukami
Functional characterization of a novel KLF11 mutation identified in a family with autoantibody-negative Type 1 Diabetes
Kikumi Ushijima, Tomoyuki Kawamura, Tsutomu Ogata, Ichiro Yokota, Shigetaka Sugihara, Satoshi Narumi, Maki Fukami
RFC3.5
Recent secular change in pre- and postnatal growth and adiposity in infants of mothers with Gestational Diabetes
Laurentya Olga, Philippa Prentice, Ieuan Hughes, Carlo Acerini, Ken Ong, David Dunger
Recent secular change in pre- and postnatal growth and adiposity in infants of mothers with Gestational Diabetes
Laurentya Olga, Philippa Prentice, Ieuan Hughes, Carlo Acerini, Ken Ong, David Dunger
RFC3.6
Treatment adherence and weight loss are key predictors of HbA1c one year after diagnosis of childhood Type 2 Diabetes in UK
Toby Candler, Osama Mahmoud, Richard Lynn, Abdalmonem Majbar, Timothy Barrett, Julian PH Shield
Treatment adherence and weight loss are key predictors of HbA1c one year after diagnosis of childhood Type 2 Diabetes in UK
Toby Candler, Osama Mahmoud, Richard Lynn, Abdalmonem Majbar, Timothy Barrett, Julian PH Shield
FC13.6
Teamwork saves lives: how pediatric multidisciplinary care can prevent ‘unexplained deaths’ in adults with Prader-Willi syndrome
Kirsten Davidse, Karlijn Pellikaan, Anna Rosenberg, Janneke Baan, Laura de Graaff
Teamwork saves lives: how pediatric multidisciplinary care can prevent ‘unexplained deaths’ in adults with Prader-Willi syndrome
Kirsten Davidse, Karlijn Pellikaan, Anna Rosenberg, Janneke Baan, Laura de Graaff
FC15.1
The diagnostic yield of a targeted next generation sequencing panel in children with short stature of undefined aetiology
Reena Perchard, Philip G Murray, Georgina L Highton, Andrew J Whatmore, Peter E Clayton
The diagnostic yield of a targeted next generation sequencing panel in children with short stature of undefined aetiology
Reena Perchard, Philip G Murray, Georgina L Highton, Andrew J Whatmore, Peter E Clayton
FC15.2
Effects of caloric restriction during gestation on the methylome of offspring’s adipose tissue and reversibility of such effects by metformin in a swine model
Silvia Xargay-Torrent, Gemma Carreras-Badosa, Joan Tibau, Josep Reixach, Esther Lizarraga-Mollinedo, Berta Mas-Pares, Anna Prats-Puig, Francis de Zegher, Lourdes Ibañez, Abel Lopez-Bermejo
Effects of caloric restriction during gestation on the methylome of offspring’s adipose tissue and reversibility of such effects by metformin in a swine model
Silvia Xargay-Torrent, Gemma Carreras-Badosa, Joan Tibau, Josep Reixach, Esther Lizarraga-Mollinedo, Berta Mas-Pares, Anna Prats-Puig, Francis de Zegher, Lourdes Ibañez, Abel Lopez-Bermejo
FC15.3
Methylation of the C19MC microRNA locus in the placenta: a mechanism whereby maternal body size links to that of the child
Silvia Xargay-Torrent, Anna Prats-Puig, Berta Mas-Pares, Judit Bassols, Clive J Petry, Michael Girardot, Francis de Zegher, Lourdes Ibañez, David B Dunger, Robert Feil, Abel Lopez-Bermejo
Methylation of the C19MC microRNA locus in the placenta: a mechanism whereby maternal body size links to that of the child
Silvia Xargay-Torrent, Anna Prats-Puig, Berta Mas-Pares, Judit Bassols, Clive J Petry, Michael Girardot, Francis de Zegher, Lourdes Ibañez, David B Dunger, Robert Feil, Abel Lopez-Bermejo
FC15.4
The metabolic profile associated with RASopathies
Renata Noronha, Thais Homma, Michelle Moraes, Edoarda Albuquerque, Mariana Funari, Alexandre Pereira, Sandra Villares, Debora Bertola, Alexander Jorge, Alexsandra Malaquias
The metabolic profile associated with RASopathies
Renata Noronha, Thais Homma, Michelle Moraes, Edoarda Albuquerque, Mariana Funari, Alexandre Pereira, Sandra Villares, Debora Bertola, Alexander Jorge, Alexsandra Malaquias
FC15.5
Utility of BDNF and MMP-1 as markers of cardiometabolic risk in Turner Syndrome girls
Ewa Błaszczyk, Lorek Miłosz, Tomasz Francuz, Joanna Gieburowska, Aneta Gawlik
Utility of BDNF and MMP-1 as markers of cardiometabolic risk in Turner Syndrome girls
Ewa Błaszczyk, Lorek Miłosz, Tomasz Francuz, Joanna Gieburowska, Aneta Gawlik
FC15.6
Vosoritide for children with Achondroplasia:a 30 month update from an ongoing Phase 2 Clinical Trial
Melita Irving, Julie Hoover-Fong, Carlos Bacino, Joel Charrow, Valerie Cormier-Daire, Patti Dickson, Paul Harmatz, Alice Huntsman Labed, Kala Jayaram, George Jeha, Jonathan Day, Kevin Larimore, John Phillips, Ravi Savarirayan
Vosoritide for children with Achondroplasia:a 30 month update from an ongoing Phase 2 Clinical Trial
Melita Irving, Julie Hoover-Fong, Carlos Bacino, Joel Charrow, Valerie Cormier-Daire, Patti Dickson, Paul Harmatz, Alice Huntsman Labed, Kala Jayaram, George Jeha, Jonathan Day, Kevin Larimore, John Phillips, Ravi Savarirayan
FC4.5
Prediction of adult height by artificial intelligence (AI) through machine learning (ML) from early height data
Michael Shmoish, Alina German, Nurit Devir, Anna Hecht, Gary Butler, Aimon Niklasson, Kerstin Albertsson-Wikland, Ze'ev Hochberg
Prediction of adult height by artificial intelligence (AI) through machine learning (ML) from early height data
Michael Shmoish, Alina German, Nurit Devir, Anna Hecht, Gary Butler, Aimon Niklasson, Kerstin Albertsson-Wikland, Ze'ev Hochberg
FC4.6
Absorption and excretion of Somapacitan, a long-acting Growth Hormone (GH) derivative
Michael Højby Rasmussen, Birgitte Bentz Damholt, Hans Helleberg, Mads Bjelke, Swapna Suresh, Rasmus Vestergaard Juul, Christian Hollensen
Absorption and excretion of Somapacitan, a long-acting Growth Hormone (GH) derivative
Michael Højby Rasmussen, Birgitte Bentz Damholt, Hans Helleberg, Mads Bjelke, Swapna Suresh, Rasmus Vestergaard Juul, Christian Hollensen
LB-P2
Effects on growth, body composition and gross motor and cognitive development and safety of recombinant human growth hormone in infants or toddlers with Prader-Willi syndrome: A randomized, active-comparator controlled Trial
Ji-Eun Lee, Aram Yang, Jin-Ho Choi, Young Bae Sohn, Han-Wook Yoo, Dong-Kyu Jin
Effects on growth, body composition and gross motor and cognitive development and safety of recombinant human growth hormone in infants or toddlers with Prader-Willi syndrome: A randomized, active-comparator controlled Trial
Ji-Eun Lee, Aram Yang, Jin-Ho Choi, Young Bae Sohn, Han-Wook Yoo, Dong-Kyu Jin
LB-P3
Glycemic Impact of Long Term Use of Diazoxide Choline Controlled-Release Tablets in Patients with Prader-Willi Syndrome or with Very High Triglycerides
Virginia Kimonis, JA Gold, RW Charlton, Neil Cowen, JL Miller
Glycemic Impact of Long Term Use of Diazoxide Choline Controlled-Release Tablets in Patients with Prader-Willi Syndrome or with Very High Triglycerides
Virginia Kimonis, JA Gold, RW Charlton, Neil Cowen, JL Miller
LB-P8
Pharmacokinetics of Diazoxide Choline Controlled-Release Tablets, a Once Daily Treatment Being Evaluation in Patients with Prader Willi Syndrome
Parisa Salehi, RW Charlton, Neil Cowen
Pharmacokinetics of Diazoxide Choline Controlled-Release Tablets, a Once Daily Treatment Being Evaluation in Patients with Prader Willi Syndrome
Parisa Salehi, RW Charlton, Neil Cowen
P1-P159
Does X-chromosome gene dosage determine growth and phenotypic features in Turner syndrome with 45,X/46,XX mosaicism on standard karyotyping? A cross-sectional analysis of the French national rare disease network database
Elodie Fiot, Delphine Zénaty, Paul Pick, Patricia Boizeau, Jeremy Haignere, Sophie Dos Santos, Sophie Christin-Maitre, Jean-Claude Carel, Juliane Léger, French Turner Syndrome Study Group
Does X-chromosome gene dosage determine growth and phenotypic features in Turner syndrome with 45,X/46,XX mosaicism on standard karyotyping? A cross-sectional analysis of the French national rare disease network database
Elodie Fiot, Delphine Zénaty, Paul Pick, Patricia Boizeau, Jeremy Haignere, Sophie Dos Santos, Sophie Christin-Maitre, Jean-Claude Carel, Juliane Léger, French Turner Syndrome Study Group
P1-P160
To freeze or not to freeze? First clinical experiences on fertility preservation in girls with Turner syndrome
Myra Schleedoorn, Kathrin Fleischer, Didi Braat, Catharina Beerendonk, Ron van Golde, Ron Peek, Janielle van Alfen - van der Velden
To freeze or not to freeze? First clinical experiences on fertility preservation in girls with Turner syndrome
Myra Schleedoorn, Kathrin Fleischer, Didi Braat, Catharina Beerendonk, Ron van Golde, Ron Peek, Janielle van Alfen - van der Velden
P1-P161
Analysis of osteoblats precursors in girls with Turner Syndrome
Giacomina Brunetti, Mariangela Chiarito, Laura Piacente, Gabriella Aceto, Silvia Colucci, Graziana Colaianni, Maria Grano, Gabriele D'Amato, Maria Felicia Faienza
Analysis of osteoblats precursors in girls with Turner Syndrome
Giacomina Brunetti, Mariangela Chiarito, Laura Piacente, Gabriella Aceto, Silvia Colucci, Graziana Colaianni, Maria Grano, Gabriele D'Amato, Maria Felicia Faienza
P1-P162
Comparing the cumulative dose of growth hormone therapy using body weight-based dosing versus body surface area-based dosing in children with Turner syndrome—data from the ANSWER study
Philippe Backeljauw, Mitchell Geffner, Judith Ross, Natalia Holot, Vlady Ostrow
Comparing the cumulative dose of growth hormone therapy using body weight-based dosing versus body surface area-based dosing in children with Turner syndrome—data from the ANSWER study
Philippe Backeljauw, Mitchell Geffner, Judith Ross, Natalia Holot, Vlady Ostrow
P1-P163
The Association between Growth Hormone dose and short-term height outcomes in a large cohort of paediatric patients with Turner syndrome: real-world data from the NordiNet® International Outcome Study (IOS) and ANSWER Program
Jo Blair, Tilman R. Rohrer, Birgitte Tønnes Pedersen, Sebastian Roehrich, Philippe Backeljauw
The Association between Growth Hormone dose and short-term height outcomes in a large cohort of paediatric patients with Turner syndrome: real-world data from the NordiNet® International Outcome Study (IOS) and ANSWER Program
Jo Blair, Tilman R. Rohrer, Birgitte Tønnes Pedersen, Sebastian Roehrich, Philippe Backeljauw
P1-P164
Changing patterns of growth in Prader-Willi syndrome
Georgia Irene Neophytou, Mikaela Frixou, M Guftar Shaikh, Andreas Kyriakou
Changing patterns of growth in Prader-Willi syndrome
Georgia Irene Neophytou, Mikaela Frixou, M Guftar Shaikh, Andreas Kyriakou
P1-P165
Sleep-disordered breathing in children with Prader-Willi syndrome in relation to Growth Hormone Therapy onset
Maja Zimmermann, Constance Laemmer, Joachim Woelfle, Bettina Goihlke
Sleep-disordered breathing in children with Prader-Willi syndrome in relation to Growth Hormone Therapy onset
Maja Zimmermann, Constance Laemmer, Joachim Woelfle, Bettina Goihlke
P1-P166
Safety and effectiveness of growth hormone treatment in patients with Prader-Willi Syndrome under 2 years of age in a reference hospital
Raquel Corripio, Carla Tubau, Nuria Cahis, Jacobo Pérez, Josefa Rivera, Elisabeth Gabau
Safety and effectiveness of growth hormone treatment in patients with Prader-Willi Syndrome under 2 years of age in a reference hospital
Raquel Corripio, Carla Tubau, Nuria Cahis, Jacobo Pérez, Josefa Rivera, Elisabeth Gabau
P1-P167
Improved mental and motor development during 3 years of GH treatment in very young children with Prader-Willi syndrome
Stephany Donze, Layla Damen, Eva Mahabier, Anita Hokken-Koelega
Improved mental and motor development during 3 years of GH treatment in very young children with Prader-Willi syndrome
Stephany Donze, Layla Damen, Eva Mahabier, Anita Hokken-Koelega
P1-P168
GH response to GHRH and Arginine in previously GH-treated young adults with Prader-Willi syndrome
Stephany Donze, Layla Damen, Anita Hokken-Koelega
GH response to GHRH and Arginine in previously GH-treated young adults with Prader-Willi syndrome
Stephany Donze, Layla Damen, Anita Hokken-Koelega
P1-P169
A novel type of pubertal height, weight, and BMI reference, aligned for onset of puberty
Kerstin Albertsson-Wikland, Aimon Niklasson, Lars Gelander, Anton Holmgren, Stefan Aronson, Agneta Sjöberg, Lauren Lissner
A novel type of pubertal height, weight, and BMI reference, aligned for onset of puberty
Kerstin Albertsson-Wikland, Aimon Niklasson, Lars Gelander, Anton Holmgren, Stefan Aronson, Agneta Sjöberg, Lauren Lissner
P1-P170
Evaluating cut-offs for automatic growth screening in Swedish children – using the Finnish growth monitoring algorithm
Lars Gelander, Aimon Niklasson, Anton Holmgren, Antti Saari, Leo Dunkel, Kerstin Albertsson-Wikland
Evaluating cut-offs for automatic growth screening in Swedish children – using the Finnish growth monitoring algorithm
Lars Gelander, Aimon Niklasson, Anton Holmgren, Antti Saari, Leo Dunkel, Kerstin Albertsson-Wikland
P1-P171
Prospective study of growth in Swedish children treated with modified ketogenic diet
Anna Svedlund, Tove Hallböök, Per Magnusson, Jovanna Dahlgren, Diana Swolin-Eide
Prospective study of growth in Swedish children treated with modified ketogenic diet
Anna Svedlund, Tove Hallböök, Per Magnusson, Jovanna Dahlgren, Diana Swolin-Eide
P1-P172
Early gut microbiota and childhood growth
Kasper Schei, Saideh Salamati, Petur Benedikt Juliusson, Torbjørn Øien, Knut Rudi, Rønnaug Astri Ødegård
Early gut microbiota and childhood growth
Kasper Schei, Saideh Salamati, Petur Benedikt Juliusson, Torbjørn Øien, Knut Rudi, Rønnaug Astri Ødegård
P1-P173
Clinical and radiological manifestations in a large Swedish family with a pathogenic heterozygous ACAN variant
Alexandra Gkourogianni, Emma Segerlund, Sigrun Hallgrimsdottir, Ola Nilsson, Eva-Lena Stattin
Clinical and radiological manifestations in a large Swedish family with a pathogenic heterozygous ACAN variant
Alexandra Gkourogianni, Emma Segerlund, Sigrun Hallgrimsdottir, Ola Nilsson, Eva-Lena Stattin
P1-P174
Identification of ADAMTS6 as a novel candidate gene for Idiopathic Short Stature with advanced bone maturation
Diana M Warman, Pablo Ramirez, Roxana Marino, Natalia Perez Garrido, Maria Sol Touzon, Matias Pujana Pentreath, Maria Celeste Mattone, Marco Rivarola, Alicia Belgorosky
Identification of ADAMTS6 as a novel candidate gene for Idiopathic Short Stature with advanced bone maturation
Diana M Warman, Pablo Ramirez, Roxana Marino, Natalia Perez Garrido, Maria Sol Touzon, Matias Pujana Pentreath, Maria Celeste Mattone, Marco Rivarola, Alicia Belgorosky
P1-P175
Dual function of the retinoic acid catabolizing enzyme CYP26C1 – underlying idiopathic short stature and modifying disease severity in SHOX deficiency
Antonino Montalbano, Lonny Juergensen, Maki Fukami, Christian T Thiel, Nadine H Hauer, Susanne Fricke-Otto, Gerhard Binder, Y Naiki, Tsutomu Ogata, David Hassel, Gudrun A Rappold
Dual function of the retinoic acid catabolizing enzyme CYP26C1 – underlying idiopathic short stature and modifying disease severity in SHOX deficiency
Antonino Montalbano, Lonny Juergensen, Maki Fukami, Christian T Thiel, Nadine H Hauer, Susanne Fricke-Otto, Gerhard Binder, Y Naiki, Tsutomu Ogata, David Hassel, Gudrun A Rappold
P1-P176
Growth plate disorders are the main cause of severe familiar short stature in children classified and treated with growth hormone as SGA or GHD
Lukáš Plachý, Veronika Straková, Lenka Elblová, Petra Dušátková, Barbora Obermannová, Marta Šnajderová, Stanislava Koloušková, Dana Zemková, Zdeněk Šumník, Jan Lebl, Štěpánka Průhová
Growth plate disorders are the main cause of severe familiar short stature in children classified and treated with growth hormone as SGA or GHD
Lukáš Plachý, Veronika Straková, Lenka Elblová, Petra Dušátková, Barbora Obermannová, Marta Šnajderová, Stanislava Koloušková, Dana Zemková, Zdeněk Šumník, Jan Lebl, Štěpánka Průhová
P1-P177
Genetic investigation of children with syndromic prenatal onset short stature
Thais Homma, Bruna Freire, Rachel Ronjo, Andrew Dauber, Mariana Funari, Antônio Lerario, Ivo Arnhold, Ana Canton, Sofia Sugayama, Debora Bertola, Chong Kim, Alexsandra Malaquias, Alexander Jorge
Genetic investigation of children with syndromic prenatal onset short stature
Thais Homma, Bruna Freire, Rachel Ronjo, Andrew Dauber, Mariana Funari, Antônio Lerario, Ivo Arnhold, Ana Canton, Sofia Sugayama, Debora Bertola, Chong Kim, Alexsandra Malaquias, Alexander Jorge
P1-P178
Identification of three novel mutations in 10 pediatric patients with unexplained syndromic short stature identified by targeted exome sequencing in Korea
CHONG KUN CHEON, Yoo-Mi Kim
Identification of three novel mutations in 10 pediatric patients with unexplained syndromic short stature identified by targeted exome sequencing in Korea
CHONG KUN CHEON, Yoo-Mi Kim
P1-P179
Beckwith Wiedemann syndrome: first international consensus regarding diagnosis and clinical management
Frederic Brioude, Jennifer M. Kalish, Alessandro Mussa, Alison C. Foster, Jet Bliek, Giovanni B. Ferrero, Susanne E. Boonen, Robert Baker, Monica Bertoletti, Guido Cocchi, Carole Coze, Maurizio De Pellegrin, Khalid Hussain, Malgorzata Krajewska-Walasek, Christian P. Kratz, Yves Le Bouc, Saskia M. Maas, Katrin Ounap, Licia Peruzzi, Sylvie Rossignol, Silvia Russo, Caroleen Shipster, Agata Skorka, Katrina Tatton-Brown, Jair Tenorio, Chiara Tortora, Karen Gronskov, Irene Netchine, Raoul C. Hennekam, Dirk Prawitt, Zeynep Tümer, Thomas Eggermann, Deborah J. G. Mackay, Andrea Riccio, Eamonn R. Maher
Beckwith Wiedemann syndrome: first international consensus regarding diagnosis and clinical management
Frederic Brioude, Jennifer M. Kalish, Alessandro Mussa, Alison C. Foster, Jet Bliek, Giovanni B. Ferrero, Susanne E. Boonen, Robert Baker, Monica Bertoletti, Guido Cocchi, Carole Coze, Maurizio De Pellegrin, Khalid Hussain, Malgorzata Krajewska-Walasek, Christian P. Kratz, Yves Le Bouc, Saskia M. Maas, Katrin Ounap, Licia Peruzzi, Sylvie Rossignol, Silvia Russo, Caroleen Shipster, Agata Skorka, Katrina Tatton-Brown, Jair Tenorio, Chiara Tortora, Karen Gronskov, Irene Netchine, Raoul C. Hennekam, Dirk Prawitt, Zeynep Tümer, Thomas Eggermann, Deborah J. G. Mackay, Andrea Riccio, Eamonn R. Maher
P1-P180
Silver Russell and Beckwith-Wiedemann syndromes: Mosaic distribution of epigenetic anomalies
Aurelie PHAM, Eloise Giabicani, Virginie Steunou, Irène Netchine, Frederic Brioude
Silver Russell and Beckwith-Wiedemann syndromes: Mosaic distribution of epigenetic anomalies
Aurelie PHAM, Eloise Giabicani, Virginie Steunou, Irène Netchine, Frederic Brioude
P1-P181
Long term effects of childhood growth hormone treatment on height and body mass index in adolescents and adults with Silver-Russell syndrome
Oluwakemi Lokulo-Sodipe, Ana P. M. Canton, Eloise Giabicani, Nawfel Ferrand, Jenny Child, Emma L. Wakeling, Gerhard Binder, Irène Netchine, Deborah J.G. Mackay, Hazel M. Inskip, Christopher D. Byrne, Justin H. Davies, I. Karen Temple
Long term effects of childhood growth hormone treatment on height and body mass index in adolescents and adults with Silver-Russell syndrome
Oluwakemi Lokulo-Sodipe, Ana P. M. Canton, Eloise Giabicani, Nawfel Ferrand, Jenny Child, Emma L. Wakeling, Gerhard Binder, Irène Netchine, Deborah J.G. Mackay, Hazel M. Inskip, Christopher D. Byrne, Justin H. Davies, I. Karen Temple
P1-P182
Year-one Effectiveness and Overall Safety of NutropinAq® for Growth Hormone Deficiency (GHD) and Other Paediatric Growth Disorders: Completion of the International Cooperative Growth Study (iNCGS) European Registry
Regis Coutant, Jordi Bosch Muñoz, Cristina Dumitrescu, Dirk Schnabel, Caroline Sert, Valerie Perrot, Mehul Dattani
Year-one Effectiveness and Overall Safety of NutropinAq® for Growth Hormone Deficiency (GHD) and Other Paediatric Growth Disorders: Completion of the International Cooperative Growth Study (iNCGS) European Registry
Regis Coutant, Jordi Bosch Muñoz, Cristina Dumitrescu, Dirk Schnabel, Caroline Sert, Valerie Perrot, Mehul Dattani
P1-P183
Carriers of IGF1-receptor mutations as a subgroup of SGA patients: a comprehensive retrospective comparison of response to rhGH treatment and health profile
Eric Göpel, Jürgen Klammt, Denise Rockstroh, Heike Pfäffle, Marina Schlicke, Susanne Bechtold-Dalla Pozza, Marie-Hélène Gannagé-Yared, Zoran Gucev, Angelika Mohn, Eva-Maria Harmel, Julia Volkmann, Holger Bogatsch, Christoph Beger, Ruth Gausche, Susann Weihrauch-Blüher, Roland Pfäffle
Carriers of IGF1-receptor mutations as a subgroup of SGA patients: a comprehensive retrospective comparison of response to rhGH treatment and health profile
Eric Göpel, Jürgen Klammt, Denise Rockstroh, Heike Pfäffle, Marina Schlicke, Susanne Bechtold-Dalla Pozza, Marie-Hélène Gannagé-Yared, Zoran Gucev, Angelika Mohn, Eva-Maria Harmel, Julia Volkmann, Holger Bogatsch, Christoph Beger, Ruth Gausche, Susann Weihrauch-Blüher, Roland Pfäffle
P1-P184
Characteristics, effectiveness and safety data for patients with growth failure treated with recombinant IGF-I (rhIGF-I) and achieving adult or near-adult height (AH): results from the European Increlex® Growth Forum Database (EU-IGFD) registry
Michel Polak, Joachim Woelfle, Valerie Perrot, Caroline Sert, Peter Bang
Characteristics, effectiveness and safety data for patients with growth failure treated with recombinant IGF-I (rhIGF-I) and achieving adult or near-adult height (AH): results from the European Increlex® Growth Forum Database (EU-IGFD) registry
Michel Polak, Joachim Woelfle, Valerie Perrot, Caroline Sert, Peter Bang
P1-P185
Growth outcome in girls with idiopathic central precocious puberty treated with gonadotropin-releasing hormone agonist
Hae Sang Lee, Jin Soon Hwang
Growth outcome in girls with idiopathic central precocious puberty treated with gonadotropin-releasing hormone agonist
Hae Sang Lee, Jin Soon Hwang
P1-P186
Maternal uniparental disomy for chromosome 20: physical and endocrinological characteristics of six patients
Sayaka Kawashima, Akie Nakamura, Takanobu Inoue, Keiko Matsubara, Reiko Horikawa, Keiko Wakui, Kyoko Takano, Yoshimitsu Fukushima, Toshi Tatematsu, Seiji Mizuno, Junko Tsubaki, Shigeo Kure, Yoichi Matsubara, Tsutomu Ogata, Keisuke Nagasaki, Maki Fukami, Masayo Kagami
Maternal uniparental disomy for chromosome 20: physical and endocrinological characteristics of six patients
Sayaka Kawashima, Akie Nakamura, Takanobu Inoue, Keiko Matsubara, Reiko Horikawa, Keiko Wakui, Kyoko Takano, Yoshimitsu Fukushima, Toshi Tatematsu, Seiji Mizuno, Junko Tsubaki, Shigeo Kure, Yoichi Matsubara, Tsutomu Ogata, Keisuke Nagasaki, Maki Fukami, Masayo Kagami
P1-P187
A novel deadly variant in the TP53 gene causing Li-Fraumeni Syndrome. The importance of clinical awareness and the contribution of molecular diagnosis in active prevention within families with multiple tumor incidents at a young age.
Christina Bothou, Georgios P. Spyridis, Dionysios A. Papantonatos, Constantine A. Stratakis, Dimitrios T. Papadimitriou
A novel deadly variant in the TP53 gene causing Li-Fraumeni Syndrome. The importance of clinical awareness and the contribution of molecular diagnosis in active prevention within families with multiple tumor incidents at a young age.
Christina Bothou, Georgios P. Spyridis, Dionysios A. Papantonatos, Constantine A. Stratakis, Dimitrios T. Papadimitriou
P1-P188
Mutations in SHOX, GHR and IGFALS genes among Indian children with 'idiopathic short stature'
Anil Kumar, Vandana Jain
Mutations in SHOX, GHR and IGFALS genes among Indian children with 'idiopathic short stature'
Anil Kumar, Vandana Jain
P2-P239
Heart and aorta anomalies in Turner Syndrome and relation with karyotype
Aslı Derya Kardelen, Feyza Darendeliler, Genco Gençay, Zuhal İnce, Behruz Aliyev, Esin Karakılıç Özturan, Zehra Yavaş Abalı, Şükran Poyrazoğlu, Kemal Nişli, Firdevs Baş
Heart and aorta anomalies in Turner Syndrome and relation with karyotype
Aslı Derya Kardelen, Feyza Darendeliler, Genco Gençay, Zuhal İnce, Behruz Aliyev, Esin Karakılıç Özturan, Zehra Yavaş Abalı, Şükran Poyrazoğlu, Kemal Nişli, Firdevs Baş
P2-P240
The validation of an automated bone age assessment in girls with Turner syndrome – a pilot study
Ondrej Soucek, Jan Lebl, Klara Maratova, Dana Zemkova, Zdenek Sumnik
The validation of an automated bone age assessment in girls with Turner syndrome – a pilot study
Ondrej Soucek, Jan Lebl, Klara Maratova, Dana Zemkova, Zdenek Sumnik
P2-P241
Turner Syndrome and Autoimmune Thyroid Disease: pecularities of evolution in 93 Turner Syndrome patients
CRISTINA DUMITRESCU, IULIANA GHERLAN, LIDIA RADOMIR, MADALINA VINTILA, ANDREEA BREHAR, ANDRA CARAGHEORGHEOPOL, MARIANA PURICE, CAMELIA PROCOPIUC
Turner Syndrome and Autoimmune Thyroid Disease: pecularities of evolution in 93 Turner Syndrome patients
CRISTINA DUMITRESCU, IULIANA GHERLAN, LIDIA RADOMIR, MADALINA VINTILA, ANDREEA BREHAR, ANDRA CARAGHEORGHEOPOL, MARIANA PURICE, CAMELIA PROCOPIUC
P2-P242
Unusual clinical manifestations in Turner syndrome
Natallia Akulevich, Yulia Makarava, Larissa Ershova, Irina Kunavitch
Unusual clinical manifestations in Turner syndrome
Natallia Akulevich, Yulia Makarava, Larissa Ershova, Irina Kunavitch
P2-P243
Effect of combined growth hormone and estrogen treatment on the lipid profile and systolic function of the left ventricle in girls with Turner syndrome (TS)
Tatiana Shiryaeva, Elena Nagaeva, Maria Pankratova, Olga Chikulaeva, Natalia Volevodz, Valentina Peterkova
Effect of combined growth hormone and estrogen treatment on the lipid profile and systolic function of the left ventricle in girls with Turner syndrome (TS)
Tatiana Shiryaeva, Elena Nagaeva, Maria Pankratova, Olga Chikulaeva, Natalia Volevodz, Valentina Peterkova
P2-P244
Familial Turner Syndrome: Case Report
Jimena Lopez Dacal, Mercedes Villanueva, Rosa Enacán, Oscar Brunetto, Veronica Figueroa
Familial Turner Syndrome: Case Report
Jimena Lopez Dacal, Mercedes Villanueva, Rosa Enacán, Oscar Brunetto, Veronica Figueroa
P2-P245
Clinical review of 7 patients affected with 49,XXXXY syndrome
Jacobo Perez Sanchez, Raquel Corripio Collado, Concepcion Escofet, Carme Brun, Elisabeth Gabau
Clinical review of 7 patients affected with 49,XXXXY syndrome
Jacobo Perez Sanchez, Raquel Corripio Collado, Concepcion Escofet, Carme Brun, Elisabeth Gabau
P2-P246
Poor weight gain in Prader-Willi Syndrome – not always over-restriction consider Coeliac Disease
M Lateva, A Kassim, C Meade, R Maher, A McCrann, E Roche
Poor weight gain in Prader-Willi Syndrome – not always over-restriction consider Coeliac Disease
M Lateva, A Kassim, C Meade, R Maher, A McCrann, E Roche
P2-P247
Growth Hormone Unmasked Laryngomalacia and worsened Obstructive Sleep Apnea in infants with Prader-Willi Syndrome
Parisa Salehi, Joanna E. Wrede, Kaalan E. Johnson, Maida L. Chen
Growth Hormone Unmasked Laryngomalacia and worsened Obstructive Sleep Apnea in infants with Prader-Willi Syndrome
Parisa Salehi, Joanna E. Wrede, Kaalan E. Johnson, Maida L. Chen
P2-P248
How frequent are growth charts used in paediatric clinics? An audit of growth chart use in a district general hospital in Scotland
Andrew Punton, Nicola Britton, Jiohn Schulga
How frequent are growth charts used in paediatric clinics? An audit of growth chart use in a district general hospital in Scotland
Andrew Punton, Nicola Britton, Jiohn Schulga
P2-P249
GrowInform – a campaign for early diagnosis and treatment of growth disorders
Rosica Stoycheva, Violeta Iotova, Sonya Galcheva, Galina Yordanova, Kaloyan Tsochev, Antoaneta Ivanova, Teodora Karamfilova
GrowInform – a campaign for early diagnosis and treatment of growth disorders
Rosica Stoycheva, Violeta Iotova, Sonya Galcheva, Galina Yordanova, Kaloyan Tsochev, Antoaneta Ivanova, Teodora Karamfilova
P2-P250
Growth and body composition of term healthy Indian infants from birth to 2 years of age
Vandana Jain, Brijesh Kumar, Anura Kurpad
Growth and body composition of term healthy Indian infants from birth to 2 years of age
Vandana Jain, Brijesh Kumar, Anura Kurpad
P2-P251
Growth, body composition and metabolic parameters during childhood in a cohort of children born with a small for gestational age
M. Loredana Marcovecchio, Samantha Gorman, Peter Murgatroyd, Ken Ong, David Dunger, Kathryn Beardsall
Growth, body composition and metabolic parameters during childhood in a cohort of children born with a small for gestational age
M. Loredana Marcovecchio, Samantha Gorman, Peter Murgatroyd, Ken Ong, David Dunger, Kathryn Beardsall
P2-P252
Final results of NordiNet® International Outcome Study: key outcomes in paediatric patients
Michel Polak, Jo Blair, Tilman R. Rohrer, Alberto Pietropoli, Birgitte Tønnes Pedersen, Lars Savendahl
Final results of NordiNet® International Outcome Study: key outcomes in paediatric patients
Michel Polak, Jo Blair, Tilman R. Rohrer, Alberto Pietropoli, Birgitte Tønnes Pedersen, Lars Savendahl
P2-P253
INFLUENCE OF PUBERTY ON ADULT HEIGHT OF SGA CHILDREN TREATED WITH GH
Juan P. López-Siguero, Pablo Muñoz-Martinez, Mª Victoria Borrás-Pérez, Maria Alvarez-Casano, Sonia Sánchez-Moreno, Mª Jose Martinez-Aedo
INFLUENCE OF PUBERTY ON ADULT HEIGHT OF SGA CHILDREN TREATED WITH GH
Juan P. López-Siguero, Pablo Muñoz-Martinez, Mª Victoria Borrás-Pérez, Maria Alvarez-Casano, Sonia Sánchez-Moreno, Mª Jose Martinez-Aedo
P2-P254
Burden and impacts of daily recombinant Human Growth Hormone (r-hGH) injections in Growth Hormone Deficient (GHD) paediatric patients
Jane Loftus, Andreas Pleil, Roger Lamoureux, Diane Turner-Bowker, Andrew Yaworsky, Masami Kelly, Emily Love, Michelle McNamara, Andrew Palladino
Burden and impacts of daily recombinant Human Growth Hormone (r-hGH) injections in Growth Hormone Deficient (GHD) paediatric patients
Jane Loftus, Andreas Pleil, Roger Lamoureux, Diane Turner-Bowker, Andrew Yaworsky, Masami Kelly, Emily Love, Michelle McNamara, Andrew Palladino
P2-P255
Clinical and cost-effectiveness of GH treatment for children in Wales
Raluca-Monica Pop, Justin T. Warner, John W. Gregory
Clinical and cost-effectiveness of GH treatment for children in Wales
Raluca-Monica Pop, Justin T. Warner, John W. Gregory
P2-P256
Bone mineral density and body composition of young adults who were born small for gestational age and treated with growth hormone, after treatment completion
ANGELA ASCASO MATAMALA, LAURA TRUJILLANO LIDÓN, ANGELICA CALERO POLANCO, ANGEL MATUTE-LLORENTE, GLORIA BUENO LOZANO
Bone mineral density and body composition of young adults who were born small for gestational age and treated with growth hormone, after treatment completion
ANGELA ASCASO MATAMALA, LAURA TRUJILLANO LIDÓN, ANGELICA CALERO POLANCO, ANGEL MATUTE-LLORENTE, GLORIA BUENO LOZANO
P2-P257
Clinical effectiveness and cost-effectiveness of Somatropin treatment for short children in Egypt: analysis of 1-year data
Amany Ibrahim, Abeer Atef, Nora Badawy, Eatemad Helmy
Clinical effectiveness and cost-effectiveness of Somatropin treatment for short children in Egypt: analysis of 1-year data
Amany Ibrahim, Abeer Atef, Nora Badawy, Eatemad Helmy
P2-P258
Clinical and molecular analyses of 24 patients with Beckwith-Wiedemann Syndrome
WEI LU, BINGBING WU, WENHAO ZHOU, ZHANGQIAN ZHENG, MIAOYING ZHANG, RUOQIAN CHENG, FEIHONG LUO
Clinical and molecular analyses of 24 patients with Beckwith-Wiedemann Syndrome
WEI LU, BINGBING WU, WENHAO ZHOU, ZHANGQIAN ZHENG, MIAOYING ZHANG, RUOQIAN CHENG, FEIHONG LUO
P2-P259
Unusual case of combination of Beckwith-Wiedemann Syndrome and SHOX gene deficiency
Gilda Cassano, Sara Osimani, Roberta Pajno, Marco Pitea, Cristina Partenope, Silvia Russo, Gabriella Pozzobon
Unusual case of combination of Beckwith-Wiedemann Syndrome and SHOX gene deficiency
Gilda Cassano, Sara Osimani, Roberta Pajno, Marco Pitea, Cristina Partenope, Silvia Russo, Gabriella Pozzobon
P2-P260
An Irish regional study of Paediatric Growth Hormone Deficiency (CO-GHD): Classification of causes and factors associated with persistent GHD at transition
Mariana Grace, Caroline Joyce, Rose Morissey, Michael Moore, Susan O'Connell
An Irish regional study of Paediatric Growth Hormone Deficiency (CO-GHD): Classification of causes and factors associated with persistent GHD at transition
Mariana Grace, Caroline Joyce, Rose Morissey, Michael Moore, Susan O'Connell
P2-P261
Two different variants of short stature homeobox-containing gene (SHOX) mutation in the same family
Stefanie Graf, Maristella Santi, Monique Losekoot, Christa E. Flück
Two different variants of short stature homeobox-containing gene (SHOX) mutation in the same family
Stefanie Graf, Maristella Santi, Monique Losekoot, Christa E. Flück
P2-P262
Identification of a novel heterozygous ACAN mutation in a patient with non-syndromic short stature
Cristina Partenope, Dario Gallo, Chiara Maria Damia, Marta Adavastro, Lorenzo Fioretti, Marco Pitea, Giovanna Weber, Gabriella Pozzobon
Identification of a novel heterozygous ACAN mutation in a patient with non-syndromic short stature
Cristina Partenope, Dario Gallo, Chiara Maria Damia, Marta Adavastro, Lorenzo Fioretti, Marco Pitea, Giovanna Weber, Gabriella Pozzobon
P2-P263
Genetic investigation of Short Stature: a case report of Complex Constitutive rearrangement involving chromosome 15
Renata Machado Pinto, Lysa Bernardes Minasi, Irene Plaza Pinto, Juliana Ferreira da Silva, Damiana Mirian da Cruz Cunha, Cristiano Luiz Ribeiro, Cláudio Carlos da Silva, Aparecido Divino da Cruz
Genetic investigation of Short Stature: a case report of Complex Constitutive rearrangement involving chromosome 15
Renata Machado Pinto, Lysa Bernardes Minasi, Irene Plaza Pinto, Juliana Ferreira da Silva, Damiana Mirian da Cruz Cunha, Cristiano Luiz Ribeiro, Cláudio Carlos da Silva, Aparecido Divino da Cruz
P2-P264
Targeted/exome sequencing identified mutations in 55 Chinese children diagnosed with Noonan syndrome and a autosomal recessive form associated with LZTR1 variants
Xin Li, Ruen Yao, Yao Chen, Guoying Chang, Yu Ding, Juan Li, Yiping Shen, Xiumin Wang, Jian Wang
Targeted/exome sequencing identified mutations in 55 Chinese children diagnosed with Noonan syndrome and a autosomal recessive form associated with LZTR1 variants
Xin Li, Ruen Yao, Yao Chen, Guoying Chang, Yu Ding, Juan Li, Yiping Shen, Xiumin Wang, Jian Wang
P2-P265
A Novel Heterozygous Missense Variant in the LZTR1 Gene as a cause of Noonan Syndrome
Sumito Dateki, Satoshi Watanabe, Koh-ichiro Yoshiura, Hiroyuki Moriuchi
A Novel Heterozygous Missense Variant in the LZTR1 Gene as a cause of Noonan Syndrome
Sumito Dateki, Satoshi Watanabe, Koh-ichiro Yoshiura, Hiroyuki Moriuchi
P2-P266
A novel FGFR1 mutation in Kallmann syndrome with growth hormone deficiency
Gianluca Tornese, Maria Chiara Pellegrin, Matteo Pavan, Elena Faleschini, Egidio Barbi
A novel FGFR1 mutation in Kallmann syndrome with growth hormone deficiency
Gianluca Tornese, Maria Chiara Pellegrin, Matteo Pavan, Elena Faleschini, Egidio Barbi
P2-P267
Clinical and molecular characterization of eight Chinese children with Cornelia de Lange syndrome using targeted next generation sequencing
Guoying Chang
Clinical and molecular characterization of eight Chinese children with Cornelia de Lange syndrome using targeted next generation sequencing
Guoying Chang
P2-P268
A new mutation in IHH gene causing severe short stature
Adalgisa Festa, CATERINA LUONGO, ANNA GRANDONE, GRAZIA CIRILLO, FEDERICA GRECO, ANNALAURA TORELLA, VINCENZO NIGRO, EMANUELE MIRAGLIA DEL GIUDICE
A new mutation in IHH gene causing severe short stature
Adalgisa Festa, CATERINA LUONGO, ANNA GRANDONE, GRAZIA CIRILLO, FEDERICA GRECO, ANNALAURA TORELLA, VINCENZO NIGRO, EMANUELE MIRAGLIA DEL GIUDICE
P2-P269
CASE REPORT: ELLIS VAN CREVELD SYNDROME WITH A NOVEL MUTATION
Elif Söbü, Yasemin Kendir Demirkol, Gülay Can Yılmaz, Gül Demet Özçora, Fatma Yenigürbüz
CASE REPORT: ELLIS VAN CREVELD SYNDROME WITH A NOVEL MUTATION
Elif Söbü, Yasemin Kendir Demirkol, Gülay Can Yılmaz, Gül Demet Özçora, Fatma Yenigürbüz
P2-P270
A homozygous pathogenic variant in the TRHR gene in a boy who presented with severe familial short stature and central hypothyroidism
Marta Šnajderová, Lukáš Plachý, Veronika Straková, Lenka Elblová, Petra Dušátková, Dana Zemková, Jan Lebl, Štěpánka Průhová
A homozygous pathogenic variant in the TRHR gene in a boy who presented with severe familial short stature and central hypothyroidism
Marta Šnajderová, Lukáš Plachý, Veronika Straková, Lenka Elblová, Petra Dušátková, Dana Zemková, Jan Lebl, Štěpánka Průhová
P2-P272
Mild autistic spectrum disorder in a 33 year-old male Japanese patient with Temple syndrome
Shuichi Yatsuga, Masayo Kagami, Keiko Matsubara, Takuro Kimura, Chiho Yatsuga, Rio Mukasa, Takako Matsumoto, Yasutoshi Koga
Mild autistic spectrum disorder in a 33 year-old male Japanese patient with Temple syndrome
Shuichi Yatsuga, Masayo Kagami, Keiko Matsubara, Takuro Kimura, Chiho Yatsuga, Rio Mukasa, Takako Matsumoto, Yasutoshi Koga
P2-P273
Seventeen-year observation in a Japanese female case of Tatton-Brown-Rahman syndrome: an overgrowth syndrome with intellectual disability
Yoko Miyoshi, Keiko Yamamoto, Yukako Nakano, Kenichi Yamamoto, Takuo Kubota, Keiichi Ozono
Seventeen-year observation in a Japanese female case of Tatton-Brown-Rahman syndrome: an overgrowth syndrome with intellectual disability
Yoko Miyoshi, Keiko Yamamoto, Yukako Nakano, Kenichi Yamamoto, Takuo Kubota, Keiichi Ozono
P2-P275
Growth of infants born by Intracytoplasmic Sperm Injection (ICSI) technique
Ahmed Farouk Eldakrouri, Hamdy Alsayed Ali, Hilal Alrifai, Ashraf Soliman
Growth of infants born by Intracytoplasmic Sperm Injection (ICSI) technique
Ahmed Farouk Eldakrouri, Hamdy Alsayed Ali, Hilal Alrifai, Ashraf Soliman
P2-P276
Earlier mother’s age at menarche is a risk factor of daughter’s early menarche and short stature in young Korean female: Epidemiologic study
JUNG SUB LIM, JIN SOON HWANG
Earlier mother’s age at menarche is a risk factor of daughter’s early menarche and short stature in young Korean female: Epidemiologic study
JUNG SUB LIM, JIN SOON HWANG
P2-P277
Pulling the brakes — ‘Catch down growth’: a phenomenon for achieving mid‑parental height centile after acquired, all-cause, brain injury
Fabian B T Kraus, Peter C Hindmarsh, Helen A Spoudeas
Pulling the brakes — ‘Catch down growth’: a phenomenon for achieving mid‑parental height centile after acquired, all-cause, brain injury
Fabian B T Kraus, Peter C Hindmarsh, Helen A Spoudeas
P2-P278
Effects of inhaled corticosteroids and montelukast on growth and body mass index in children with asthma
ONUR AKIN, SULEYMAN TOLGA YAVUZ
Effects of inhaled corticosteroids and montelukast on growth and body mass index in children with asthma
ONUR AKIN, SULEYMAN TOLGA YAVUZ
P2-P279
Steroid management during hospital admissions in Duchenne Muscular Dystrophy
Kung-Ting Kao, Jennifer Dunne, Sasha Moonsammy, Shuko Joseph, Marina DiMarco, Sze Choong Wong
Steroid management during hospital admissions in Duchenne Muscular Dystrophy
Kung-Ting Kao, Jennifer Dunne, Sasha Moonsammy, Shuko Joseph, Marina DiMarco, Sze Choong Wong
P2-P280
Skeletal disproportion and growth impairment in glucocorticoid treated boys with Duchenne Muscular Dystrophy
Kung-Ting Kao, Shuko Joseph, Sarah Brown, Nadia Capaldi, Jennifer Dunne, Iain Horrocks, Marina DiMarco, Martin McMillan, Sheila Shepherd, Syed Faisal Ahmed, Sze Choong Wong
Skeletal disproportion and growth impairment in glucocorticoid treated boys with Duchenne Muscular Dystrophy
Kung-Ting Kao, Shuko Joseph, Sarah Brown, Nadia Capaldi, Jennifer Dunne, Iain Horrocks, Marina DiMarco, Martin McMillan, Sheila Shepherd, Syed Faisal Ahmed, Sze Choong Wong
P2-P281
A novel mutation in the SLC2A2 gene in a 19-year-old female with Diabetes Mellitus and Renal Tubular Acidosis:a therapeutic conundrum
Sanaa Sharari, Sara Al-Khawaga, Reem Hasnah, Saras Saraswathi, Basma Haris, Amira Saeed, Idris Mohammed, Riyaz Malik, Khalid Hussain
A novel mutation in the SLC2A2 gene in a 19-year-old female with Diabetes Mellitus and Renal Tubular Acidosis:a therapeutic conundrum
Sanaa Sharari, Sara Al-Khawaga, Reem Hasnah, Saras Saraswathi, Basma Haris, Amira Saeed, Idris Mohammed, Riyaz Malik, Khalid Hussain
P2-P282
Vesico-ureteral reflux and effect on growth indices
Georges Nicolas, Roula Hneineh, Marie-Claude Faddous Kalifeh
Vesico-ureteral reflux and effect on growth indices
Georges Nicolas, Roula Hneineh, Marie-Claude Faddous Kalifeh
P2-P283
A novel in frame deletion mutation in exon11 in BTK gene to X- linked agammaglobulinemia: case report and function analysis
hu xiaomei, yuan ke
A novel in frame deletion mutation in exon11 in BTK gene to X- linked agammaglobulinemia: case report and function analysis
hu xiaomei, yuan ke
P3-P219
IS GROWTH HORMONE DEFICIENCY A CONTRIBUTOR TO SHORT STATURE IN CUTIS LAXA SYNDROME?
Alice Albu, Irina Delia Nicolaescu, Denisa Dinca
IS GROWTH HORMONE DEFICIENCY A CONTRIBUTOR TO SHORT STATURE IN CUTIS LAXA SYNDROME?
Alice Albu, Irina Delia Nicolaescu, Denisa Dinca
P3-P220
Effect of Sickle Cell disease on growth and puberty
Anjumanara Omar, Fatma Abdallah, Beatrice Mutai
Effect of Sickle Cell disease on growth and puberty
Anjumanara Omar, Fatma Abdallah, Beatrice Mutai
P3-P222
Development of an online learn-pro module to support health care professionals knowledge about growth and puberty
Barbara Wardhaugh, Mohamad Guftat Shaikh, John Schulga
Development of an online learn-pro module to support health care professionals knowledge about growth and puberty
Barbara Wardhaugh, Mohamad Guftat Shaikh, John Schulga
P3-P223
Coeliac disease in Turner syndrome more frequent than expected
BAZ OUIDAD, SEMROUNI Mourad, SAKHER SAMIA, MIMOUNI ZERGUINI SAFIA
Coeliac disease in Turner syndrome more frequent than expected
BAZ OUIDAD, SEMROUNI Mourad, SAKHER SAMIA, MIMOUNI ZERGUINI SAFIA
P3-P224
A 14-year-old boy with Simpson- Golabi- Behmel syndrome- case report
Beata Sawicka, Anna Jakubiuk- Tomaszuk, Hanna Borysewicz- Sańczyk, Justyna Michalak, Artur Bossowski
A 14-year-old boy with Simpson- Golabi- Behmel syndrome- case report
Beata Sawicka, Anna Jakubiuk- Tomaszuk, Hanna Borysewicz- Sańczyk, Justyna Michalak, Artur Bossowski
P3-P225
Central precocious puberty in a girl with Silver Russell syndrome
Beata Wikiera, Julita Nocon-Bohusz, Anna Noczynska
Central precocious puberty in a girl with Silver Russell syndrome
Beata Wikiera, Julita Nocon-Bohusz, Anna Noczynska
P3-P226
Etiologies of short stature in pedaitric endocrine clinic in Northwest region (Trakya) of Turkey
Beyhan Özkaya, Emine Dilek, Diğdem Bezen, Fatma Özgüç Çömlek, Filiz Tütüncüler
Etiologies of short stature in pedaitric endocrine clinic in Northwest region (Trakya) of Turkey
Beyhan Özkaya, Emine Dilek, Diğdem Bezen, Fatma Özgüç Çömlek, Filiz Tütüncüler
P3-P227
Auditing presentation, investigations and management of Turner's syndrome
Buddhi Gunasekara, Dilusha Premathilaka, Raihana Hasheem, Udeni Kollurage, Janani Suntharesan, Rasarathinum Jeyanthakumar, Puvana Armugam, Navoda Atapattu
Auditing presentation, investigations and management of Turner's syndrome
Buddhi Gunasekara, Dilusha Premathilaka, Raihana Hasheem, Udeni Kollurage, Janani Suntharesan, Rasarathinum Jeyanthakumar, Puvana Armugam, Navoda Atapattu
P3-P228
Children born small for gestational age: catch-up growth during the first four years of life
Concepcion Freijo Martin, Laura Bertholt Zuber, inmaculada Palenzuela Revuelta
Children born small for gestational age: catch-up growth during the first four years of life
Concepcion Freijo Martin, Laura Bertholt Zuber, inmaculada Palenzuela Revuelta
P3-P229
A novel heterozygous pathogenic variant in PORCN gene causing focal dermal hypoplasia with short stature: case report and literature review
DI WU, XUYUN HU, XIAOQIAO LI, LIYA WEI, CHANG SU, JIAJIA CHEN, MIAO QIN, CHUNXIU GONG, YIPING SHEN
A novel heterozygous pathogenic variant in PORCN gene causing focal dermal hypoplasia with short stature: case report and literature review
DI WU, XUYUN HU, XIAOQIAO LI, LIYA WEI, CHANG SU, JIAJIA CHEN, MIAO QIN, CHUNXIU GONG, YIPING SHEN
P3-P230
Endocrinological evaluation of girls with Turner syndrome attending Alexandria University Children's Hospital
Doaa Khater, Shadia Eldesoky
Endocrinological evaluation of girls with Turner syndrome attending Alexandria University Children's Hospital
Doaa Khater, Shadia Eldesoky
P3-P231
A long follow-up in a young patient with Atypical Progeroid Syndrome
emanuela scarano, federica tamburrino, giovanna lattanzi, annamaria perri, Maria Elena Presicce, laura mazzanti
A long follow-up in a young patient with Atypical Progeroid Syndrome
emanuela scarano, federica tamburrino, giovanna lattanzi, annamaria perri, Maria Elena Presicce, laura mazzanti
P3-P232
GH treatment in Kabuki syndrome: a case report
Elisa Guidoni, Federica Lotti, Ursula Geronzi, Laura Arianna Sorrentino, Salvatore Grosso, Giovanna Municchi
GH treatment in Kabuki syndrome: a case report
Elisa Guidoni, Federica Lotti, Ursula Geronzi, Laura Arianna Sorrentino, Salvatore Grosso, Giovanna Municchi
P3-P233
GH treatment in oto-spondylo-megaepiphyseal dysplasia: a case report
Elisa Guidoni, Ursula Geronzi, Federica Lotti, Laura Arianna Sorrentino, Salvatore Grosso, Giovanna Municchi
GH treatment in oto-spondylo-megaepiphyseal dysplasia: a case report
Elisa Guidoni, Ursula Geronzi, Federica Lotti, Laura Arianna Sorrentino, Salvatore Grosso, Giovanna Municchi
P3-P234
Hepatic glycogen synthasedeficiency associated with growth hormone deficiency: a case report
Hakan Doneray, Ayse Ozden, Ilker Tosun
Hepatic glycogen synthasedeficiency associated with growth hormone deficiency: a case report
Hakan Doneray, Ayse Ozden, Ilker Tosun
P3-P235
Analysis of genetic mutations in a Chinese patient affected with Noonan Syndrome
YU YANG, Hui Huang
Analysis of genetic mutations in a Chinese patient affected with Noonan Syndrome
YU YANG, Hui Huang
P3-P236
A novel homozygous mutation in ERCC8 cause Cockayne Syndrome a in a Chinese family
Yu Yang, Hui Huang, Bin Zhou
A novel homozygous mutation in ERCC8 cause Cockayne Syndrome a in a Chinese family
Yu Yang, Hui Huang, Bin Zhou
P3-P237
Growth Hormon deficiency in identical twins with Gitelman Syndrome due to compound heterozygous mutation (p.R80fs*35/p.K957X ) of the SLC12A3 gene and the evaluation of the response to growth hormone replacement therapy
Betul Yaman, Kubra Celegen, Emine Korkmaz, Naz Guleray Lafci, Zeynep Balik, Huseyin Demirbilek, Ali Duzova
Growth Hormon deficiency in identical twins with Gitelman Syndrome due to compound heterozygous mutation (p.R80fs*35/p.K957X ) of the SLC12A3 gene and the evaluation of the response to growth hormone replacement therapy
Betul Yaman, Kubra Celegen, Emine Korkmaz, Naz Guleray Lafci, Zeynep Balik, Huseyin Demirbilek, Ali Duzova
P3-P238
Hypothyroidism and Growth Hormone (GH) deficiency,a spotlight on De Novo chromosomal 20p11.2 deletion
Idris Mohammed, Sara Al-Khawaga, Reem Hannah, Saras Saraswathi, Basma Haris, Amira Saeed, Sanaa Shararri, Khalid Hussain*
Hypothyroidism and Growth Hormone (GH) deficiency,a spotlight on De Novo chromosomal 20p11.2 deletion
Idris Mohammed, Sara Al-Khawaga, Reem Hannah, Saras Saraswathi, Basma Haris, Amira Saeed, Sanaa Shararri, Khalid Hussain*
P3-P239
Pharmacoeconomic and adherence analysis in growth hormone according to galenic presentation: in vivo study vs in vitro
Ignacio Diez-Lopez, Ainhoa Sarasua, Isabel Lorente, Ana Cristinaa Minguez, Carlos Martinez
Pharmacoeconomic and adherence analysis in growth hormone according to galenic presentation: in vivo study vs in vitro
Ignacio Diez-Lopez, Ainhoa Sarasua, Isabel Lorente, Ana Cristinaa Minguez, Carlos Martinez
P3-P240
The expression of cytokines in SGA children throughout lactation allows to characterize early the type of cath-up
Ignacio Diez-Lopez, Ainhoa Sarasua, Marta delHoyo, Isabel Lorente, Raquel Gomez de Segura, Minerva Picon, Asier Leniz, Alfredo Fernandez, Maria Puy-Portillo
The expression of cytokines in SGA children throughout lactation allows to characterize early the type of cath-up
Ignacio Diez-Lopez, Ainhoa Sarasua, Marta delHoyo, Isabel Lorente, Raquel Gomez de Segura, Minerva Picon, Asier Leniz, Alfredo Fernandez, Maria Puy-Portillo
P3-P241
Small Stature: A singular difference for accessing to job
Ignacio Diez-Lopez, Ainhoa Sarasua, Isabel Lorente, Manuel Carranza
Small Stature: A singular difference for accessing to job
Ignacio Diez-Lopez, Ainhoa Sarasua, Isabel Lorente, Manuel Carranza
P3-P242
A case of Hutchinson-Gilford Progeria Syndrome (HGPS) due to a pathogenic LMNA variant c.433G>A (p.Glu145Lys): Growth hormone administration failed to improve growth and long-term outcome
Ledjona Toni, Petra Dušátkoá, Dana Novotná, Dana Zemková, Štěpánka Průhová, Jan Lebl
A case of Hutchinson-Gilford Progeria Syndrome (HGPS) due to a pathogenic LMNA variant c.433G>A (p.Glu145Lys): Growth hormone administration failed to improve growth and long-term outcome
Ledjona Toni, Petra Dušátkoá, Dana Novotná, Dana Zemková, Štěpánka Průhová, Jan Lebl
P3-P243
Increased serum activity of liver aminotransferases in young patients with Turner Syndrome
Malgorzata Wojcik, Anna Ruszala, Dominika Janus, Krystyna Sztefko, Jerzy B. Starzyk
Increased serum activity of liver aminotransferases in young patients with Turner Syndrome
Malgorzata Wojcik, Anna Ruszala, Dominika Janus, Krystyna Sztefko, Jerzy B. Starzyk
P3-P244
Terner syndrome: Epidemiological study in Uzbekistan
Malika Mirkhaydarova, Nilufar Ibragimova
Terner syndrome: Epidemiological study in Uzbekistan
Malika Mirkhaydarova, Nilufar Ibragimova
P3-P245
SHOX HAPLOINSUFFICIENCY IN SHORT AND NOT SHORT CHILDREN: A SIGLE ITALIAN CETRE DATA
Maria Cristina Maggio, Saveria Sabrina Ragusa, Roberto Miceli, Giovanni Corsello
SHOX HAPLOINSUFFICIENCY IN SHORT AND NOT SHORT CHILDREN: A SIGLE ITALIAN CETRE DATA
Maria Cristina Maggio, Saveria Sabrina Ragusa, Roberto Miceli, Giovanni Corsello
P3-P246
Microduplication of 3p25.3 and 4p23 regions in a patient with multiple congenital anomalies, congenital hypothyroidism and adrenogenital syndrome
Massimo Barreca, Maria Scavone, Laura Giancotti, Emma Colao, Roberto Miniero
Microduplication of 3p25.3 and 4p23 regions in a patient with multiple congenital anomalies, congenital hypothyroidism and adrenogenital syndrome
Massimo Barreca, Maria Scavone, Laura Giancotti, Emma Colao, Roberto Miniero
P3-P247
A Rare Chromosomal Disorder, Trisomy 4p
Merve Nur Hepokur, Zeynep Uzan Tatlı, Gül Direk, Leyla Akın, Nihal Hatipoğlu, Mustafa Kendirci, Selim Kurtoğlu
A Rare Chromosomal Disorder, Trisomy 4p
Merve Nur Hepokur, Zeynep Uzan Tatlı, Gül Direk, Leyla Akın, Nihal Hatipoğlu, Mustafa Kendirci, Selim Kurtoğlu
P3-P248
Prediction of response to growth hormone treatment in Korean girls with Turner syndrome
Mo Kyung Jung, Se Young Kim, Ji-Eun Lee, Hae Soon Kim, Jeesuk Yu, Eun-Gyong Yoo
Prediction of response to growth hormone treatment in Korean girls with Turner syndrome
Mo Kyung Jung, Se Young Kim, Ji-Eun Lee, Hae Soon Kim, Jeesuk Yu, Eun-Gyong Yoo
P3-P249
A rare case of Turner Syndrome with the presence of the Y chromosome genetic material
Nadzeya Peskavaya, Anzhalika Solntsava, Katsyaryna Shlimakova
A rare case of Turner Syndrome with the presence of the Y chromosome genetic material
Nadzeya Peskavaya, Anzhalika Solntsava, Katsyaryna Shlimakova
P3-P250
Prader-Willi patient with rectal bleeding – experience in Center for Rare Endocrine Disordesrs in Varna, Bulagria
Nikolinka Yordanova, Violeta Iotova, Sonya Galcheva, Yuliya Bazdarska, Vilhelm Mladenov, Veselin Boyadzhiev
Prader-Willi patient with rectal bleeding – experience in Center for Rare Endocrine Disordesrs in Varna, Bulagria
Nikolinka Yordanova, Violeta Iotova, Sonya Galcheva, Yuliya Bazdarska, Vilhelm Mladenov, Veselin Boyadzhiev
P3-P251
Mosaicism 47XXX/45X0,a case report
Renata Machado Pinto, Sabrina Sara Moreira Duarte, Damiana Miriam da Cruz e Cunha, Cristiano Luiz Ribeiro, Cláudio Carlos da Silva, Aparecido Divino da Cruz, Alex Silva da Cruz
Mosaicism 47XXX/45X0,a case report
Renata Machado Pinto, Sabrina Sara Moreira Duarte, Damiana Miriam da Cruz e Cunha, Cristiano Luiz Ribeiro, Cláudio Carlos da Silva, Aparecido Divino da Cruz, Alex Silva da Cruz
P3-P252
Factors influencing the selection of injection areas during self-therapy for Growth Hormone Therapy among patients 10-15 years old
rotem diamant
Factors influencing the selection of injection areas during self-therapy for Growth Hormone Therapy among patients 10-15 years old
rotem diamant
P3-P253
Tall stature:a diagnosis is somtimes difficult
SAKINA KHERRA, Hadjira BEKAKCHA, Mounia Boutaba, Fatiha Talbi, Yasmina Behidj, Zoulikha Zeroual
Tall stature:a diagnosis is somtimes difficult
SAKINA KHERRA, Hadjira BEKAKCHA, Mounia Boutaba, Fatiha Talbi, Yasmina Behidj, Zoulikha Zeroual
P3-P254
Woodhouse-Sakati Syndrome: clinical and molecular study on a Qatari family with C2orf37 gene mutation
Sara Al-Khawaga, Amal Khalifa, Khalid Hussain*
Woodhouse-Sakati Syndrome: clinical and molecular study on a Qatari family with C2orf37 gene mutation
Sara Al-Khawaga, Amal Khalifa, Khalid Hussain*
P3-P255
Factors affecting height velocity in normal prepubertal children
Seul Ki Kim, Yujung Choi, Seonhwa Lee, Jun Hui Lee, Moon Bae Ahn, Shin Hee Kim, Won Kyung Cho, Kyung Soon Cho, Min Ho Jung, Byung Kyu Suh
Factors affecting height velocity in normal prepubertal children
Seul Ki Kim, Yujung Choi, Seonhwa Lee, Jun Hui Lee, Moon Bae Ahn, Shin Hee Kim, Won Kyung Cho, Kyung Soon Cho, Min Ho Jung, Byung Kyu Suh
P3-P256
Low dose Growth Hormone using IGF1 dose titration is associated with sustained optimal growth in a child with both Turner and Down Syndrome
Sharon Lim
Low dose Growth Hormone using IGF1 dose titration is associated with sustained optimal growth in a child with both Turner and Down Syndrome
Sharon Lim
P3-P257
Growth response in Noonan syndrome in Indian children
Smita Ramachandran, Aashish Sethi, Inderpal Kochar
Growth response in Noonan syndrome in Indian children
Smita Ramachandran, Aashish Sethi, Inderpal Kochar
P3-P258
Late referral of siblings with combined pituitary hormone deficiency (PROP1)
Snijezana Hasanbegovic, Amila Kljucic
Late referral of siblings with combined pituitary hormone deficiency (PROP1)
Snijezana Hasanbegovic, Amila Kljucic
P3-P259
17p13.1 Microduplication Syndrome in a child with familial short stature and growth hormone deficiency:a short case report
SOFIA LEKA-EMIRI, VASSILIOS PETROU, EMMANOUIL MANOLAKOS, ASPASIA FOTINOU, LORETTA THOMAIDIS, ELPIS VLACHOPAPADOPOULOU, STEFANOS MICHALACOS
17p13.1 Microduplication Syndrome in a child with familial short stature and growth hormone deficiency:a short case report
SOFIA LEKA-EMIRI, VASSILIOS PETROU, EMMANOUIL MANOLAKOS, ASPASIA FOTINOU, LORETTA THOMAIDIS, ELPIS VLACHOPAPADOPOULOU, STEFANOS MICHALACOS
P3-P261
Leri-Weill Syndrome phenotype with atypical cytogenetic finding
Vilhelm Mladenov, Violeta Iotova, Lydmila Angelova, Milena Stoyanova, Viktoria Bogdanova
Leri-Weill Syndrome phenotype with atypical cytogenetic finding
Vilhelm Mladenov, Violeta Iotova, Lydmila Angelova, Milena Stoyanova, Viktoria Bogdanova
P3-P262
Deletion of 12q12 increases the risk of growth retardation and intellectual disability
Ying Weng, Xiaoping Luo, Ling Hou
Deletion of 12q12 increases the risk of growth retardation and intellectual disability
Ying Weng, Xiaoping Luo, Ling Hou
P3-P263
A patient with Turner syndrome(45X/46XX) and Congenital Adrenal Hyperplasia
Yirou Wang, Yu Ding, Guoying Chang, Yao Chen, Yiping Shen, Xiumin Wang, Jian Wang
A patient with Turner syndrome(45X/46XX) and Congenital Adrenal Hyperplasia
Yirou Wang, Yu Ding, Guoying Chang, Yao Chen, Yiping Shen, Xiumin Wang, Jian Wang
P3-P264
Congenital tufting enteropathy caused by mutation of EPCAM gene: a case report and review of literature
yuan chuanjie, wu jing
Congenital tufting enteropathy caused by mutation of EPCAM gene: a case report and review of literature
yuan chuanjie, wu jing
P3-P401
Is using a specific growth charts a chance to be more precise in evaluation the growth of the children and adolescence with Down syndrome?Comparison of the Down`s syndrome growth charts with the growth charts for Polish population.
Ewa Barg, Marta Hetman
Is using a specific growth charts a chance to be more precise in evaluation the growth of the children and adolescence with Down syndrome?Comparison of the Down`s syndrome growth charts with the growth charts for Polish population.
Ewa Barg, Marta Hetman
P3-P406
Two siblings with Prader-Willi syndrome caused by microdeletion derived from the paternal grandmother
Guanping Dong, Yangli Dai, Ke Huang, Chaochun Zou, Xuefeng Chen
Two siblings with Prader-Willi syndrome caused by microdeletion derived from the paternal grandmother
Guanping Dong, Yangli Dai, Ke Huang, Chaochun Zou, Xuefeng Chen
P3-P415
Case Report: Novel ACAN mutation in a SGA short stature without accelerated skeletal maturation
So Eun Park, Ahn Sung Yeon
Case Report: Novel ACAN mutation in a SGA short stature without accelerated skeletal maturation
So Eun Park, Ahn Sung Yeon
RFC10.1
Patients with GH Insensitivity and IGF-1 Resistance Harbour Copy Number Variants Causing a Silver-Russell-Like Phenotype
Emily Cottrell, Sumana Chatterjee, Gudrun Moore, Miho Ishida, James Greening, Neil Wright, Artur Bossowski, Asma Deeb, Iman Al Basiri, Steven Rose, Avril Mason, Joowook Ahn, Susan Bint, Martin Savage, Louise A Metherell, Helen L Storr
Patients with GH Insensitivity and IGF-1 Resistance Harbour Copy Number Variants Causing a Silver-Russell-Like Phenotype
Emily Cottrell, Sumana Chatterjee, Gudrun Moore, Miho Ishida, James Greening, Neil Wright, Artur Bossowski, Asma Deeb, Iman Al Basiri, Steven Rose, Avril Mason, Joowook Ahn, Susan Bint, Martin Savage, Louise A Metherell, Helen L Storr
RFC15.1
Diagnosis of Silver-Russell syndrome in patients with chromosome 14q32.2 imprinted region disruption: phenotypic and molecular analysis
Sophie Geoffron, Walid Abi Habib, Sandra Chantot-Bastaraud, Madeleine Harbison, Jenifer Salem, Frédéric Brioude, Irène Netchine, Eloïse Giabicani
Diagnosis of Silver-Russell syndrome in patients with chromosome 14q32.2 imprinted region disruption: phenotypic and molecular analysis
Sophie Geoffron, Walid Abi Habib, Sandra Chantot-Bastaraud, Madeleine Harbison, Jenifer Salem, Frédéric Brioude, Irène Netchine, Eloïse Giabicani
RFC15.2
Molecular and clinical analyses of two UPD(16)mat patients detected by screening of 94 Silver-Russell syndrome patients without known etiology
Takanobu Inoue, Hideaki Yagasaki, Junko Nishioka, Akie Nakamura, Keiko Matsubara, Satoshi Narumi, Kazuhiko Nakabayashi, Kazuki Yamazawa, Tomoko Fuke, Akira Oka, Tsutomu Ogata, Maki Fukami, Masayo Kagami
Molecular and clinical analyses of two UPD(16)mat patients detected by screening of 94 Silver-Russell syndrome patients without known etiology
Takanobu Inoue, Hideaki Yagasaki, Junko Nishioka, Akie Nakamura, Keiko Matsubara, Satoshi Narumi, Kazuhiko Nakabayashi, Kazuki Yamazawa, Tomoko Fuke, Akira Oka, Tsutomu Ogata, Maki Fukami, Masayo Kagami
RFC15.3
Multiple pituitary hormone deficiencies and early onset obesity in two siblings with a mutation in the MAGEL2-gene.Evidence for an important regulatory function of the MAGEL2-gene in the hypothalamic-pituitary hormone pathways
Ursula Kuhnle-Krahl, Moneef Shoukier, Christian P. Schaaf, Cristoph Land
Multiple pituitary hormone deficiencies and early onset obesity in two siblings with a mutation in the MAGEL2-gene.Evidence for an important regulatory function of the MAGEL2-gene in the hypothalamic-pituitary hormone pathways
Ursula Kuhnle-Krahl, Moneef Shoukier, Christian P. Schaaf, Cristoph Land
RFC15.4
Characteristics, effectiveness and safety data from clinically relevant subgroups of patients with severeprimary IGF-I deficiency (SPIGFD): results from the European Increlex® Growth Forum Database (EU-IGFD) registry
Joachim Woelfle, Michel Polak, Valerie Perrot, Caroline Sert, Peter Bang
Characteristics, effectiveness and safety data from clinically relevant subgroups of patients with severeprimary IGF-I deficiency (SPIGFD): results from the European Increlex® Growth Forum Database (EU-IGFD) registry
Joachim Woelfle, Michel Polak, Valerie Perrot, Caroline Sert, Peter Bang
RFC15.5
Effect of Adjusting for Tanner Stage Age on Short and Tall Stature Prevalence in US Youths
O. Yaw Addo, Kyriakie Sarafoglou, Bradley Miller
Effect of Adjusting for Tanner Stage Age on Short and Tall Stature Prevalence in US Youths
O. Yaw Addo, Kyriakie Sarafoglou, Bradley Miller
RFC15.6
Latest results from PATRO Children, a multi-centre, non-interventional study of the long-term safety and efficacy of Omnitrope® in children requiring growth hormone treatment
Shankar Kanumakala, Roland Pfäffle, Charlotte Höybye, Berit Kriström, Tadej Battelino, Markus Zabransky, Hichem Zouater
Latest results from PATRO Children, a multi-centre, non-interventional study of the long-term safety and efficacy of Omnitrope® in children requiring growth hormone treatment
Shankar Kanumakala, Roland Pfäffle, Charlotte Höybye, Berit Kriström, Tadej Battelino, Markus Zabransky, Hichem Zouater
FC14.1
Awareness & participation in rare disease registries within the European Reference Network on Rare Endocrine Conditions (Endo-ERN)
Salma R. Ali, Jillian Bryce, Martine Cools, Marta Korbonits, Johan G. Beun, Domenica Taruscio, Felix Beuschlein, Thomas Danne, Mehul Dattani, Olaf Dekkers, Agnès Linglart, Irene Netchine, Anna Nordenstrom, Attila Patocs, Luca Persani, Arlene Smyth, Zdenek Sumnik, W. Edward Visser, Olaf Hiort, Alberto M. Pereira, S. Faisal Ahmed
Awareness & participation in rare disease registries within the European Reference Network on Rare Endocrine Conditions (Endo-ERN)
Salma R. Ali, Jillian Bryce, Martine Cools, Marta Korbonits, Johan G. Beun, Domenica Taruscio, Felix Beuschlein, Thomas Danne, Mehul Dattani, Olaf Dekkers, Agnès Linglart, Irene Netchine, Anna Nordenstrom, Attila Patocs, Luca Persani, Arlene Smyth, Zdenek Sumnik, W. Edward Visser, Olaf Hiort, Alberto M. Pereira, S. Faisal Ahmed
FC14.2
National UK guidelines for the clinical assessment, diagnosis, treatment and follow-up of children and young people (CYP) under 19 years of age with phaeochromocytoma (PCC) and paraganglioma (PGL) - On behalf of the UK Paediatric Phaeochromocytoma and Paraganglioma Guideline Development Group (GDG).
Harshini Katugampola, Stephen Marks, Samuel Quek, Prateek Yadav, Helen A. Spoudeas, Barney Harrison
National UK guidelines for the clinical assessment, diagnosis, treatment and follow-up of children and young people (CYP) under 19 years of age with phaeochromocytoma (PCC) and paraganglioma (PGL) - On behalf of the UK Paediatric Phaeochromocytoma and Paraganglioma Guideline Development Group (GDG).
Harshini Katugampola, Stephen Marks, Samuel Quek, Prateek Yadav, Helen A. Spoudeas, Barney Harrison
FC14.3
Regulation of salt, sugar and sex steroids in humans by genetic variations in NADPH Cytochrome P450 Oxidoreductase (POR) identified in 1000 genome samples
Amit V pandey av, Sameer S Udhane, Shaheena pARWEEN
Regulation of salt, sugar and sex steroids in humans by genetic variations in NADPH Cytochrome P450 Oxidoreductase (POR) identified in 1000 genome samples
Amit V pandey av, Sameer S Udhane, Shaheena pARWEEN
FC14.4
Glucocorticoid deficiency causes differentially dysregulated oxidative stress depending on the steroidogenic defects
Nan Li, Meltem Weger, Aliesha Griffin, Helen Eachus, Vincent T Cunliffe, Nils Krone
Glucocorticoid deficiency causes differentially dysregulated oxidative stress depending on the steroidogenic defects
Nan Li, Meltem Weger, Aliesha Griffin, Helen Eachus, Vincent T Cunliffe, Nils Krone
FC14.5
Pubertal females produce an enhanced interferon-alpha, anti-viral response compared to males, which is associated with X chromosome number, and not sex hormones
Kate Webb, Gary Butler, Coziana Ciurtin, Hannah Peckham, Anna Radziszewska, Lucy R Wedderburn, John Ioannou
Pubertal females produce an enhanced interferon-alpha, anti-viral response compared to males, which is associated with X chromosome number, and not sex hormones
Kate Webb, Gary Butler, Coziana Ciurtin, Hannah Peckham, Anna Radziszewska, Lucy R Wedderburn, John Ioannou
FC14.6
Sex differences in autoimmune disease: testosterone is associated with a decrease in expression of key anti-viral genes during puberty, which may decrease the risk of autoimmunity in males
Kate Webb, Gary Butler, Coziana Ciurtin, Hannah Peckham, Anna Radziszewska, Lucy R Wedderburn, Yiannis Ioannou
Sex differences in autoimmune disease: testosterone is associated with a decrease in expression of key anti-viral genes during puberty, which may decrease the risk of autoimmunity in males
Kate Webb, Gary Butler, Coziana Ciurtin, Hannah Peckham, Anna Radziszewska, Lucy R Wedderburn, Yiannis Ioannou
FC9.6
National UK guidelines for screening, multi-disciplinary team management and long-term follow-up of children and young people (CYP) with Multiple Endocrine Neoplasia Type 1 (MEN1).
Elizabeth Crowne, Rathi Prasad, Paul Newey, Karin Bradley, Richard Charnley, Helen Doran, Mark Callaway, Jonathan Mayhew, Brian Shine, Louise Izatt, Helen Spoudeas, Barney Harrison
National UK guidelines for screening, multi-disciplinary team management and long-term follow-up of children and young people (CYP) with Multiple Endocrine Neoplasia Type 1 (MEN1).
Elizabeth Crowne, Rathi Prasad, Paul Newey, Karin Bradley, Richard Charnley, Helen Doran, Mark Callaway, Jonathan Mayhew, Brian Shine, Louise Izatt, Helen Spoudeas, Barney Harrison
LB-P13
Clinical and endocrine characteristics and genetic analysis of Korean children with McCune–Albright syndrome
Eun-Kyung Cho, Minji Im, Jinsup Kim, Aram Yang, Ari Song, Chang-Seok Ki, Ji-Eun Lee, Sung Yoon Cho, Dong-Kyu Jin
Clinical and endocrine characteristics and genetic analysis of Korean children with McCune–Albright syndrome
Eun-Kyung Cho, Minji Im, Jinsup Kim, Aram Yang, Ari Song, Chang-Seok Ki, Ji-Eun Lee, Sung Yoon Cho, Dong-Kyu Jin
LB-P16
Successful treatment of Alopecia Totalis with calcitriol and paricalcitol in two girls aged 3 and 7-years
Dimitrios T. Papadimitriou, Christina Bothou, Eleni Dermitzaki, Kleanthis Kleanthous, Konstantinos Karkavitsas, George Mastorakos, Anastasios Papadimitriou
Successful treatment of Alopecia Totalis with calcitriol and paricalcitol in two girls aged 3 and 7-years
Dimitrios T. Papadimitriou, Christina Bothou, Eleni Dermitzaki, Kleanthis Kleanthous, Konstantinos Karkavitsas, George Mastorakos, Anastasios Papadimitriou
LB-P4
An updated evolutionary study in Glucocorticoid receptors; insights from a comprehensive phylogenetic, SNP’s and mutation’s analysis of the Nuclear receptors family.An updated evolutionary study in Glucocorticoid receptors; insights from a comprehensive phylogenetic, SNP’s and mutation’s analysis of the Nuclear receptors family.
Louis Papageorgiou, Eleni Papakonstantinou, Constantinos Salis, Sofia Raftopoulou, Thanasis Mitsis, Nicolas Nicolaides, Marianna Hagidimitriou, Elias Eliopoulos, Evangelia Charmandari, George Chrousos, Dimitrios Vlachakis
An updated evolutionary study in Glucocorticoid receptors; insights from a comprehensive phylogenetic, SNP’s and mutation’s analysis of the Nuclear receptors family.An updated evolutionary study in Glucocorticoid receptors; insights from a comprehensive phylogenetic, SNP’s and mutation’s analysis of the Nuclear receptors family.
Louis Papageorgiou, Eleni Papakonstantinou, Constantinos Salis, Sofia Raftopoulou, Thanasis Mitsis, Nicolas Nicolaides, Marianna Hagidimitriou, Elias Eliopoulos, Evangelia Charmandari, George Chrousos, Dimitrios Vlachakis
P1-P189
Clinical features and assessment of the pathway-care proposed by ISPED-Gsa Study Group in an Pediatric Italian cohort with Pseudohypoparathyroidism
Daniele Tessaris, Elisa Bonino, Patrizia Matarazzo, Gerdi Tuli, Malgorzata Wasniewska, Sandro Loche, Giovanna Weber, Luisa de Sanctis
Clinical features and assessment of the pathway-care proposed by ISPED-Gsa Study Group in an Pediatric Italian cohort with Pseudohypoparathyroidism
Daniele Tessaris, Elisa Bonino, Patrizia Matarazzo, Gerdi Tuli, Malgorzata Wasniewska, Sandro Loche, Giovanna Weber, Luisa de Sanctis
P1-P190
Overview of leading causes of death among French patients with Prader-Willi Syndrome, 2004-2014
Dibia Liz Pacoricona Alfaro, Perrine Lemoine, Catherine Molinas, Gwénaëlle Diene, Catherine Arnaud, Maithé Tauber
Overview of leading causes of death among French patients with Prader-Willi Syndrome, 2004-2014
Dibia Liz Pacoricona Alfaro, Perrine Lemoine, Catherine Molinas, Gwénaëlle Diene, Catherine Arnaud, Maithé Tauber
P1-P191
SGPL1 missense mutation in an infant with primary adrenal insufficiency (PAI), congenital nephrotic syndrome, primary hypothyroidism and gonadal failure
Avinaash Maharaj, Dean Wallace, Indi Banerjee, Rathi Prasad, Lou Metherell
SGPL1 missense mutation in an infant with primary adrenal insufficiency (PAI), congenital nephrotic syndrome, primary hypothyroidism and gonadal failure
Avinaash Maharaj, Dean Wallace, Indi Banerjee, Rathi Prasad, Lou Metherell
P1-P192
Final adult height, Insulin-like Growth Factor 1 (IGF-I) concentration in adolescents and young adults with β-thalassemia major (BTM) with and without Growth Hormone Deficiency
Ashraf Soliman, Mohamed Yassin, Vincenzo De Sanctis
Final adult height, Insulin-like Growth Factor 1 (IGF-I) concentration in adolescents and young adults with β-thalassemia major (BTM) with and without Growth Hormone Deficiency
Ashraf Soliman, Mohamed Yassin, Vincenzo De Sanctis
P1-P193
McCune-Albright-Syndrome: clinical and genetic study in a large cohort of pediatric patients.
Nadezhda Makazan, Elizaveta Orlova, Maria Kareva, Natalia Kalinchenko, Anna Kolodkina, Natalia Zubkova, Evgeniy Vasiliev, Anatoly Tiulpakov, Valentina Peterkova
McCune-Albright-Syndrome: clinical and genetic study in a large cohort of pediatric patients.
Nadezhda Makazan, Elizaveta Orlova, Maria Kareva, Natalia Kalinchenko, Anna Kolodkina, Natalia Zubkova, Evgeniy Vasiliev, Anatoly Tiulpakov, Valentina Peterkova
P2-P284
Endocrine and metabolic complications in children and adolescents with sickle cell disease: an Italian Cohort Study
Elena Bigi, Patrizia Bruzzi, Giovanni Palazzi, Barbara Predieri, Laura Lucaccioni, Alessia Pancaldi, Mariachiara Lodi, Monica Cellini, Lorenzo Iughetti
Endocrine and metabolic complications in children and adolescents with sickle cell disease: an Italian Cohort Study
Elena Bigi, Patrizia Bruzzi, Giovanni Palazzi, Barbara Predieri, Laura Lucaccioni, Alessia Pancaldi, Mariachiara Lodi, Monica Cellini, Lorenzo Iughetti
P2-P285
Bone marrow failure in McCune Albright Syndrome
Katja Wechsung, Erwin Lankes, Peter Kühnen, Arend von Stackelberg, Dirk Schnabel
Bone marrow failure in McCune Albright Syndrome
Katja Wechsung, Erwin Lankes, Peter Kühnen, Arend von Stackelberg, Dirk Schnabel
P2-P286
Final adult height, Insulin-like Growth Factor 1 (IGF-I) concentration and endocrine complications in adolescents and young adults with β-thalassemia major (BTM) who received oral iron chelation (OIC) in comparison with those who did not use OIC
Ashraf Soliman, Mohamed Yassin, Vincenzo De Sanctis
Final adult height, Insulin-like Growth Factor 1 (IGF-I) concentration and endocrine complications in adolescents and young adults with β-thalassemia major (BTM) who received oral iron chelation (OIC) in comparison with those who did not use OIC
Ashraf Soliman, Mohamed Yassin, Vincenzo De Sanctis
P2-P287
Endocrine challenges in patients with thalassemia
Tanja Christa Haamberg, Christine Schneider, Jochen Rössler, Christa E. Flück
Endocrine challenges in patients with thalassemia
Tanja Christa Haamberg, Christine Schneider, Jochen Rössler, Christa E. Flück
P2-P288
Can oral iron chelation therapies reduce endocrine complications in β-thalassemia major patients?
parastoo rostami, reyhaneh mohsenipour, mina khoshkbarforoshan, fatemeh sayarifard, arya setoudeh, alieh safari, farzad kompani
Can oral iron chelation therapies reduce endocrine complications in β-thalassemia major patients?
parastoo rostami, reyhaneh mohsenipour, mina khoshkbarforoshan, fatemeh sayarifard, arya setoudeh, alieh safari, farzad kompani
P2-P289
Statural growth and Endocrinopathies in relation to Liver Iron Content (LIC) and Insulin-Like Growth Factor 1 (IGF-I) concentration in adolescents with Beta Thalassemia Major (BTM) and Sickle Cell Disease (SCD)
AShraf Soliman, Mohamed Yassin, Vincenzo DE Sanctis, Abbas Moustafa, Sandra Abou Samaan, Abdulqadir Nashwan
Statural growth and Endocrinopathies in relation to Liver Iron Content (LIC) and Insulin-Like Growth Factor 1 (IGF-I) concentration in adolescents with Beta Thalassemia Major (BTM) and Sickle Cell Disease (SCD)
AShraf Soliman, Mohamed Yassin, Vincenzo DE Sanctis, Abbas Moustafa, Sandra Abou Samaan, Abdulqadir Nashwan
P2-P290
Successful treatment of severe atopic dermatitis with calcitriol and paricalcitol in an 8-year old girl
Christina Bothou, Alexis Alexopoulos, Eleni Dermitzaki, Kleanthis Kleanthous, Anastasios Papadimitriou, George Mastorakos, Dimitrios T. Papadimitriou
Successful treatment of severe atopic dermatitis with calcitriol and paricalcitol in an 8-year old girl
Christina Bothou, Alexis Alexopoulos, Eleni Dermitzaki, Kleanthis Kleanthous, Anastasios Papadimitriou, George Mastorakos, Dimitrios T. Papadimitriou
P2-P291
Hypoglycemia in adolescence as the presenting sign of familial MEN1
BAILLEUL Justine, BOUHOURS-NOUET Natacha, SUTEAU Valentine, AZGAL Maryam, CAMPAS Marie-Neige, DONZEAU Aurélie, COUTANT Régis
Hypoglycemia in adolescence as the presenting sign of familial MEN1
BAILLEUL Justine, BOUHOURS-NOUET Natacha, SUTEAU Valentine, AZGAL Maryam, CAMPAS Marie-Neige, DONZEAU Aurélie, COUTANT Régis
P2-P292
Aldosterone, renin, sodium and potassium excretion in normotensive prepubertal children
Alejandro Martinez-Aguyo, Helena Poggi, Carmen Campino, Soledad Peredo, René Baudrand, Cristian Carvajal, Ivonne D'Apremont, Rosario Moore, Sandra Solari, Fidel Allende, Carlos Fardella
Aldosterone, renin, sodium and potassium excretion in normotensive prepubertal children
Alejandro Martinez-Aguyo, Helena Poggi, Carmen Campino, Soledad Peredo, René Baudrand, Cristian Carvajal, Ivonne D'Apremont, Rosario Moore, Sandra Solari, Fidel Allende, Carlos Fardella
P2-P293
What is the impact of a structured Healthcare Pathway dedicated to patients in transition on their long-term follow-up?
Florence Menesguen, Isabelle Tejedor, Sabine Malivoir, Pauline Faucher, Marine Halbron, Marc Popelier, Juliane Leger, Irene Netchine, Michel Polak, Eric Bruckert, Christine Poitou, Philippe Touraine
What is the impact of a structured Healthcare Pathway dedicated to patients in transition on their long-term follow-up?
Florence Menesguen, Isabelle Tejedor, Sabine Malivoir, Pauline Faucher, Marine Halbron, Marc Popelier, Juliane Leger, Irene Netchine, Michel Polak, Eric Bruckert, Christine Poitou, Philippe Touraine
P2-P294
British Society for Paediatric Endocrinology and Diabetes peer review of specialised paediatric endocrinology services in the UK - evaluation of the process
John Schulga, Heather Mitchell, Pauline Musson, Nick Shaw, Leena Patel
British Society for Paediatric Endocrinology and Diabetes peer review of specialised paediatric endocrinology services in the UK - evaluation of the process
John Schulga, Heather Mitchell, Pauline Musson, Nick Shaw, Leena Patel
P2-P295
Paediatric Endocrinology mapping and services in Nigeria: a decade after
Iroro Yarhere, Tamunopriye Jaja
Paediatric Endocrinology mapping and services in Nigeria: a decade after
Iroro Yarhere, Tamunopriye Jaja
P2-P296
The impact of military conflict in the East of Ukraine on the physical development of children and adolescents
Svetlana Turchina, Tatyana Kostenko
The impact of military conflict in the East of Ukraine on the physical development of children and adolescents
Svetlana Turchina, Tatyana Kostenko
P2-P297
Polycystic Ovary syndrome Metabolic syndrome predisposition in puberty
STYLIANI GERONIKOLOU, FLORA BACOPOULOU, STAVROS CHRYSSANTHOPOULOS, DENNIS COKKINOS
Polycystic Ovary syndrome Metabolic syndrome predisposition in puberty
STYLIANI GERONIKOLOU, FLORA BACOPOULOU, STAVROS CHRYSSANTHOPOULOS, DENNIS COKKINOS
P2-P299
The N309K Pro-Protein Convertase Type 1 (PCSK1) Gene Mutation Causes Lack of Spontaneous Puberty and Primary Amenorrhea
Ulla Najwa Abdulhag, Mona Sharaf, Abdulsalam Abu Libdeh, David Zangen
The N309K Pro-Protein Convertase Type 1 (PCSK1) Gene Mutation Causes Lack of Spontaneous Puberty and Primary Amenorrhea
Ulla Najwa Abdulhag, Mona Sharaf, Abdulsalam Abu Libdeh, David Zangen
P2-P300
Somatostatin experiment in Prohormone Convertase Deficiency
Ödül Eğritaş, Aylin Kılınç Uğurlu, esra döğer, Emine Demet Akbaş, Aysun Bideci, Buket Dalgıç, Orhun Çamurdan, Peyami Cinaz
Somatostatin experiment in Prohormone Convertase Deficiency
Ödül Eğritaş, Aylin Kılınç Uğurlu, esra döğer, Emine Demet Akbaş, Aysun Bideci, Buket Dalgıç, Orhun Çamurdan, Peyami Cinaz
P3-P265
Insulinoma as initial presentation of Multiple Endocrine Neoplasia type 1
Ada Borowiec, Anna Kucharska, Beata Pyrżak
Insulinoma as initial presentation of Multiple Endocrine Neoplasia type 1
Ada Borowiec, Anna Kucharska, Beata Pyrżak
P3-P266
Assessment of ovarian reserve in young women with Hashimoto disease - the pilot study
Anna Wedrychowicz, Joanna Wojtyś, Malgorzata Stelmach, Jerzy B. Starzyk
Assessment of ovarian reserve in young women with Hashimoto disease - the pilot study
Anna Wedrychowicz, Joanna Wojtyś, Malgorzata Stelmach, Jerzy B. Starzyk
P3-P267
Unusual clinical presentation of autoimmune polyendocrinopathy type 1
Federico Baronio, Rita Ortolano, Simona Ferrari, Alessandra Cassio, Giulio Maltoni, Giacomo Tonti, Antonio Balsamo
Unusual clinical presentation of autoimmune polyendocrinopathy type 1
Federico Baronio, Rita Ortolano, Simona Ferrari, Alessandra Cassio, Giulio Maltoni, Giacomo Tonti, Antonio Balsamo
P3-P268
Glycemic abnormalities and normal thyroid function in adolescent survivors of childhood acute lymphocytic leukemia who required repeated packed red cell transfusion during treatment
ASHRAF SOLIMAN, Mohamed Yassin
Glycemic abnormalities and normal thyroid function in adolescent survivors of childhood acute lymphocytic leukemia who required repeated packed red cell transfusion during treatment
ASHRAF SOLIMAN, Mohamed Yassin
P3-P269
Graves’ disease in children with T1DM: a report of three cases
Can Thi Bich Ngoc, Vu Chi Dung, Bui Phuong Thao, Nguyen Ngoc Khanh, Nguyen Thu Ha, Nguyen Phu Dat
Graves’ disease in children with T1DM: a report of three cases
Can Thi Bich Ngoc, Vu Chi Dung, Bui Phuong Thao, Nguyen Ngoc Khanh, Nguyen Thu Ha, Nguyen Phu Dat
P3-P270
Case report: Neonatal McCune-Albright syndrome with juvenile ovarian granulosa cell tumor in a 4 months old girl
Esther Schulz, Stephan Klohs, Ingo Königs, Thomas Maiberger, Johanna Nissen, Hansjörg Schäfer, Wolfgang Saeger, Clivia Schnegg, Thomas Mir, Rainer Gerhard Kozlik-Feldmann, Ilker Akkurt
Case report: Neonatal McCune-Albright syndrome with juvenile ovarian granulosa cell tumor in a 4 months old girl
Esther Schulz, Stephan Klohs, Ingo Königs, Thomas Maiberger, Johanna Nissen, Hansjörg Schäfer, Wolfgang Saeger, Clivia Schnegg, Thomas Mir, Rainer Gerhard Kozlik-Feldmann, Ilker Akkurt
P3-P271
Polyostotic Fibrous Dysplasia of McCune Albright Syndrome responding to intravenous Zoledronate therapy
Ganesh H K, Girisha K M
Polyostotic Fibrous Dysplasia of McCune Albright Syndrome responding to intravenous Zoledronate therapy
Ganesh H K, Girisha K M
P3-P272
Two cases of Costello Syndrome and literatures review
Jiang Zhuan-nan, Hou Le-le, Liu Zu-lin, Ou Hui, Meng Zhe, Zhang Li-na, Liang Li-yang
Two cases of Costello Syndrome and literatures review
Jiang Zhuan-nan, Hou Le-le, Liu Zu-lin, Ou Hui, Meng Zhe, Zhang Li-na, Liang Li-yang
P3-P273
ENDOCRINE COMPLICATIONS IN BETA-THALASSAEMIA MAJOR CHILDREN
Mirela Elena Iancu, Alice Ioana Albu
ENDOCRINE COMPLICATIONS IN BETA-THALASSAEMIA MAJOR CHILDREN
Mirela Elena Iancu, Alice Ioana Albu
P3-P274
The case of combination of multinodular goiter and Sertoli-Leydig cell ovarian tumor due to mutation in DICER1 gene
Anna Kolodkina, Nina Makretskaya, Anatoly Tiulpakov
The case of combination of multinodular goiter and Sertoli-Leydig cell ovarian tumor due to mutation in DICER1 gene
Anna Kolodkina, Nina Makretskaya, Anatoly Tiulpakov
P3-P276
Autoimmunepolyendocrinopathy-Candidiasis-Ectodermal Dystrophy: a Case Report
Tanju Celik, Ozlem Nalbantoglu, Semra Gursoy, Ozlem Sangun, Gulcin Arslan, Behzat Ozkan
Autoimmunepolyendocrinopathy-Candidiasis-Ectodermal Dystrophy: a Case Report
Tanju Celik, Ozlem Nalbantoglu, Semra Gursoy, Ozlem Sangun, Gulcin Arslan, Behzat Ozkan
P3-P277
WOLMAN DISEASE: LONG-TERM ENDOCRINE AND METABOLIC COMORBIDITIES
Rachel Bello, Jerry Stein, Moshe Phillip, Shlomit Shalitin
WOLMAN DISEASE: LONG-TERM ENDOCRINE AND METABOLIC COMORBIDITIES
Rachel Bello, Jerry Stein, Moshe Phillip, Shlomit Shalitin
P3-P278
Pallister Hall Syndrome: with a varied spectrum of endocrine disorders
Smita Ramachandran, Aashish Sethi, Inderpal Kochar
Pallister Hall Syndrome: with a varied spectrum of endocrine disorders
Smita Ramachandran, Aashish Sethi, Inderpal Kochar
P3-P279
Near electromagnetic fields - induced syndrome: unsuspected and newly recognised
STYLIANI GERONIKOLOU, GEORGE CHROUSOS, CHRISTINA KANAKA-GANTENBEIN
Near electromagnetic fields - induced syndrome: unsuspected and newly recognised
STYLIANI GERONIKOLOU, GEORGE CHROUSOS, CHRISTINA KANAKA-GANTENBEIN
P3-P280
Polycystic Ovary syndrome gene/gene products interaction network
STYLIANI GERONIKOLOU, ATHANASSIA PAVLOPOULOU, DENNIS COKKINOS, CHRISTINA KANAKA-GANTENBEIN, FLORA BACOPOULOU
Polycystic Ovary syndrome gene/gene products interaction network
STYLIANI GERONIKOLOU, ATHANASSIA PAVLOPOULOU, DENNIS COKKINOS, CHRISTINA KANAKA-GANTENBEIN, FLORA BACOPOULOU
P3-P281
Basal metabolic rate as moderator of inflammation in PCOS
STYLIANI GERONIKOLOU, DENNIS COKKINOS, FLORA BACOPOULOU
Basal metabolic rate as moderator of inflammation in PCOS
STYLIANI GERONIKOLOU, DENNIS COKKINOS, FLORA BACOPOULOU
P3-P282
Insight of differential diagnosis of DAX-1 from two patients with elevated testosterone in early infancy
Tang Li, Juan Ge
Insight of differential diagnosis of DAX-1 from two patients with elevated testosterone in early infancy
Tang Li, Juan Ge
P3-P283
Rapid onset and progression of chronic kidney disease in a child with Autoimmune Polyglandular Syndrome Type 1
Vasiliki Rengina Tsinopoulou, Eleni P Kotanidou, Maria Grammatiki, Styliani Giza, Tasos Tzirtzipis, Olga Nikolaidou, Eleni Litou, Theodoros Liarogkovinos, Despina Tramma, Panagiotis Pateinakis, Dorothea Papadopoulou, Assimina Galli-Tsinopoulou
Rapid onset and progression of chronic kidney disease in a child with Autoimmune Polyglandular Syndrome Type 1
Vasiliki Rengina Tsinopoulou, Eleni P Kotanidou, Maria Grammatiki, Styliani Giza, Tasos Tzirtzipis, Olga Nikolaidou, Eleni Litou, Theodoros Liarogkovinos, Despina Tramma, Panagiotis Pateinakis, Dorothea Papadopoulou, Assimina Galli-Tsinopoulou
P3-P402
Clinical characteristics and outcome of patients with beta-ketothiolase deficiency in China
yang lili
Clinical characteristics and outcome of patients with beta-ketothiolase deficiency in China
yang lili
P3-P405
Lessons from Wolfram Syndrome: Initiation of DDAVP therapy causes Renal Salt Wasting due to elevated ANP levels, rescued by fludrocortisone treatment.
Kleanthis Kleanthous, Eirini Maratou, Dora Spyropoulou, Eleni Dermitzaki, Christina Bothou, Anastasios Papadimitriou, George Zoupanos, Paraskevi Moutsatsou, Fumihiko Urano, Dimitrios T. Papadimitriou
Lessons from Wolfram Syndrome: Initiation of DDAVP therapy causes Renal Salt Wasting due to elevated ANP levels, rescued by fludrocortisone treatment.
Kleanthis Kleanthous, Eirini Maratou, Dora Spyropoulou, Eleni Dermitzaki, Christina Bothou, Anastasios Papadimitriou, George Zoupanos, Paraskevi Moutsatsou, Fumihiko Urano, Dimitrios T. Papadimitriou
P3-P410
A novel detrimental homozygous mutation of WFS1 gene in two sisters from non-consanguineous parents with untreated Diabetes Insipidus
Dimitrios T. Papadimitriou, Kleanthis Kleanthous, Emmanouil Manolakos, Anatoly Tiulpakov, Thomas Nikolopoulos, Alexandros Delides, Gerasimos Voros, Argyrios Dinopoulos, George Zoupanos, Fumihiko Urano
A novel detrimental homozygous mutation of WFS1 gene in two sisters from non-consanguineous parents with untreated Diabetes Insipidus
Dimitrios T. Papadimitriou, Kleanthis Kleanthous, Emmanouil Manolakos, Anatoly Tiulpakov, Thomas Nikolopoulos, Alexandros Delides, Gerasimos Voros, Argyrios Dinopoulos, George Zoupanos, Fumihiko Urano
P3-P411
General public’ attitudes towards the use and storage of NBS blood samples for research in China
yang lili
General public’ attitudes towards the use and storage of NBS blood samples for research in China
yang lili
RFC14.1
Psychometric and Psycho-social Profile of Children and Adolescent Survivors of Pediatric Cancer
Flora Bacopoulou, Kalliopi Mavrea, Christina Adamaki, Vasiliki Efthymiou, Katerina Katsibardi, Antonis Kattamis
Psychometric and Psycho-social Profile of Children and Adolescent Survivors of Pediatric Cancer
Flora Bacopoulou, Kalliopi Mavrea, Christina Adamaki, Vasiliki Efthymiou, Katerina Katsibardi, Antonis Kattamis
RFC14.2
British Society for Paediatric Endocrinology and Diabetes peer review of specialised paediatric endocrinology services in the UK - evaluation of the outcomes
Joihn Schulga, Heather Mitchell, Pauline Musson, Nick Shaw, Leena Patel
British Society for Paediatric Endocrinology and Diabetes peer review of specialised paediatric endocrinology services in the UK - evaluation of the outcomes
Joihn Schulga, Heather Mitchell, Pauline Musson, Nick Shaw, Leena Patel
RFC14.3
Dysregulated glucose homeostasis in Congenital Central Hypoventilation Syndrome
Yassmin Musthaffa, Vikash Goyal, Margaret-Anne Harris, Nitin Kapur, Juliane Leger, Mark Harris
Dysregulated glucose homeostasis in Congenital Central Hypoventilation Syndrome
Yassmin Musthaffa, Vikash Goyal, Margaret-Anne Harris, Nitin Kapur, Juliane Leger, Mark Harris
RFC14.4
A novel germline DICER1 mutation in a girl with multinodular goiter and ovarian Sertoli-Leydig cell tumor
Nikolaos Settas, Lina Michala, Annabel Berthon, Fabio Faucz, Alexandra Iliadi, Anna Gkika, Catherine Dacou-Voutetakis, Constantine Stratakis, Antonis Voutetakis
A novel germline DICER1 mutation in a girl with multinodular goiter and ovarian Sertoli-Leydig cell tumor
Nikolaos Settas, Lina Michala, Annabel Berthon, Fabio Faucz, Alexandra Iliadi, Anna Gkika, Catherine Dacou-Voutetakis, Constantine Stratakis, Antonis Voutetakis
RFC14.5
Natural course of MEN type 2B syndrome; a Dutch single-center cohort.
Ester Rijks, Gerlof Valk, Annemarie Verrijn Stuart
Natural course of MEN type 2B syndrome; a Dutch single-center cohort.
Ester Rijks, Gerlof Valk, Annemarie Verrijn Stuart
RFC14.6
Identification of epithelial sodium channel (ENaC) in endometrial pipelle biopsy samples
Vijay Boggula, Israel Hanukoglu, Ron Sagiv, Yehoshua Enuka, Aaron Hanukoglu
Identification of epithelial sodium channel (ENaC) in endometrial pipelle biopsy samples
Vijay Boggula, Israel Hanukoglu, Ron Sagiv, Yehoshua Enuka, Aaron Hanukoglu
FC5.1
Beta1-Tubulin gene (TUBB1) mutations cause thyroid dysgenesis associated to abnormal platelet morphology and hyper-aggregation
Aurore Carré, Athanasia Stoupa, Frédéric Adam, Dulanjalee Kariyawasam, Catherine Strassel, Sanjay Gawade, Gabor Szinnai, Alexandre Kauskot, Dominique Lasne, Carsten Janke, Kathiresan Natarajan, Alain Schmitt, Christine Bole-Feysot, Patrick Nitschke, Juliane Léger, Fabienne Jabot-Hanin, Frédéric Tores, Anita Michel, Arnold Munnich, Claude Besmond, Raphaël Scharfmann, François Lanza, Delphine Borgel, Michel Polak, Fédération Parisienne pour le Dépistage et la Prévention des Handicaps de l’Enfant FPDPHE
Beta1-Tubulin gene (TUBB1) mutations cause thyroid dysgenesis associated to abnormal platelet morphology and hyper-aggregation
Aurore Carré, Athanasia Stoupa, Frédéric Adam, Dulanjalee Kariyawasam, Catherine Strassel, Sanjay Gawade, Gabor Szinnai, Alexandre Kauskot, Dominique Lasne, Carsten Janke, Kathiresan Natarajan, Alain Schmitt, Christine Bole-Feysot, Patrick Nitschke, Juliane Léger, Fabienne Jabot-Hanin, Frédéric Tores, Anita Michel, Arnold Munnich, Claude Besmond, Raphaël Scharfmann, François Lanza, Delphine Borgel, Michel Polak, Fédération Parisienne pour le Dépistage et la Prévention des Handicaps de l’Enfant FPDPHE
FC5.2
Enrichment of inherited rare variants in non-syndromic congenital hypothyroidism from thyroid dysgenesis identified by exome sequencing: the contribution of IKBKE to vasculogenesis and thyroid development
Stéphanie Larrivée-Vanier, Fabien Magne, Martineau Jean-Louis, Aurore Carré, Helen Bui, Mark E. Samuels, Michel Polak, Guy Van Vliet, Johnny Deladoëy
Enrichment of inherited rare variants in non-syndromic congenital hypothyroidism from thyroid dysgenesis identified by exome sequencing: the contribution of IKBKE to vasculogenesis and thyroid development
Stéphanie Larrivée-Vanier, Fabien Magne, Martineau Jean-Louis, Aurore Carré, Helen Bui, Mark E. Samuels, Michel Polak, Guy Van Vliet, Johnny Deladoëy
FC5.3
Computational analysis of the ligand binding domain of the thyroid hormone receptor for the rational design of an efficient protein-based biosensor for the detection of thyroid hormone disrupting chemicals
Sonia Verma, Amit V Pandey
Computational analysis of the ligand binding domain of the thyroid hormone receptor for the rational design of an efficient protein-based biosensor for the detection of thyroid hormone disrupting chemicals
Sonia Verma, Amit V Pandey
FC5.4
Thyroid hormone analog therapy in patients with MCT8 deficiency: the Triac Trial
Stefan Groeneweg, René de Coo, Ingrid van Beynum, Marieke van der Knoop, Femke Aarsen, Yolanda de Rijke, Robin Peeters, Theo Visser, Edward Visser
Thyroid hormone analog therapy in patients with MCT8 deficiency: the Triac Trial
Stefan Groeneweg, René de Coo, Ingrid van Beynum, Marieke van der Knoop, Femke Aarsen, Yolanda de Rijke, Robin Peeters, Theo Visser, Edward Visser
FC5.5
Guidelines for the management of Paediatric Differentiated Thyroid Carcinoma; a UK endeavour
Sasha Howard, Kate Newbold, Sarah Freeston, Sonali Natu, Sabine Pomplun, Louise Izatt, Mark Gaze, Harrison Barney, Helen Spoudeas, Sophie Wilne
Guidelines for the management of Paediatric Differentiated Thyroid Carcinoma; a UK endeavour
Sasha Howard, Kate Newbold, Sarah Freeston, Sonali Natu, Sabine Pomplun, Louise Izatt, Mark Gaze, Harrison Barney, Helen Spoudeas, Sophie Wilne
FC5.6
Alterations in DNA methylation status of gene promoters in children and adolescents with autoimmune thyroid disease
Ioannis Kyrgios, Aikaterini Fragkou, Smaragda Efraimidou, Georgios Tzimagiorgis, Maria Emporiadou-Petikopoulou, Assimina Galli-Tsinopoulou
Alterations in DNA methylation status of gene promoters in children and adolescents with autoimmune thyroid disease
Ioannis Kyrgios, Aikaterini Fragkou, Smaragda Efraimidou, Georgios Tzimagiorgis, Maria Emporiadou-Petikopoulou, Assimina Galli-Tsinopoulou
FC7.5
Thyroid hormone levels in cord blood are associated with fetal and neonatal growth
Malene K. Hansen, Nina Strandkjær, Ruth Frikke-Schmidt, Henning Bundgaard, Katharina M. Main, Kasper K. Iversen
Thyroid hormone levels in cord blood are associated with fetal and neonatal growth
Malene K. Hansen, Nina Strandkjær, Ruth Frikke-Schmidt, Henning Bundgaard, Katharina M. Main, Kasper K. Iversen
FC7.6
TSH-resistance and remaining low-T4 in former low-birthweight infants – a study in monozygotic twins with intra-twin birth-weight-differences
Sandra Schulte, Joachim Woelfle, Peter Bartmann, Felix Schreiner, Evangelia Panou, Heike Vollbach, Bettina Gohlke
TSH-resistance and remaining low-T4 in former low-birthweight infants – a study in monozygotic twins with intra-twin birth-weight-differences
Sandra Schulte, Joachim Woelfle, Peter Bartmann, Felix Schreiner, Evangelia Panou, Heike Vollbach, Bettina Gohlke
LB-P10
The influence of oil-soluble iodinated contrast medium (Lipiodol) on child’s thyroid function in mice
Tadashi Hongyo, Masahiro Namise, Yukimitsu Sawai, Io Ishibashi, Hirofumi Kuchino, Itsuki Seki, Shota Hirose, Kentaro Yamamura, Yasuyuki Ueda
The influence of oil-soluble iodinated contrast medium (Lipiodol) on child’s thyroid function in mice
Tadashi Hongyo, Masahiro Namise, Yukimitsu Sawai, Io Ishibashi, Hirofumi Kuchino, Itsuki Seki, Shota Hirose, Kentaro Yamamura, Yasuyuki Ueda
P1-P248
Early determinants of thyroid function outcome in children with congenital hypothyroidism and a normally located thyroid gland: a regional cohort study
Carole Saba, Sophie Guilmin-Crepon, Delphine Zénaty, Laetitia Martinerie, Anne Paulsen, Dominique Simon, Sophie Dos Santos, Jeremy Haignere, Damir Mohamed, Carel Jean-Claude, Léger Juliane
Early determinants of thyroid function outcome in children with congenital hypothyroidism and a normally located thyroid gland: a regional cohort study
Carole Saba, Sophie Guilmin-Crepon, Delphine Zénaty, Laetitia Martinerie, Anne Paulsen, Dominique Simon, Sophie Dos Santos, Jeremy Haignere, Damir Mohamed, Carel Jean-Claude, Léger Juliane
P1-P249
Neonatal screening for congenital hypothyroidism: age-dependent reference intervals for dried blood spot TSH in the neonatal period
Carlo Corbetta, Simona De Angelis, Daniela Rotondi, Luisella Alberti, Pamela Cassini, Tiziana Mariani, Silvana Caiulo, Maria Cristina Vigone, Giovanna Weber, Antonella Olivieri
Neonatal screening for congenital hypothyroidism: age-dependent reference intervals for dried blood spot TSH in the neonatal period
Carlo Corbetta, Simona De Angelis, Daniela Rotondi, Luisella Alberti, Pamela Cassini, Tiziana Mariani, Silvana Caiulo, Maria Cristina Vigone, Giovanna Weber, Antonella Olivieri
P1-P250
Thyroid scintigraphy in the diagnosis of Congenital Hypothyroidism
Chris Woth, Indi Banerjee, Beverley Hird, Leena Patel, Lesley Tetlow
Thyroid scintigraphy in the diagnosis of Congenital Hypothyroidism
Chris Woth, Indi Banerjee, Beverley Hird, Leena Patel, Lesley Tetlow
P1-P251
Congenital hypothyroidism (CH) with delayed TSH elevation: the importance of the second-screening strategy and the evolution of CH in preterm infants
Silvana Caiulo, Maria Cristina Vigone, Antonella Olivieri, Marianna di Frenna, Gaia Vincenzi, Graziano Barera, Carlo Corbetta, Giovanna Weber
Congenital hypothyroidism (CH) with delayed TSH elevation: the importance of the second-screening strategy and the evolution of CH in preterm infants
Silvana Caiulo, Maria Cristina Vigone, Antonella Olivieri, Marianna di Frenna, Gaia Vincenzi, Graziano Barera, Carlo Corbetta, Giovanna Weber
P1-P252
Morning versus bedtime Levothyroxine administration: what is the choice of children?
ONUR AKIN
Morning versus bedtime Levothyroxine administration: what is the choice of children?
ONUR AKIN
P1-P253
Long term comparison between liquid and tablet formulations of L-Thyroxine (L-T4) in the treatment of Congenital Hypothyroidism (CH)
Maria Cristina Vigone, Rita Ortolano, Gaia Vincenzi, Clara Pozzi, Micol Ratti, Valentina Assirelli, Sofia Vissani, Paolo Cavarzere, Alessandro Mussa, ROberto Gastaldi, Raffaella Di Mase, Maria Elisabeth Street, Jessica Trombatore, Giovanna Weber, Alessandra Cassio
Long term comparison between liquid and tablet formulations of L-Thyroxine (L-T4) in the treatment of Congenital Hypothyroidism (CH)
Maria Cristina Vigone, Rita Ortolano, Gaia Vincenzi, Clara Pozzi, Micol Ratti, Valentina Assirelli, Sofia Vissani, Paolo Cavarzere, Alessandro Mussa, ROberto Gastaldi, Raffaella Di Mase, Maria Elisabeth Street, Jessica Trombatore, Giovanna Weber, Alessandra Cassio
P1-P254
Isolated Congenital Central Hypothyroidism due to a novel mutation in TSH beta subunit gene
Tarik Kirkgoz, Bayram Ozhan, Ozan Cetin, Sare Betul Kaygusuz, Serap Turan, Abdullah Bereket, Tulay Guran
Isolated Congenital Central Hypothyroidism due to a novel mutation in TSH beta subunit gene
Tarik Kirkgoz, Bayram Ozhan, Ozan Cetin, Sare Betul Kaygusuz, Serap Turan, Abdullah Bereket, Tulay Guran
P1-P255
Patterns of thyroglobulin levels in infants referred with high TSH on newborn screening, compared with iodine-sufficient healthy controls
Wafa Kallali, David Neumann, Kateřina Krylová, Jeremy H. Jones, Karen Smith, Guftar Shaikh, Malcolm Donaldson
Patterns of thyroglobulin levels in infants referred with high TSH on newborn screening, compared with iodine-sufficient healthy controls
Wafa Kallali, David Neumann, Kateřina Krylová, Jeremy H. Jones, Karen Smith, Guftar Shaikh, Malcolm Donaldson
P1-P256
Mutation screening in 60 Chinese patients with congenital hypothyroidism
Zhangqian Zheng, Wei Lu, Jing Wu, Feihong Luo
Mutation screening in 60 Chinese patients with congenital hypothyroidism
Zhangqian Zheng, Wei Lu, Jing Wu, Feihong Luo
P1-P257
Results of the hTPO mutational screening in Bulgarian patients with congenital hypothyroidism (CH)
Iva Stoeva, Kalina Mihova, Boris Stoilov, Reni Koleva, Wilhelm Mladenov, Violeta Iotova, Radka Kaneva
Results of the hTPO mutational screening in Bulgarian patients with congenital hypothyroidism (CH)
Iva Stoeva, Kalina Mihova, Boris Stoilov, Reni Koleva, Wilhelm Mladenov, Violeta Iotova, Radka Kaneva
P1-P258
Thyroid Hormone Resistance Beta: Eighteen Pediatric Patient Experience
Ulku Gul Siraz, Gul Direk, Leyla Akin, Rıfat Bircan, Zeynep Uzan Tatli, Nihal Hatipoglu, Mustafa Kendirci, Selim Kurtoglu
Thyroid Hormone Resistance Beta: Eighteen Pediatric Patient Experience
Ulku Gul Siraz, Gul Direk, Leyla Akin, Rıfat Bircan, Zeynep Uzan Tatli, Nihal Hatipoglu, Mustafa Kendirci, Selim Kurtoglu
P1-P260
Multinodular goiter in childhood: a diagnostic gateway for screening DICER1 syndrome
Isabelle OLIVER PETIT, Solange Grunenwald, Lisa Golmard, frédérique Savagner
Multinodular goiter in childhood: a diagnostic gateway for screening DICER1 syndrome
Isabelle OLIVER PETIT, Solange Grunenwald, Lisa Golmard, frédérique Savagner
P1-P261
A novel DICER1 mutation identified in a family with the multinodular goiter of children
Keisuke Nagasaki, Nao Shibata, Hiromi Nyuzuki, Sunao Sasaki, Yohei Ogawa, Takahiko Kogai, Akira Hishinuma
A novel DICER1 mutation identified in a family with the multinodular goiter of children
Keisuke Nagasaki, Nao Shibata, Hiromi Nyuzuki, Sunao Sasaki, Yohei Ogawa, Takahiko Kogai, Akira Hishinuma
P1-P262
Subclinical hypothyroidism, thyroid nodule or cyst in prepubertal children: how many children were diagnosed at age 6?
Young Ah Lee, Sun Wook Cho, Youn-Hee Lim, Johanna Inhyang Kim, Bung-Nyun Kim, Yun-Chul Hong, Young Joo Park, Choong Ho Shin, Sei Won Yang
Subclinical hypothyroidism, thyroid nodule or cyst in prepubertal children: how many children were diagnosed at age 6?
Young Ah Lee, Sun Wook Cho, Youn-Hee Lim, Johanna Inhyang Kim, Bung-Nyun Kim, Yun-Chul Hong, Young Joo Park, Choong Ho Shin, Sei Won Yang
P1-P263
Expression of ZnT8 transporter in thyroid tissues from patients with immune and non-immune thyroid diseases
Artur Bossowski, Joanna Reszec, Dariusz Polnik, Marta Gasowska, Wieslawa Niklinska
Expression of ZnT8 transporter in thyroid tissues from patients with immune and non-immune thyroid diseases
Artur Bossowski, Joanna Reszec, Dariusz Polnik, Marta Gasowska, Wieslawa Niklinska
P1-P264
Thyroid nodules in a childhood cancers survivors population: a monocentric experience.
Emanuela Peschiaroli, Graziamaria Ubertini, Armando Grossi, Giusy Ferro, Ludovica Martini, Laura Paone, Maria Debora De Pasquale, Barbara Baldini Ferroli, Marco Cappa
Thyroid nodules in a childhood cancers survivors population: a monocentric experience.
Emanuela Peschiaroli, Graziamaria Ubertini, Armando Grossi, Giusy Ferro, Ludovica Martini, Laura Paone, Maria Debora De Pasquale, Barbara Baldini Ferroli, Marco Cappa
P1-P265
HLA alleles and amino acid variants of HLA-A, -B, -C, -DRB1, -DQB1, -DPB1 molecules in early-onset autoimmune thyroid disease
Won Kyoung Cho, Dong Hwan Shin, Seul Ki Kim, Seonhwa Lee, Yujung Choi, Moonbae Ahn, In Cheol Baek, Min Ho Jung, Tai-Gyu Kim, Byung-Kyu Suh
HLA alleles and amino acid variants of HLA-A, -B, -C, -DRB1, -DQB1, -DPB1 molecules in early-onset autoimmune thyroid disease
Won Kyoung Cho, Dong Hwan Shin, Seul Ki Kim, Seonhwa Lee, Yujung Choi, Moonbae Ahn, In Cheol Baek, Min Ho Jung, Tai-Gyu Kim, Byung-Kyu Suh
P1-P266
Childhood thyroid autoimmunity and relation to islet autoantibodies in children at risk for Type 1 Diabetes
Berglind Jonsdottir, Christer Larsson, Ida Jönsson, Markus Lundgren, Helena Larsson
Childhood thyroid autoimmunity and relation to islet autoantibodies in children at risk for Type 1 Diabetes
Berglind Jonsdottir, Christer Larsson, Ida Jönsson, Markus Lundgren, Helena Larsson
P1-P267
Evaluation of serum concentrations of selected cytokines OPG and sRANKL in the diagnosis of autoimmune thyroid disease in children
Hanna Mikos, Marcin Mikos, Marek Niedziela
Evaluation of serum concentrations of selected cytokines OPG and sRANKL in the diagnosis of autoimmune thyroid disease in children
Hanna Mikos, Marcin Mikos, Marek Niedziela
P1-P268
Analysis of zinc- transporter ZnT8 autoantibodies in children and adolescents with autoimmune thyroid diseases
Justyna Michalak, Marta Rydzewska, Artur Bossowski
Analysis of zinc- transporter ZnT8 autoantibodies in children and adolescents with autoimmune thyroid diseases
Justyna Michalak, Marta Rydzewska, Artur Bossowski
P1-P269
The association between TSHR, IFIH1 and ETV5 polymorphisms with Graves’ disease and Diabetes Mellitus Type 1 in children
Karolina Stozek, Natalia Wawrusiewicz-Kurylonek, Joanna Goscik, Malgorzata Wasniewska, Tommaso Aversa, Domenico Corica, Adam Kretowski, Artur Bossowski
The association between TSHR, IFIH1 and ETV5 polymorphisms with Graves’ disease and Diabetes Mellitus Type 1 in children
Karolina Stozek, Natalia Wawrusiewicz-Kurylonek, Joanna Goscik, Malgorzata Wasniewska, Tommaso Aversa, Domenico Corica, Adam Kretowski, Artur Bossowski
P2-P376
Long term monitoring of Graves Disease in children and adolescents: single center experience
Selma Tunç, Özge Köprülü, Hatice Ortaç, Özlem Nalbantoğlu, Ceyhun Dizdarer, Korcan Demir, Behzat Özkan
Long term monitoring of Graves Disease in children and adolescents: single center experience
Selma Tunç, Özge Köprülü, Hatice Ortaç, Özlem Nalbantoğlu, Ceyhun Dizdarer, Korcan Demir, Behzat Özkan
P2-P377
Effects of Thyroid Autoimmunity on Non-Alcoholic Fatty Liver Disease in Euthyroid Girls with Hashimoto’s Thyroiditis
Pınar İşgüven, Dilek Ersavaş, Mehmet Ersavaş, Bahri Elmas
Effects of Thyroid Autoimmunity on Non-Alcoholic Fatty Liver Disease in Euthyroid Girls with Hashimoto’s Thyroiditis
Pınar İşgüven, Dilek Ersavaş, Mehmet Ersavaş, Bahri Elmas
P2-P378
The prevalence of clinically significant anti-TPO positivity in children with HLA-conferred susceptibility to Type 1 Diabetes
Liisa Saare, Aleksandr Peet, Vallo Tillmann
The prevalence of clinically significant anti-TPO positivity in children with HLA-conferred susceptibility to Type 1 Diabetes
Liisa Saare, Aleksandr Peet, Vallo Tillmann
P2-P379
Encephalopathy associated with Autoimmune Thyroid Disease: a case report
Hector Lantigua, Michael Yafi
Encephalopathy associated with Autoimmune Thyroid Disease: a case report
Hector Lantigua, Michael Yafi
P2-P380
Celiac disease screening should be routinely offered in pediatric population with autoimmune thyroid disease
Maria Resta, Panagiota Triantafyllou, Charalampos Agakidis, Olga Maliachova, Athanasios Christoforidis
Celiac disease screening should be routinely offered in pediatric population with autoimmune thyroid disease
Maria Resta, Panagiota Triantafyllou, Charalampos Agakidis, Olga Maliachova, Athanasios Christoforidis
P2-P381
Autoimmune thyroiditis in Klippel-Feil syndrome with Arnold Chiari and syringomyelia
Elisa Guidoni, Federica Lotti, Ursula Geronzi, Laura Arianna Sorrentino, Giovanna Municchi
Autoimmune thyroiditis in Klippel-Feil syndrome with Arnold Chiari and syringomyelia
Elisa Guidoni, Federica Lotti, Ursula Geronzi, Laura Arianna Sorrentino, Giovanna Municchi
P2-P382
Neonatal monitoring of newborns born from mothers with Graves' disease. Results of a retrospective monocentric study
Cécile Dumaine, Sophie Guilmin Crépon, Justine Pages, Didier Chevenne, Jonathan Rosenblatt, Caroline Storey, Laetitia Martinerie, Jean-Claude Carel, Delphine Zenaty, Juliane Léger, Dominique Simon
Neonatal monitoring of newborns born from mothers with Graves' disease. Results of a retrospective monocentric study
Cécile Dumaine, Sophie Guilmin Crépon, Justine Pages, Didier Chevenne, Jonathan Rosenblatt, Caroline Storey, Laetitia Martinerie, Jean-Claude Carel, Delphine Zenaty, Juliane Léger, Dominique Simon
P2-P383
A successful switch experience from high-dose PTU to MMI on day 4 of Graves’ thyroid storm in a 14-year-old girl
Hiroyuki Shinohara, Atsushi Iwabuchi, Akiko Yamada, Tomomi Kai, Tomohiro Kamoda
A successful switch experience from high-dose PTU to MMI on day 4 of Graves’ thyroid storm in a 14-year-old girl
Hiroyuki Shinohara, Atsushi Iwabuchi, Akiko Yamada, Tomomi Kai, Tomohiro Kamoda
P2-P384
Graves’s disease during pregnancy: the impact on the fetus and the newborn
Florine Belin, Danielle Rodrigue, Claire Claire Bouvattier, Cécile Teinturier, Khadidja Fouati, Agnès Linglart, Anne-Sophie Lambert
Graves’s disease during pregnancy: the impact on the fetus and the newborn
Florine Belin, Danielle Rodrigue, Claire Claire Bouvattier, Cécile Teinturier, Khadidja Fouati, Agnès Linglart, Anne-Sophie Lambert
P2-P385
Thyroid Hormone Receptor β (THRB) mutation: two new cases of heterozygous mutation with significant family history
James Blackburn, Senthil Senniappan, Dinesh Giri
Thyroid Hormone Receptor β (THRB) mutation: two new cases of heterozygous mutation with significant family history
James Blackburn, Senthil Senniappan, Dinesh Giri
P2-P386
Triac treatment response to thyroid hormone resistantance
Peyami Cinaz, Aylin Kılınç Uğurlu, Esra Döğer, Emine Demet Akbaş, Aysun Bideci, Orhun Çamurdan
Triac treatment response to thyroid hormone resistantance
Peyami Cinaz, Aylin Kılınç Uğurlu, Esra Döğer, Emine Demet Akbaş, Aysun Bideci, Orhun Çamurdan
P2-P387
Phenotype and genotype of four patients with thyroid hormone resistance syndrome due to mutations in the THRB gene
Meropi Toumba, Vassos Neocleous, Pavlos Fanis, Nicos Skordis, Leonidas A Phylactou, George A Tanteles, Marinella Kyriakidou-Himonas, Michalis Picolos
Phenotype and genotype of four patients with thyroid hormone resistance syndrome due to mutations in the THRB gene
Meropi Toumba, Vassos Neocleous, Pavlos Fanis, Nicos Skordis, Leonidas A Phylactou, George A Tanteles, Marinella Kyriakidou-Himonas, Michalis Picolos
P2-P388
Clinical course in a girl with two hTPO mutations - homozygous c.1268G>A (p.Gly393Arg) and heterozygous c.208C>G (p.Ala70Pro): 27 years of follow up
Iva Stoeva, Kalina Mihova, Reni Koleva, Mitko Zheliaskov, Boris Stoilov, Radka Kaneva
Clinical course in a girl with two hTPO mutations - homozygous c.1268G>A (p.Gly393Arg) and heterozygous c.208C>G (p.Ala70Pro): 27 years of follow up
Iva Stoeva, Kalina Mihova, Reni Koleva, Mitko Zheliaskov, Boris Stoilov, Radka Kaneva
P2-P389
A neurological disease mimicking central hypothyroidism: MCT8 deficiency
Ozgecan Demirbas, Erdal Eren, Omer Tarim
A neurological disease mimicking central hypothyroidism: MCT8 deficiency
Ozgecan Demirbas, Erdal Eren, Omer Tarim
P2-P390
Multinodular goiter in childhood: look for DICER1 mutation
Valentine SUTEAU, SOUTO Isabelle, BOUHOURS-NOUET Natacha, AZGAL Maryam, BAILLEUL Justine, CAMPAS Marie-Neige, DONZEAU Aurélie, RODIEN Patrice, COUTANT Régis
Multinodular goiter in childhood: look for DICER1 mutation
Valentine SUTEAU, SOUTO Isabelle, BOUHOURS-NOUET Natacha, AZGAL Maryam, BAILLEUL Justine, CAMPAS Marie-Neige, DONZEAU Aurélie, RODIEN Patrice, COUTANT Régis
P2-P391
Application of elastography in assesment of different benign thyroid lesions in children and adolescents
Hanna Borysewicz-Sańczyk, Janusz Dzięcioł, Beata Sawicka, Patrycja Florczykowska, Małgorzata Przychodzen, Artur Bossowski
Application of elastography in assesment of different benign thyroid lesions in children and adolescents
Hanna Borysewicz-Sańczyk, Janusz Dzięcioł, Beata Sawicka, Patrycja Florczykowska, Małgorzata Przychodzen, Artur Bossowski
P2-P392
Clinical characteristics and predictive factors for the detection of thyroid cancer in children with thyroid nodules
Junghwan Suh, Han Saem Choi, Ah Reum Kwon, Hyun Wook Chae, Duk Hee Kim, Ho-Seong Kim
Clinical characteristics and predictive factors for the detection of thyroid cancer in children with thyroid nodules
Junghwan Suh, Han Saem Choi, Ah Reum Kwon, Hyun Wook Chae, Duk Hee Kim, Ho-Seong Kim
P2-P393
Thyroid nodules in Prader-Willi syndrome
Graziano Grugni, Alessandro Minocci, Alessandro Sartorio, Antonino Crinò
Thyroid nodules in Prader-Willi syndrome
Graziano Grugni, Alessandro Minocci, Alessandro Sartorio, Antonino Crinò
P2-P394
Early Medullary Thyroid Carcinoma (MTC) in an infant with multiple endocrine neoplasia Type 2B (MEN2B, RETS Mutation codon 891)
Fawziya Alkhalaf, Ashraf Soliman
Early Medullary Thyroid Carcinoma (MTC) in an infant with multiple endocrine neoplasia Type 2B (MEN2B, RETS Mutation codon 891)
Fawziya Alkhalaf, Ashraf Soliman
P2-P395
Serum level of biotin rather than the daily dose is the main determinant of the interference on thyroid function assays in patients with biotinidase deficiency
ahu paketçi, engin köse, özlem gürsoy çalan, sezer acar, pelin teke, ferhat demirci, ayhan abacı, korcan demir, nur arslan, ece böber
Serum level of biotin rather than the daily dose is the main determinant of the interference on thyroid function assays in patients with biotinidase deficiency
ahu paketçi, engin köse, özlem gürsoy çalan, sezer acar, pelin teke, ferhat demirci, ayhan abacı, korcan demir, nur arslan, ece böber
P2-P396
Thyroid function tests and affecting factors in twins and triplets
Emre Kelesoglu, Zeynep Atay, Saygin Abali, Enver Atay, Murat Turan, Semra Gundogdu, Omer Ceran
Thyroid function tests and affecting factors in twins and triplets
Emre Kelesoglu, Zeynep Atay, Saygin Abali, Enver Atay, Murat Turan, Semra Gundogdu, Omer Ceran
P2-P397
Hypothyroidism in a child during treatment with nivolumab for a glioblastoma
Niels H Birkebaek, Christine Dahl
Hypothyroidism in a child during treatment with nivolumab for a glioblastoma
Niels H Birkebaek, Christine Dahl
P2-P398
Diagnosis and clinical course of amiodarone induced hyperthyroidism in three adolescent patients
Julia Gesing, Julia Hoppmann, Roman Gebauer, Roland Pfäffle, Astrid Bertsche, Wieland Kiess
Diagnosis and clinical course of amiodarone induced hyperthyroidism in three adolescent patients
Julia Gesing, Julia Hoppmann, Roman Gebauer, Roland Pfäffle, Astrid Bertsche, Wieland Kiess
P2-P399
Allogenic bone marrow transplantation in children: effect on thyroid function
Elpis Athina Vlachopapadopoulou, Anna Paisiou, Stefanos Stergiotis, Eleni Dikaia Ioannidou, Eugenios Goussetis, Maria Kafetzi, Vassiliki Kitra, Stefanos Michalacos
Allogenic bone marrow transplantation in children: effect on thyroid function
Elpis Athina Vlachopapadopoulou, Anna Paisiou, Stefanos Stergiotis, Eleni Dikaia Ioannidou, Eugenios Goussetis, Maria Kafetzi, Vassiliki Kitra, Stefanos Michalacos
P2-P400
Follow-up in children with non-obese and non-autoimmune subclinical hypothyroidism
Zeynep Ergin, Senay Savas-Erdeve, Erdal Kurnaz, Semra Cetinkaya, Zehra Aycan
Follow-up in children with non-obese and non-autoimmune subclinical hypothyroidism
Zeynep Ergin, Senay Savas-Erdeve, Erdal Kurnaz, Semra Cetinkaya, Zehra Aycan
P2-P401
Clinical management of childhood hyperthyroidism:a longitudinal study at a single center
Tiago Jeronimo Dos Santos, Gabriel Martos-Moreno, María Muñoz-Calvo, Jesús Pozo, Fernando Rodríguez-Artalejo, Jesús Argente
Clinical management of childhood hyperthyroidism:a longitudinal study at a single center
Tiago Jeronimo Dos Santos, Gabriel Martos-Moreno, María Muñoz-Calvo, Jesús Pozo, Fernando Rodríguez-Artalejo, Jesús Argente
P2-P402
Association of thyroid stimulating hormone and free thyroxine with cardiometabolic risk factors in Euthyroid Korean children and adolescents aged 10-18 years: the Korean National Health and Nutrition Examination Survey 2015
Jung Sub Lim, Young Suk Shim, Eun Young Kim
Association of thyroid stimulating hormone and free thyroxine with cardiometabolic risk factors in Euthyroid Korean children and adolescents aged 10-18 years: the Korean National Health and Nutrition Examination Survey 2015
Jung Sub Lim, Young Suk Shim, Eun Young Kim
P2-P403
Asymptomatic hyperthyrotropinaemia in children, does it correlate to true thyroid gland dysfunction?
Kalliopi Kappou, Vasiliki Bisbinas, Zacharoula Karabouta
Asymptomatic hyperthyrotropinaemia in children, does it correlate to true thyroid gland dysfunction?
Kalliopi Kappou, Vasiliki Bisbinas, Zacharoula Karabouta
P2-P404
Hearing loss among patients with Congenital Hypothyroidism
Tal Almagor, Dan Nachtigal, Zohara Sharoni, Ghadir Elias-Assad, Ora Hess, Gilad Havazelet, Yardena Tenenbaum-Rakover
Hearing loss among patients with Congenital Hypothyroidism
Tal Almagor, Dan Nachtigal, Zohara Sharoni, Ghadir Elias-Assad, Ora Hess, Gilad Havazelet, Yardena Tenenbaum-Rakover
P2-P406
Absence of uptake on scintigraphy does not always correlate with athyreosis: Re-evaluation of patients diagnosed with athyreosis over a 10 year period in the Republic of Ireland
N McGrath, CP Hawkes, S Ryan, P Mayne, NP Murphy
Absence of uptake on scintigraphy does not always correlate with athyreosis: Re-evaluation of patients diagnosed with athyreosis over a 10 year period in the Republic of Ireland
N McGrath, CP Hawkes, S Ryan, P Mayne, NP Murphy
P2-P407
Bannayan-Riley-Ruvalcaba syndrome with PTEN mutation in a patient affected by Congenital Hypothyroidism due to TPO gene alteration
Gaia Vincenzi, Maria Cristina Vigone, Elena Peroni, Luca Saracco, Pier Luigi Paesano, Riccardo Maggiore, Gilberto Mari, Maria Grazia Patricelli, Giovanna Weber
Bannayan-Riley-Ruvalcaba syndrome with PTEN mutation in a patient affected by Congenital Hypothyroidism due to TPO gene alteration
Gaia Vincenzi, Maria Cristina Vigone, Elena Peroni, Luca Saracco, Pier Luigi Paesano, Riccardo Maggiore, Gilberto Mari, Maria Grazia Patricelli, Giovanna Weber
P2-P408
THE CONGENITAL HYPOTHYROIDISM SCREENING PROGRAMME IN A SIGLE ITALIAN CENTRE: A 5-YEARS RETROSPECTIVE STUDY
Maria Cristina Maggio, Saveria Sabrina Ragusa, Tommaso Silvano Aronica, Orazia Maria Granata, Eleonora Gucciardino, Giovanni Corsello
THE CONGENITAL HYPOTHYROIDISM SCREENING PROGRAMME IN A SIGLE ITALIAN CENTRE: A 5-YEARS RETROSPECTIVE STUDY
Maria Cristina Maggio, Saveria Sabrina Ragusa, Tommaso Silvano Aronica, Orazia Maria Granata, Eleonora Gucciardino, Giovanni Corsello
P2-P409
Do insulin like growth factors also influence growth in children with congenital hypothyroidism:a cohort analysis
Sangita Yadav, Ruchi Goel, Mukta Mantan, T K Mishra
Do insulin like growth factors also influence growth in children with congenital hypothyroidism:a cohort analysis
Sangita Yadav, Ruchi Goel, Mukta Mantan, T K Mishra
P2-P410
Study of hearing function in children with Congenital Hypothyroidism attending Alexandria University Children's Hospital
Shaymaa Elsayed, Ehsan Wafa, Doaa Elmoazen, Haidy Elsayed
Study of hearing function in children with Congenital Hypothyroidism attending Alexandria University Children's Hospital
Shaymaa Elsayed, Ehsan Wafa, Doaa Elmoazen, Haidy Elsayed
P2-P411
Awareness of the risks of acquired iodine deficiency in strict Vegan diets
Agnieszka Brandt, Moira Cheung, Sophia Sakka, Michal Ajzensztejn, Tony Hulse
Awareness of the risks of acquired iodine deficiency in strict Vegan diets
Agnieszka Brandt, Moira Cheung, Sophia Sakka, Michal Ajzensztejn, Tony Hulse
P2-P412
Thyroid function in the Korean obese children and adolescents: Korea National Health and Nutrition Examination Survey 2013 to 2015
Youngmin An, Ji Eun Lee, Young Ju Suh
Thyroid function in the Korean obese children and adolescents: Korea National Health and Nutrition Examination Survey 2013 to 2015
Youngmin An, Ji Eun Lee, Young Ju Suh
P3-P361
Prevalence and demographic profile of thyroid disorders in Indian children
aashish sethi, Smita Ramachandran, Inderpal Kochar
Prevalence and demographic profile of thyroid disorders in Indian children
aashish sethi, Smita Ramachandran, Inderpal Kochar
P3-P362
Graves’ Disease in a Pediatric Population: results from the last 17 years at a Pediatric Endocrinology Unit
Fábia Carvalho, Sílvia Paredes, Maria Miguel Gomes, Sofia Martins, Olinda Marques, Ana Antunes
Graves’ Disease in a Pediatric Population: results from the last 17 years at a Pediatric Endocrinology Unit
Fábia Carvalho, Sílvia Paredes, Maria Miguel Gomes, Sofia Martins, Olinda Marques, Ana Antunes
P3-P363
Acquired severe hypothyroidism in children – forgotten or unbelievable diagnosis in a time of large and easy availability of thyroid tests?
Anna Kucharska, Dominika Labochka, Ada Borowiec, Ewelina Witkowska- Sedek, Beata Pyrzak
Acquired severe hypothyroidism in children – forgotten or unbelievable diagnosis in a time of large and easy availability of thyroid tests?
Anna Kucharska, Dominika Labochka, Ada Borowiec, Ewelina Witkowska- Sedek, Beata Pyrzak
P3-P364
Thyroid disorders and autoimmunity in children and adolescents with Type 1 (T1DM) and Type 2 Diabetes Mellitus (T2DM)
ASHRAF Soliman, Fawzia Alyafei, fawziya Alkhalaf, Amal Sabt, Reem waseef, Nagwa Aldarsy
Thyroid disorders and autoimmunity in children and adolescents with Type 1 (T1DM) and Type 2 Diabetes Mellitus (T2DM)
ASHRAF Soliman, Fawzia Alyafei, fawziya Alkhalaf, Amal Sabt, Reem waseef, Nagwa Aldarsy
P3-P365
The reference and follow-up signs and symptoms of the cases who are diagnosed as Hyperthyroidism
Elif Gokce Demir, Ayla Guven, Metin Yildiz
The reference and follow-up signs and symptoms of the cases who are diagnosed as Hyperthyroidism
Elif Gokce Demir, Ayla Guven, Metin Yildiz
P3-P366
Clinical features in childhood Graves' Disease
Aylin Kılınç Uğurlu, Esra Döğer, Emine Demet Akbaş, Aysun Bideci, Orhun Çamurdan, Peyami Cinaz
Clinical features in childhood Graves' Disease
Aylin Kılınç Uğurlu, Esra Döğer, Emine Demet Akbaş, Aysun Bideci, Orhun Çamurdan, Peyami Cinaz
P3-P367
General characteristics of Autoimmune Thyroid Diseases and evaluation of accompanied Morbiditis
Aysel Burcu Palandökenlier İbili, Beray Selver Eklioğlu, Mehmet Emre Atabek
General characteristics of Autoimmune Thyroid Diseases and evaluation of accompanied Morbiditis
Aysel Burcu Palandökenlier İbili, Beray Selver Eklioğlu, Mehmet Emre Atabek
P3-P368
Amiodarone induced hyperthyroidism in a pediatric patient
Bernardo Marques, Sofia Oliveira, Sérgio Laranjo, Lurdes Lopes
Amiodarone induced hyperthyroidism in a pediatric patient
Bernardo Marques, Sofia Oliveira, Sérgio Laranjo, Lurdes Lopes
P3-P369
Inefficiency of levothyroxine suspension in a neonate with congenital hypothyroidism
Carla Z. Minutti, Jacqueline Chan, Fabiola D'Ambrosio
Inefficiency of levothyroxine suspension in a neonate with congenital hypothyroidism
Carla Z. Minutti, Jacqueline Chan, Fabiola D'Ambrosio
P3-P370
Thyroid carcinoma in children: 7 years’ experience of a single center
Cristina Preda, Gabriela Delia Ciobanu, Maria-Christina Ungureanu, Letitia Elena Leustean, Laura Teodoriu, Raluca Balaceanu, Alexandru Grigorovici
Thyroid carcinoma in children: 7 years’ experience of a single center
Cristina Preda, Gabriela Delia Ciobanu, Maria-Christina Ungureanu, Letitia Elena Leustean, Laura Teodoriu, Raluca Balaceanu, Alexandru Grigorovici
P3-P371
Autoimmune thyroiditis (Hashimoto thyroiditis) in a known case of autoimmune hemolytic anemia
Dina fawzy, Nesreen Eliwa
Autoimmune thyroiditis (Hashimoto thyroiditis) in a known case of autoimmune hemolytic anemia
Dina fawzy, Nesreen Eliwa
P3-P372
Dento - maxillary and periodontal changes in puberty / adolescence in subclinical hypothyroidism of autoimmune cause
Eduard Circo, Cristina Gosu, Seila Ibadula, Razvan Circo
Dento - maxillary and periodontal changes in puberty / adolescence in subclinical hypothyroidism of autoimmune cause
Eduard Circo, Cristina Gosu, Seila Ibadula, Razvan Circo
P3-P373
Hypovitaminosis D and chronic autoimmune thyroiditis mammary echostructural involvements in puberty
Seila Ibadula, Eduard Circo
Hypovitaminosis D and chronic autoimmune thyroiditis mammary echostructural involvements in puberty
Seila Ibadula, Eduard Circo
P3-P374
Two contrasting cases of solitary thyroid nodules in adolescent girls
Eleanor Walder, Vijith Puthi
Two contrasting cases of solitary thyroid nodules in adolescent girls
Eleanor Walder, Vijith Puthi
P3-P375
Congenital Hypothyroidism - diagnose early and keep going
Elena Sergeyev, Anette Sloltze, Wieland Kiess, Roland Pfaeffle, Antje Koerner
Congenital Hypothyroidism - diagnose early and keep going
Elena Sergeyev, Anette Sloltze, Wieland Kiess, Roland Pfaeffle, Antje Koerner
P3-P376
An impressive recovery of arrested growth and puberty in a 13 year old boy after being treated for simultaneously diagnosed severe hypothyroidism and coeliac disease
Olga Fafoula, Eleni Panagouli, Argyro Panagiotakou, Maria Mpeni, Chrisitina Georgila, Paraskevi Korovessi, Stauroula Kostaridou
An impressive recovery of arrested growth and puberty in a 13 year old boy after being treated for simultaneously diagnosed severe hypothyroidism and coeliac disease
Olga Fafoula, Eleni Panagouli, Argyro Panagiotakou, Maria Mpeni, Chrisitina Georgila, Paraskevi Korovessi, Stauroula Kostaridou
P3-P377
A very rare thyroid hormone resistance case having heterozygous mutation in THRB genes
mehmet keskin, seniha kiremitçi yılmaz, emel hatun aytaç kaplan, murat karaoğlan, kadri karaer, özlem keskin
A very rare thyroid hormone resistance case having heterozygous mutation in THRB genes
mehmet keskin, seniha kiremitçi yılmaz, emel hatun aytaç kaplan, murat karaoğlan, kadri karaer, özlem keskin
P3-P378
Clinical Case (children's endocrinology)
Ieva Strauhmane, Gunda Zvigule - Neidere, Ieva Kravale, Iveta dzivite-Krisane, inita kaze
Clinical Case (children's endocrinology)
Ieva Strauhmane, Gunda Zvigule - Neidere, Ieva Kravale, Iveta dzivite-Krisane, inita kaze
P3-P379
Thyroid imaging study for the diagnosis of Congenital Hypothyroidism with Thyroid Dysgenesis
Sangwoo Chun, Jeesuk Yu
Thyroid imaging study for the diagnosis of Congenital Hypothyroidism with Thyroid Dysgenesis
Sangwoo Chun, Jeesuk Yu
P3-P380
A case of permanent congenital hypothyroidism with compound heterozygous mutations in the DUOX2 gene
Jeongju Hwang, Ja-Hyun Jang, Jeesuk Yu
A case of permanent congenital hypothyroidism with compound heterozygous mutations in the DUOX2 gene
Jeongju Hwang, Ja-Hyun Jang, Jeesuk Yu
P3-P381
Growth catch-up on acquired hypothyroidism presenting with growth delay
Joana Serra-Caetano, Patrícia Miranda, Ana Ferraz, Ana Lopes Dias, Adriana Lages, Rita Cardoso, Isabel Dinis, Alice Mirante
Growth catch-up on acquired hypothyroidism presenting with growth delay
Joana Serra-Caetano, Patrícia Miranda, Ana Ferraz, Ana Lopes Dias, Adriana Lages, Rita Cardoso, Isabel Dinis, Alice Mirante
P3-P382
Thyroid disease in children and adolescences with Down Syndrome– 16 years of follow up in a single service
Maria Claudia Schmitt-Lobe, Hamilton Fogaça, Aline Scheidemantel, Mariel Correa Nepomuceno
Thyroid disease in children and adolescences with Down Syndrome– 16 years of follow up in a single service
Maria Claudia Schmitt-Lobe, Hamilton Fogaça, Aline Scheidemantel, Mariel Correa Nepomuceno
P3-P383
Corticosteroid resistant Immune Thrombocytopenic Purpura, is it a marker of future Graves Disease?
Maria Cristina Azcona, Jose Luis Leon, Monica Prados, Amaia Ochotorena, Asier Oliver
Corticosteroid resistant Immune Thrombocytopenic Purpura, is it a marker of future Graves Disease?
Maria Cristina Azcona, Jose Luis Leon, Monica Prados, Amaia Ochotorena, Asier Oliver
P3-P384
Neonatal hypothyroidism following transplacental amiodarone treatment for supraventricular tachyarrhythmia
Maria Korpal-Szczyrska, Malgorzata Mysliwiec, Jozef Szczyrski
Neonatal hypothyroidism following transplacental amiodarone treatment for supraventricular tachyarrhythmia
Maria Korpal-Szczyrska, Malgorzata Mysliwiec, Jozef Szczyrski
P3-P385
Rare case report of thyroiditis De Quervain in a six years old girl
Maria Liapi, Norbert Jorch, Eckard Hamelmann
Rare case report of thyroiditis De Quervain in a six years old girl
Maria Liapi, Norbert Jorch, Eckard Hamelmann
P3-P386
Papillary thyroid carcinoma in a 7 year old boy presenting with a goiter without microcalcifications and enlarged cervical lymph nodes
Marianne Becker, Letizia Vega, Carine De Beaufort, Paul Philippe, Isabelle Kieffer
Papillary thyroid carcinoma in a 7 year old boy presenting with a goiter without microcalcifications and enlarged cervical lymph nodes
Marianne Becker, Letizia Vega, Carine De Beaufort, Paul Philippe, Isabelle Kieffer
P3-P387
Graves' disease, Methimazole and SLE-like reaction:a case report
Michael Yafi, Chanthu Pillai, Charles Cox
Graves' disease, Methimazole and SLE-like reaction:a case report
Michael Yafi, Chanthu Pillai, Charles Cox
P3-P388
A rare case of pediatric hyperthyroidism
Sara Ciccone, Graziamaria Ubertini, Manuela Pasini, Marcello Stella
A rare case of pediatric hyperthyroidism
Sara Ciccone, Graziamaria Ubertini, Manuela Pasini, Marcello Stella
P3-P389
Allan–Herndon–Dudley syndrome in a patient with Global delay development – a case report
Shahab Noorian,
Allan–Herndon–Dudley syndrome in a patient with Global delay development – a case report
Shahab Noorian,
P3-P390
Multi autoimmune phenomenon in Indian children with thyroid disorder
Smita Ramachandran, Aashish Sethi, Inderpal Kochar
Multi autoimmune phenomenon in Indian children with thyroid disorder
Smita Ramachandran, Aashish Sethi, Inderpal Kochar
P3-P391
Levothyroxine treatment of Subclinical (SH) and Overt (OH) Hypothyroidism in children with Autoimmune Hashimoto Thyroiditis (AHT): a retrospective study in regard with TSH and Free T4 (FT4) at diagnosis
Sofia LEKA-EMIRI, Vassilios PETROU, Cathrine EVANGELOPOULOU, Maria KAFETZI, Aspasia FOTINOU, Elpis VLACHOPAPADOPOULOU, Stefanos MICHALACOS
Levothyroxine treatment of Subclinical (SH) and Overt (OH) Hypothyroidism in children with Autoimmune Hashimoto Thyroiditis (AHT): a retrospective study in regard with TSH and Free T4 (FT4) at diagnosis
Sofia LEKA-EMIRI, Vassilios PETROU, Cathrine EVANGELOPOULOU, Maria KAFETZI, Aspasia FOTINOU, Elpis VLACHOPAPADOPOULOU, Stefanos MICHALACOS
P3-P392
Hashitoxicosis:a rare diagnosis in childhood
Elpis Athina Vlachopapadopoulou, Stefanos Stergiotis, Eirini Dikaiakou, Maria Kafetzi, Marina Vakaki, Aspasia Fotinou, Stefanos Michalacos
Hashitoxicosis:a rare diagnosis in childhood
Elpis Athina Vlachopapadopoulou, Stefanos Stergiotis, Eirini Dikaiakou, Maria Kafetzi, Marina Vakaki, Aspasia Fotinou, Stefanos Michalacos
P3-P393
An assay led astray: a curious case of biotin-induced hyperthyroidism
Tashunka Taylor-Miller, Ashely Alexander, Tina Yen, Michele O'Connell
An assay led astray: a curious case of biotin-induced hyperthyroidism
Tashunka Taylor-Miller, Ashely Alexander, Tina Yen, Michele O'Connell
P3-P394
A case of steroid-responsive encephalopathy associated with autoimmune thyroiditis (SREAT) in a girl with newly diagnosed Hashimoto thyroiditis
Yijuan Yvonne Lim, Anjian Andrew Sng, Cindy Wei-li Ho, Yung-Seng Lee, Kah-Yin Loke
A case of steroid-responsive encephalopathy associated with autoimmune thyroiditis (SREAT) in a girl with newly diagnosed Hashimoto thyroiditis
Yijuan Yvonne Lim, Anjian Andrew Sng, Cindy Wei-li Ho, Yung-Seng Lee, Kah-Yin Loke
P3-P395
Intellectual outcome at childhood in congenital hypothyroidism according to etiology and treatment related factors
Yong Hee Hong
Intellectual outcome at childhood in congenital hypothyroidism according to etiology and treatment related factors
Yong Hee Hong
P3-P396
Myastenia gravis in a girl with Hashimoto thyroiditis
Zoran Gucev, Laerta Alili, Nevenka Laban, Velibor Tasic
Myastenia gravis in a girl with Hashimoto thyroiditis
Zoran Gucev, Laerta Alili, Nevenka Laban, Velibor Tasic
P3-P397
Head circumference, birth length, and weight of neonates of mothers with hypothyroidism
Tamar Laron-Kenet, Aviva Silbergeld, Pearl Lilos, Zvi Laron
Head circumference, birth length, and weight of neonates of mothers with hypothyroidism
Tamar Laron-Kenet, Aviva Silbergeld, Pearl Lilos, Zvi Laron
RFC5.1
Serum levels of the soluble receptor for advanced glycation end products are reduced in children with Hashimoto’s Thyroiditis
Tommaso Aversa, Rosaria Maddalena Ruggeri, Domenico Corica, Maria Teresa Cristani, Silvestro Mirabelli, Teresa Maria Vicchio, Francesco Trimarchi, Filippo De Luca, Malgorzata Wasniewska
Serum levels of the soluble receptor for advanced glycation end products are reduced in children with Hashimoto’s Thyroiditis
Tommaso Aversa, Rosaria Maddalena Ruggeri, Domenico Corica, Maria Teresa Cristani, Silvestro Mirabelli, Teresa Maria Vicchio, Francesco Trimarchi, Filippo De Luca, Malgorzata Wasniewska
RFC5.2
Analysis of chosen polymorphisms rs7138803 A/G - FAIM2, rs7093069 C/T - IL-2RA, rs5742909 C/T - CTLA-4 in pathogenesis of Hashimoto's thyroiditis in children
Artur Bossowski, Joanna Gościk, Natalia Wawrusiewicz-Kurylonek, Anna Bossowska, Tommaso Aversa, Domenico Corica, Adam Krętowski, Małgorzata Waśniewska
Analysis of chosen polymorphisms rs7138803 A/G - FAIM2, rs7093069 C/T - IL-2RA, rs5742909 C/T - CTLA-4 in pathogenesis of Hashimoto's thyroiditis in children
Artur Bossowski, Joanna Gościk, Natalia Wawrusiewicz-Kurylonek, Anna Bossowska, Tommaso Aversa, Domenico Corica, Adam Krętowski, Małgorzata Waśniewska
RFC5.3
Incidence and treatment outcome of childhood thyrotoxicosis
Maria Rodanaki, Maria Lodefalk, Jan Åman
Incidence and treatment outcome of childhood thyrotoxicosis
Maria Rodanaki, Maria Lodefalk, Jan Åman
RFC5.4
The value of cytological, histological and US examination to determine of management children with nodular goiter
Dmitriy Brovin, Valentina Peterkova, Alexander Anikiev, Oleg Danilenko, Nikolay Kuznetsov
The value of cytological, histological and US examination to determine of management children with nodular goiter
Dmitriy Brovin, Valentina Peterkova, Alexander Anikiev, Oleg Danilenko, Nikolay Kuznetsov
RFC5.5
Evidence for a founder effect in Multiple Endocrine Neoplasia 2
Pavlos Fanis, Nicos Skordis, Savvas Frangos, George Christopoulos, Elena Spanou-Aristidou, Elena Andreou, Panayiotis Manoli, Michalis Mavrommatis, Stella Nicolaou, Marina Kleanthous, Marios A Cariolou, Violetta Christophidou-Anastasiadou, George A Tanteles, Leonidas A Phylactou, Vassos Neocleous
Evidence for a founder effect in Multiple Endocrine Neoplasia 2
Pavlos Fanis, Nicos Skordis, Savvas Frangos, George Christopoulos, Elena Spanou-Aristidou, Elena Andreou, Panayiotis Manoli, Michalis Mavrommatis, Stella Nicolaou, Marina Kleanthous, Marios A Cariolou, Violetta Christophidou-Anastasiadou, George A Tanteles, Leonidas A Phylactou, Vassos Neocleous
RFC5.6
DUOX2 deficiency in Quebec: from life-threatening compressive goiter in infancy to lifelong euthyroidism
Gabrielle Dufort, Stéphanie Larrivée-Vanier, Dardye Eugène, Xavier De Deken, Karl Heinimann, Gabor Szinnai, Guy Van Vliet, Johnny Deladoëy
DUOX2 deficiency in Quebec: from life-threatening compressive goiter in infancy to lifelong euthyroidism
Gabrielle Dufort, Stéphanie Larrivée-Vanier, Dardye Eugène, Xavier De Deken, Karl Heinimann, Gabor Szinnai, Guy Van Vliet, Johnny Deladoëy
FC6.1
Correlations between measures of adiposity across childhood and adolescence and the intestinal microbiota in 15-17 year-old children with a family history of obesity: preliminary findings from the QUALITY cohort
Mélanie Henderson, Andraea Van Hulst, Gabrielle Simoneau, Tracie A. Barnett, Vicky Drapeau, Marie-Ève Mathieu, Belinda Nicolau, Thibaut Varin, André Marette
Correlations between measures of adiposity across childhood and adolescence and the intestinal microbiota in 15-17 year-old children with a family history of obesity: preliminary findings from the QUALITY cohort
Mélanie Henderson, Andraea Van Hulst, Gabrielle Simoneau, Tracie A. Barnett, Vicky Drapeau, Marie-Ève Mathieu, Belinda Nicolau, Thibaut Varin, André Marette
FC6.2
Impaired Brain Satiety Responses to a Meal in Children with Obesity
Christian Roth, Susan Melhorn, Clinton Elfers, Kelley Scholz, Mary Rosalynn De Leon, Brian Saelens, Ellen Schur
Impaired Brain Satiety Responses to a Meal in Children with Obesity
Christian Roth, Susan Melhorn, Clinton Elfers, Kelley Scholz, Mary Rosalynn De Leon, Brian Saelens, Ellen Schur
FC6.3
Role of PTEN in the proliferation and differentiation of preadipocytes
Anna Kirstein, Franziska Kässner, Gordian L. Schmid, Norman Händel, Melanie Penke, Wieland Kiess, Antje Garten
Role of PTEN in the proliferation and differentiation of preadipocytes
Anna Kirstein, Franziska Kässner, Gordian L. Schmid, Norman Händel, Melanie Penke, Wieland Kiess, Antje Garten
FC6.4
Identification of the first obesity-associated mutations in human mesoderm-specific transcript (MEST) result in protein overexpression, adipocyte hypertrophy and a reduction in adipocyte mitochondrial area
Juan Suárez, Gabriel Martos-Moreno, Patricia Rivera, Clara Serra-Juhé, Julie Chowen, Luis Pérez-Jurado, Jesús Argente
Identification of the first obesity-associated mutations in human mesoderm-specific transcript (MEST) result in protein overexpression, adipocyte hypertrophy and a reduction in adipocyte mitochondrial area
Juan Suárez, Gabriel Martos-Moreno, Patricia Rivera, Clara Serra-Juhé, Julie Chowen, Luis Pérez-Jurado, Jesús Argente
FC6.5
The role of adipocytes in childhood precursor Bcell lymphoblastic leukemia
Elena Dorothea Brenner, Julia Zinngrebe, Meike Dahlhaus, Lueder-Hinrich Meyer, Martin Wabitsch, Klaus-Michael Debatin, Pamela Fischer-Posovszky
The role of adipocytes in childhood precursor Bcell lymphoblastic leukemia
Elena Dorothea Brenner, Julia Zinngrebe, Meike Dahlhaus, Lueder-Hinrich Meyer, Martin Wabitsch, Klaus-Michael Debatin, Pamela Fischer-Posovszky
FC6.6
MicroRNA-141 directly targets and inhibits sirtuins 1 gene expression and its elevation in obese subjects is responsible for reduced levels of sirtuin1 and the subsequent hepatic steatosis and insulin resistance
Mitra Nourbakhsh, Zeynab Yousefi, Nikta Dadkhah Nikroo, Mojtaba Malek, Abdolreza Pazouki, Somayye Mokhber
MicroRNA-141 directly targets and inhibits sirtuins 1 gene expression and its elevation in obese subjects is responsible for reduced levels of sirtuin1 and the subsequent hepatic steatosis and insulin resistance
Mitra Nourbakhsh, Zeynab Yousefi, Nikta Dadkhah Nikroo, Mojtaba Malek, Abdolreza Pazouki, Somayye Mokhber
LB-P11
Metabolic profile in survivors of pediatric hematopoietic stem cells transplantation after chemotherapy-only conditioning
Luminita-Nicoleta Cima, Lavinia Nedelea, Cristina Zaharia, Anca Colita, Carmen Gabriela Barbu, Simona Fica
Metabolic profile in survivors of pediatric hematopoietic stem cells transplantation after chemotherapy-only conditioning
Luminita-Nicoleta Cima, Lavinia Nedelea, Cristina Zaharia, Anca Colita, Carmen Gabriela Barbu, Simona Fica
P1-P093
Functional characterization of novel and known genetic variants in the leptin receptor (LEPR) gene of two patients with morbid obesity
Franziska Voigtmann, Stein Robert, Kathrin Landgraf, Rami Abou Jamra, Wieland Kiess, Antje Körner
Functional characterization of novel and known genetic variants in the leptin receptor (LEPR) gene of two patients with morbid obesity
Franziska Voigtmann, Stein Robert, Kathrin Landgraf, Rami Abou Jamra, Wieland Kiess, Antje Körner
P1-P094
Association of single nucleotide polymorphisms in TNFA, PNPLA3, ADIPOQ and APOC3 genes with obesity and non-alcoholic fatty liver disease in north Indian adolescents
Vandana Jain, Anil Kumar, Manisha Jana, Mani Kalaivani
Association of single nucleotide polymorphisms in TNFA, PNPLA3, ADIPOQ and APOC3 genes with obesity and non-alcoholic fatty liver disease in north Indian adolescents
Vandana Jain, Anil Kumar, Manisha Jana, Mani Kalaivani
P1-P095
Variation of Circulating Brain-Derived Neurotrophic Factor according to Gender, Body Mass Index and Metabolic Syndrome Parameters in Adolescents
Flora Bacopoulou, Christina Tsitsimpikou, Aimilia Mantzou, Despoina Apostolaki, Christina Darviri, Vasiliki Efthymiou
Variation of Circulating Brain-Derived Neurotrophic Factor according to Gender, Body Mass Index and Metabolic Syndrome Parameters in Adolescents
Flora Bacopoulou, Christina Tsitsimpikou, Aimilia Mantzou, Despoina Apostolaki, Christina Darviri, Vasiliki Efthymiou
P1-P096
Kisspeptin and the genetic obesidome
STYLIANI GERONIKOLOU, ATHANASSIA PAVLOPOULOU, KONSTANTINOS ALBANOPOULOS, DENNIS COKKINOS, CHRISTINA KANAKA-GANTENBEIN, GEORGE CHROUSOS
Kisspeptin and the genetic obesidome
STYLIANI GERONIKOLOU, ATHANASSIA PAVLOPOULOU, KONSTANTINOS ALBANOPOULOS, DENNIS COKKINOS, CHRISTINA KANAKA-GANTENBEIN, GEORGE CHROUSOS
P1-P097
Circulating exosomal miRNAs involved in the pathogenesis of children nonalcoholic steatohepatitis
xuelian Zhou, Junfen Fu, Guanping Dong, Ke Huang, Wei Wu
Circulating exosomal miRNAs involved in the pathogenesis of children nonalcoholic steatohepatitis
xuelian Zhou, Junfen Fu, Guanping Dong, Ke Huang, Wei Wu
P1-P098
Placental fatty acid profile, DNA methylation and adverse metabolic outcomes in the offspring at school age
Judit Bassols, Silvia Xargay-Torrent, Berta Mas-Pares, Esther Lizarraga-Mollinedo, Anna Prats-Puig, Alexandra Bonmatí, Jose-Maria Martinez-Calcerrada, Francis de Zegher, Lourdes Ibáñez, Abel Lopez-Bermejo
Placental fatty acid profile, DNA methylation and adverse metabolic outcomes in the offspring at school age
Judit Bassols, Silvia Xargay-Torrent, Berta Mas-Pares, Esther Lizarraga-Mollinedo, Anna Prats-Puig, Alexandra Bonmatí, Jose-Maria Martinez-Calcerrada, Francis de Zegher, Lourdes Ibáñez, Abel Lopez-Bermejo
P1-P099
Association of Serum Fibroblast Growth Factor 21 and Irisin with Insulin Sensitivity Markers and Serum Lipids in 12-year-old Children
Satu Seppä, Sirpa Tenhola, Raimo Voutilainen
Association of Serum Fibroblast Growth Factor 21 and Irisin with Insulin Sensitivity Markers and Serum Lipids in 12-year-old Children
Satu Seppä, Sirpa Tenhola, Raimo Voutilainen
P1-P100
Serum catestatin levels in obese children and adolescents
Marko Šimunović, Daniela Šupe-Domić, Željka Karin, Joško Božić, Ivana Unić, Veselin Škrabić
Serum catestatin levels in obese children and adolescents
Marko Šimunović, Daniela Šupe-Domić, Željka Karin, Joško Božić, Ivana Unić, Veselin Škrabić
P1-P101
Circulating MOTS-c levels are decreased in obese male children and adolescents and associated with insulin resistance.
Caiqi Du, Cai Zhang, Wei Wu, Yan Liang, Ling Hou, Anru Wang, Qin Ning, Xiaoping Luo
Circulating MOTS-c levels are decreased in obese male children and adolescents and associated with insulin resistance.
Caiqi Du, Cai Zhang, Wei Wu, Yan Liang, Ling Hou, Anru Wang, Qin Ning, Xiaoping Luo
P1-P102
Plasma adropin levels are associated with lipid characteristics amongst children with obesity
Ruimin Chen, Xin Yuan, Qian Ouyang, Zhuanzhuan Ai, Xiangquan Lin, Ying Zhang, Xiaohong Yang, Chunyan Cai
Plasma adropin levels are associated with lipid characteristics amongst children with obesity
Ruimin Chen, Xin Yuan, Qian Ouyang, Zhuanzhuan Ai, Xiangquan Lin, Ying Zhang, Xiaohong Yang, Chunyan Cai
P1-P103
Associations of non-high-density lipoprotein cholesterol with Metabolic Syndrome and its components in Korean children and adolescents: the Korea National Health and Nutrition Examination Surveys 2008-2014
Young Suk Shim, Hwal Rim Jeong, Seung Yang, Eun Young Kim, Il Tae Hwang
Associations of non-high-density lipoprotein cholesterol with Metabolic Syndrome and its components in Korean children and adolescents: the Korea National Health and Nutrition Examination Surveys 2008-2014
Young Suk Shim, Hwal Rim Jeong, Seung Yang, Eun Young Kim, Il Tae Hwang
P1-P104
Chromosomal deletions at chromosome 16p11.2 associated with severe early-onset obesity- 3 additional patients
Gloria Herrmann, Stefan Ehehalt, Guntram Borck, Martin Wabitsch, Julia von Schnurbein
Chromosomal deletions at chromosome 16p11.2 associated with severe early-onset obesity- 3 additional patients
Gloria Herrmann, Stefan Ehehalt, Guntram Borck, Martin Wabitsch, Julia von Schnurbein
P1-P105
Effect of a Melanocortin-4 Receptor (MC4R) Agonist, Setmelanotide, on obesity and hyperphagia in individuals affected by Alström syndrome
Joan C Han, Fred T Fiedorek, Michelle Hylan, Cathy Folster, Tarekegn Hiwot
Effect of a Melanocortin-4 Receptor (MC4R) Agonist, Setmelanotide, on obesity and hyperphagia in individuals affected by Alström syndrome
Joan C Han, Fred T Fiedorek, Michelle Hylan, Cathy Folster, Tarekegn Hiwot
P1-P106
Towards a greater understanding of the pathophysiology of obesity: hypothalamic obesity as a model of dysregulation of appetite and metabolic homeostasis
Hoong-Wei Gan, Clare Leeson, Helen Aitkenhead, Sadaf Farooqi, Helen Spoudeas, Mehul Dattani
Towards a greater understanding of the pathophysiology of obesity: hypothalamic obesity as a model of dysregulation of appetite and metabolic homeostasis
Hoong-Wei Gan, Clare Leeson, Helen Aitkenhead, Sadaf Farooqi, Helen Spoudeas, Mehul Dattani
P1-P107
Serum uric acid level and its association with metabolic syndrome in Korean adolescents
So Yoon Jung, Young Ah Lee, Jae Hyun Kim, Seong Yong Lee, Se Young Kim, Choong Ho Shin, Sei Won Yang
Serum uric acid level and its association with metabolic syndrome in Korean adolescents
So Yoon Jung, Young Ah Lee, Jae Hyun Kim, Seong Yong Lee, Se Young Kim, Choong Ho Shin, Sei Won Yang
P1-P108
More than a gut feeling: preliminary evidence supporting a role for lifestyle habits in shaping the intestinal microbiota in childhood and adolescence
Mélanie Henderson, Andraea Van Hulst, Gabrielle Simoneau, Tracie A. Barnett, Vicky Drapeau, Marie-Ève Mathieu, Belinda Nicolau, Thibaut Varin, André Marette
More than a gut feeling: preliminary evidence supporting a role for lifestyle habits in shaping the intestinal microbiota in childhood and adolescence
Mélanie Henderson, Andraea Van Hulst, Gabrielle Simoneau, Tracie A. Barnett, Vicky Drapeau, Marie-Ève Mathieu, Belinda Nicolau, Thibaut Varin, André Marette
P1-P109
EFFICIENCY OF ALPHA-LIPOIC ACID IN METABOLIC SYNDROMETREATMENT IN CHILDREN
Olena Tolstikova, Sergey Agarkov
EFFICIENCY OF ALPHA-LIPOIC ACID IN METABOLIC SYNDROMETREATMENT IN CHILDREN
Olena Tolstikova, Sergey Agarkov
P1-P110
Lipid accumulation product is a predictor of non-alcoholic fatty liver disease in childhood obesity
Bahar Ozcabi, Salih Demirhan, Mesut Akyol, Hatice Ozturkmen Akay, Ayla Guven
Lipid accumulation product is a predictor of non-alcoholic fatty liver disease in childhood obesity
Bahar Ozcabi, Salih Demirhan, Mesut Akyol, Hatice Ozturkmen Akay, Ayla Guven
P1-P111
Selected serum adipokines in children with irritable bowel syndrome
Joanna Oświęcimska, Agnieszka Szymlak, Agata Chobot, Bogdan Mazur, Katarzyna Ziora
Selected serum adipokines in children with irritable bowel syndrome
Joanna Oświęcimska, Agnieszka Szymlak, Agata Chobot, Bogdan Mazur, Katarzyna Ziora
P1-P112
Role of urinary NGAL and KIM-1 as early kidney injury biomarkers in obese prepubertal children
Cosimo Giannini, Nella Polidori, Marika Bagordo, Marina Primavera, Angelika Mohn, Francesco Chiarelli
Role of urinary NGAL and KIM-1 as early kidney injury biomarkers in obese prepubertal children
Cosimo Giannini, Nella Polidori, Marika Bagordo, Marina Primavera, Angelika Mohn, Francesco Chiarelli
P1-P113
Maternal resveratrol intake during pregnancy and lactation modulates the long-term metabolic effects of maternal nutrition on offspring depending on the sex and diet
Purificación Ros-Pérez, Francisca Díaz, Alejandra Freire, Pilar Argente-Arizón, Jesús Argente, Julie A. Chowen
Maternal resveratrol intake during pregnancy and lactation modulates the long-term metabolic effects of maternal nutrition on offspring depending on the sex and diet
Purificación Ros-Pérez, Francisca Díaz, Alejandra Freire, Pilar Argente-Arizón, Jesús Argente, Julie A. Chowen
P1-P114
Intrauterine metformin exposure and offspring metabolic health at 8-years follow-up
Liv Guro Engen Hanem, Pétur Júlíusson, Sven Carlsen, Marit Cecilie Fonn, Marte Øye Vaage, Øyvind Salvesen, Rønnaug Ødegård, Eszter Vanky
Intrauterine metformin exposure and offspring metabolic health at 8-years follow-up
Liv Guro Engen Hanem, Pétur Júlíusson, Sven Carlsen, Marit Cecilie Fonn, Marte Øye Vaage, Øyvind Salvesen, Rønnaug Ødegård, Eszter Vanky
P1-P115
Greater maternal BMI early in pregnancy and excessive gestational weight gain are independently associated with adverse health outcomes in the offspring at age 7 years
José G B Derraik, Valentina Chiavaroli, Sarah A Hopkins, Janene B Biggs, Raquel O Rodrigues, Sumudu N Seneviratne, Lesley M E McCowan, Wayne S Cutfield, Paul L Hofman
Greater maternal BMI early in pregnancy and excessive gestational weight gain are independently associated with adverse health outcomes in the offspring at age 7 years
José G B Derraik, Valentina Chiavaroli, Sarah A Hopkins, Janene B Biggs, Raquel O Rodrigues, Sumudu N Seneviratne, Lesley M E McCowan, Wayne S Cutfield, Paul L Hofman
P1-P116
Rapid BMI gain during later infant accelerates skeletal maturation at prepubertal obese children
Toru Kikuchi, Keisuke Nagasaki, Yohei Ogawa, Yuki Abe, Ikuma Musha, Akira Ohtake
Rapid BMI gain during later infant accelerates skeletal maturation at prepubertal obese children
Toru Kikuchi, Keisuke Nagasaki, Yohei Ogawa, Yuki Abe, Ikuma Musha, Akira Ohtake
P1-P117
The more obese - the less pubertal height gain
Anton Holmgren, Aimon Niklasson, Julián Martínez-Villanueva, Gabriel Á Martos-Moreno, Jesús Argente, Kerstin Albertsson-Wikland
The more obese - the less pubertal height gain
Anton Holmgren, Aimon Niklasson, Julián Martínez-Villanueva, Gabriel Á Martos-Moreno, Jesús Argente, Kerstin Albertsson-Wikland
P1-P118
Longitudinal changes in abdominal fat distribution in the first two years of life
Inge van Beijsterveldt, Kirsten de Fluiter, Dennis Acton, Anita Hokken-Koelega
Longitudinal changes in abdominal fat distribution in the first two years of life
Inge van Beijsterveldt, Kirsten de Fluiter, Dennis Acton, Anita Hokken-Koelega
P1-P119
Telemedicine therapy for overweight adolescents: first results of a novel smartphone app intervention using a behavioural health platform
Katrin Heldt, Dirk Büchter, Björn Brogle, Iris Shih Chen-Hsuan, Dominik Rüegger, Andreas Filler, Pauline Gindrat, Dominique Durrer, Nathalie Farpour-Lambert, Tobias Kowatsch, Dagmar l'Allemand
Telemedicine therapy for overweight adolescents: first results of a novel smartphone app intervention using a behavioural health platform
Katrin Heldt, Dirk Büchter, Björn Brogle, Iris Shih Chen-Hsuan, Dominik Rüegger, Andreas Filler, Pauline Gindrat, Dominique Durrer, Nathalie Farpour-Lambert, Tobias Kowatsch, Dagmar l'Allemand
P1-P120
Cardiorespiratory fitness effectiveness is related to abdominal adiposity and insulin sensitivity in overweight adolescents
Tetyana Chaychenko, Olena Rybka
Cardiorespiratory fitness effectiveness is related to abdominal adiposity and insulin sensitivity in overweight adolescents
Tetyana Chaychenko, Olena Rybka
P1-P121
Promoting healthy lifestyles in youth: preliminary ffrom the CIRCUIT program
Marina Ybarra, Prince Kevin Daniels, Andraea Van Hulst, Tracie A Barnett, Marie-Ève Mathieu, Olivier Drouin, Lisa Kakinami, Jean-Luc Bigras, Mélanie Henderson
Promoting healthy lifestyles in youth: preliminary ffrom the CIRCUIT program
Marina Ybarra, Prince Kevin Daniels, Andraea Van Hulst, Tracie A Barnett, Marie-Ève Mathieu, Olivier Drouin, Lisa Kakinami, Jean-Luc Bigras, Mélanie Henderson
P1-P122
Determinants of attrition from a healthy lifestyle intervention: experience from the CIRCUIT Program
Prince Kevin Daniels, Marina Ybarra, Andrea Van Hulst, Tracie A. Barnett, Marie-Ève Mathieu, Olivier Drouin, Lisa Kakinami, Jean-Luc Bigras, Mélanie Henderson
Determinants of attrition from a healthy lifestyle intervention: experience from the CIRCUIT Program
Prince Kevin Daniels, Marina Ybarra, Andrea Van Hulst, Tracie A. Barnett, Marie-Ève Mathieu, Olivier Drouin, Lisa Kakinami, Jean-Luc Bigras, Mélanie Henderson
P1-P123
Interleukin-6 Levels are associated with high blood pressure and low HDL cholesterol in healthy 4-year-old children
Haewoon Jung, Young Ah Lee, Hye Jin Lee, Youn-Hee Lim, Yun-Chul Hong, Choong Ho Shin, Sei Won Yang
Interleukin-6 Levels are associated with high blood pressure and low HDL cholesterol in healthy 4-year-old children
Haewoon Jung, Young Ah Lee, Hye Jin Lee, Youn-Hee Lim, Yun-Chul Hong, Choong Ho Shin, Sei Won Yang
P1-P124
Metabolic phenotype of human adipocytes overexpressing UCP1
Daniel Tews, Taner Pula, Jan-Bernd Funcke, Martin Wabitsch, Pamela Fischer-Posovszky
Metabolic phenotype of human adipocytes overexpressing UCP1
Daniel Tews, Taner Pula, Jan-Bernd Funcke, Martin Wabitsch, Pamela Fischer-Posovszky
P1-P125
M2 macrophage markers are enriched in human deep neck adipose tissue and do not correlate with UCP1 expression
Daniel Tews, Benedikt Haggenmueller, Martin Wabitsch, Pamela Fischer-Posovszky
M2 macrophage markers are enriched in human deep neck adipose tissue and do not correlate with UCP1 expression
Daniel Tews, Benedikt Haggenmueller, Martin Wabitsch, Pamela Fischer-Posovszky
P1-P126
Effect of hormonal changes on exocrine pancreatic function in girls with anorexia nervosa
Małgorzata Stojewska, Żaneta Malczyk, Jarosław Kwiecień, Bogdan Mazur, Katarzyna Ziora, Joanna Oświęcimska
Effect of hormonal changes on exocrine pancreatic function in girls with anorexia nervosa
Małgorzata Stojewska, Żaneta Malczyk, Jarosław Kwiecień, Bogdan Mazur, Katarzyna Ziora, Joanna Oświęcimska
P1-P127
PCSK9 and Lp(a) levels of children born after assisted reproduction technologies
Ioanna Kosteria, Dimitrios Terentes-Printzios, Iosif Koutagiar, Charalambos Vlachopoulos, Alexandra Gkourogianni, Sophia Sakka, Ioannis Skoumas, Antigoni Miliou, Ioannis Papassotiriou, Dimitrios Loutradis, George P. Chrousos, Dimitrios Tousoulis, Christina Kanaka-Gantenbein
PCSK9 and Lp(a) levels of children born after assisted reproduction technologies
Ioanna Kosteria, Dimitrios Terentes-Printzios, Iosif Koutagiar, Charalambos Vlachopoulos, Alexandra Gkourogianni, Sophia Sakka, Ioannis Skoumas, Antigoni Miliou, Ioannis Papassotiriou, Dimitrios Loutradis, George P. Chrousos, Dimitrios Tousoulis, Christina Kanaka-Gantenbein
P1-P128
Rate of accumulation of abdominal fat is associated with fasting glucose levels in early childhood
Suresh Anand Sadananthan, Mya Thway Tint, Navin Michael, Wei Wei Pang, See Ling Loy, Shu-E Soh, Lynette Shek, Fabian Yap, Kok Hian Tan, Michael Kramer, Johan Eriksson, Keith Godfrey, Peter Gluckman, Yap Seng Chong, Neerja Karnani, Yung Seng Lee, Marielle Fortier, S. Sendhil Velan
Rate of accumulation of abdominal fat is associated with fasting glucose levels in early childhood
Suresh Anand Sadananthan, Mya Thway Tint, Navin Michael, Wei Wei Pang, See Ling Loy, Shu-E Soh, Lynette Shek, Fabian Yap, Kok Hian Tan, Michael Kramer, Johan Eriksson, Keith Godfrey, Peter Gluckman, Yap Seng Chong, Neerja Karnani, Yung Seng Lee, Marielle Fortier, S. Sendhil Velan
P1-P129
Early menarche is associated with insulin resistance and non-alcoholic fatty liver disease in obese adolescents
Anna Di Sessa, Anna Grandone, Pierluigi Marzuillo, Emanuele Miraglia del Giudice
Early menarche is associated with insulin resistance and non-alcoholic fatty liver disease in obese adolescents
Anna Di Sessa, Anna Grandone, Pierluigi Marzuillo, Emanuele Miraglia del Giudice
P1-P130
The frequency of obstructive sleep apnea in children with hypothalamic and exogenous obesity
Irem Iyigun, Ayfer Alikasifoglu, Alev Ozon, Nazli Gonc, Mina Hizal, Sanem Eryilmaz, Nural Kiper, Ugur Ozcelik
The frequency of obstructive sleep apnea in children with hypothalamic and exogenous obesity
Irem Iyigun, Ayfer Alikasifoglu, Alev Ozon, Nazli Gonc, Mina Hizal, Sanem Eryilmaz, Nural Kiper, Ugur Ozcelik
P1-P131
The importance of universal lipid profile screening in two to ten years old Lebanese children
Georges Nicolas, Simon Akiki, Marie-Claude Faddous Khalifeh, Georges Nawfal, Naim Bassil, Perla Matta
The importance of universal lipid profile screening in two to ten years old Lebanese children
Georges Nicolas, Simon Akiki, Marie-Claude Faddous Khalifeh, Georges Nawfal, Naim Bassil, Perla Matta
P1-P132
Non-invasive measurements of central blood pressure with arterial stiffness indicators as a new research tool for predicting cardiovascular risk in children with Type 1 Diabetes Mellitus and obesity
Klaudyna Noiszewska, Mateusz Puchalski, Anna Skolimowska, Prof. Artur Bossowski
Non-invasive measurements of central blood pressure with arterial stiffness indicators as a new research tool for predicting cardiovascular risk in children with Type 1 Diabetes Mellitus and obesity
Klaudyna Noiszewska, Mateusz Puchalski, Anna Skolimowska, Prof. Artur Bossowski
P1-P133
Severe obesity and Cardiometabolic Comorbidities in adolescents: chronology of an epidemic
Orit Pinhas-Hamiel, Brian Reichman, Arnon Afek, Estela Derazne, Uri Hamiel, Ariel Furer, Liron Gershovitz, Jeremy D. Kark, Tarif Bader, Gilad Twig
Severe obesity and Cardiometabolic Comorbidities in adolescents: chronology of an epidemic
Orit Pinhas-Hamiel, Brian Reichman, Arnon Afek, Estela Derazne, Uri Hamiel, Ariel Furer, Liron Gershovitz, Jeremy D. Kark, Tarif Bader, Gilad Twig
P1-P134
Evaluation of intraocular pressure and retinal nerve fiber layer, retinal ganglion cell, central macular thickness and choroidal thickness using optical coherence tomography in obese children and healthy controls
Rıza Taner Baran, Serpil Baran, Naciye Füsun Toraman, Meral Bilgilisoy Filiz, Serkan Filiz, Hüseyin Demirbilek
Evaluation of intraocular pressure and retinal nerve fiber layer, retinal ganglion cell, central macular thickness and choroidal thickness using optical coherence tomography in obese children and healthy controls
Rıza Taner Baran, Serpil Baran, Naciye Füsun Toraman, Meral Bilgilisoy Filiz, Serkan Filiz, Hüseyin Demirbilek
P2-P123
Allopurinol ameliorates non-alcoholic fatty liver disease in rats
Huseyin Anil Korkmaz, Huseyin Aktug, Dincer Atila, Vatan Barisik, Nur Arslan, Oytun Erbas
Allopurinol ameliorates non-alcoholic fatty liver disease in rats
Huseyin Anil Korkmaz, Huseyin Aktug, Dincer Atila, Vatan Barisik, Nur Arslan, Oytun Erbas
P2-P124
Relationships of dietary intake and sugar rich products consumption with hepatic fat content and insulin resistance among children with overweight/obesity: The PREDIKID study
Lide Aranaza, Ignacio Diez-Lopez, Maria Medrano, Maddi Oses, Inge Huybrechts, Fran B Ortega, Idoia Labayen
Relationships of dietary intake and sugar rich products consumption with hepatic fat content and insulin resistance among children with overweight/obesity: The PREDIKID study
Lide Aranaza, Ignacio Diez-Lopez, Maria Medrano, Maddi Oses, Inge Huybrechts, Fran B Ortega, Idoia Labayen
P2-P125
Angiotensin-Converting enzyme insertion/deletion gene polymorphism in Egyptian obese children and adolescents: relation to hypertension risk
Rasha Hamza, Zeinab Elkabbany, Tarek Kamal, Mina Sedhom
Angiotensin-Converting enzyme insertion/deletion gene polymorphism in Egyptian obese children and adolescents: relation to hypertension risk
Rasha Hamza, Zeinab Elkabbany, Tarek Kamal, Mina Sedhom
P2-P126
Serum calprotectin level in children: marker of obesity and its metabolic complications
Valeria Calcaterra, Mara De Amici, Annalisa De Silvestri, Alexandre Michev, Chiara Montalbano, Corrado Regalbuto, Luca Maria Schiano, Hellas Cena, Daniela Larizza
Serum calprotectin level in children: marker of obesity and its metabolic complications
Valeria Calcaterra, Mara De Amici, Annalisa De Silvestri, Alexandre Michev, Chiara Montalbano, Corrado Regalbuto, Luca Maria Schiano, Hellas Cena, Daniela Larizza
P2-P127
Pediatric Continuous Metabolic Syndrome score (PsiMS score): use in everyday clinical practice
Rade Vukovic, Ivan Soldatovic, Tatjana Milenkovic, Katarina Mitrovic, Sladjana Todorovic, Ljiljana Plavsic
Pediatric Continuous Metabolic Syndrome score (PsiMS score): use in everyday clinical practice
Rade Vukovic, Ivan Soldatovic, Tatjana Milenkovic, Katarina Mitrovic, Sladjana Todorovic, Ljiljana Plavsic
P2-P128
Leptin and cytokines are not the best markers for metabolic S
Beatriz Garcia Cuartero, Amparo Gonzalez Vergaz, Concepción Garcia Lacalle, Veronica Sanchez Escudero, Laura Sanchez Salado, Carmen Hernando de Larramendi
Leptin and cytokines are not the best markers for metabolic S
Beatriz Garcia Cuartero, Amparo Gonzalez Vergaz, Concepción Garcia Lacalle, Veronica Sanchez Escudero, Laura Sanchez Salado, Carmen Hernando de Larramendi
P2-P129
Early-life risk factors and their association with hypertension in Spanish children and adolescents
Gloria Pérez-Gimeno, Azhara I. Rupérez, Mercedes Gil-Campos, Rosaura Leis, Concepción M. Aguilera, Ángel Gil, Luis A. Moreno, Gloria Bueno-Lozano
Early-life risk factors and their association with hypertension in Spanish children and adolescents
Gloria Pérez-Gimeno, Azhara I. Rupérez, Mercedes Gil-Campos, Rosaura Leis, Concepción M. Aguilera, Ángel Gil, Luis A. Moreno, Gloria Bueno-Lozano
P2-P130
A rare case of diabetes mellitus in an adolescent: partial lipodystrophy
Samim Özen, Aysun Ata, Damla Gökşen, Barış Akıncı, Canan Altay Tuncer, Şükran Darcan
A rare case of diabetes mellitus in an adolescent: partial lipodystrophy
Samim Özen, Aysun Ata, Damla Gökşen, Barış Akıncı, Canan Altay Tuncer, Şükran Darcan
P2-P131
Visfatin, RBP4 and STRA6 polymorphisms’ in relation with childhood obesity
Ionela Pascanu, Raluca Pop, Simona Vasilache, Oana Marginean, Valeriu Moldovan, Claudia Banescu
Visfatin, RBP4 and STRA6 polymorphisms’ in relation with childhood obesity
Ionela Pascanu, Raluca Pop, Simona Vasilache, Oana Marginean, Valeriu Moldovan, Claudia Banescu
P2-P132
CHARACTERISTICS OF BLOOD LIPIDS IN BOYS WITH HYPOANDROGENIA
Olena Budreiko, Ganna Kosovtsova, Larisa Nikitina
CHARACTERISTICS OF BLOOD LIPIDS IN BOYS WITH HYPOANDROGENIA
Olena Budreiko, Ganna Kosovtsova, Larisa Nikitina
P2-P133
Tri-Ponderal Mass Index. A good anthropometric index to evaluate adiposity in children and adolescents.
Miguel Klünder Klünder, Myrna Bravo Peregrina, Desirée López Gonzalez, Patricia Clark, América Liliana Miranda Lora
Tri-Ponderal Mass Index. A good anthropometric index to evaluate adiposity in children and adolescents.
Miguel Klünder Klünder, Myrna Bravo Peregrina, Desirée López Gonzalez, Patricia Clark, América Liliana Miranda Lora
P2-P134
Serum Spexin Concentrations in Adolescent Females with Metabolic Syndrome, Polycystic Ovary Syndrome and Anorexia Nervosa
Flora Bacopoulou, Vasiliki Efthymiou, Despoina Apostolaki, Christina Tsitsimpikou, Konstantinos Tsarouhas, Christina Darviri, Aimilia Mantzou
Serum Spexin Concentrations in Adolescent Females with Metabolic Syndrome, Polycystic Ovary Syndrome and Anorexia Nervosa
Flora Bacopoulou, Vasiliki Efthymiou, Despoina Apostolaki, Christina Tsitsimpikou, Konstantinos Tsarouhas, Christina Darviri, Aimilia Mantzou
P2-P135
A SIMPLE RELAXATION EXERCISE REDUCES STRESS IN OBESE YOUTH - A PATH TO A HEALTHY LIFESTYLE?
Aikaterini Stasinaki, Dirk Büchter, C.-H. I. Shih, Katrin Heldt, Catherine White, Dominic Rüegger, Andreas Filler, Pauline Gindrat, Dominique Durrer, Björn Brogle, Nathalie Farpour-Lambert, Tobias Kowatsch, Dagmar L’Allemand
A SIMPLE RELAXATION EXERCISE REDUCES STRESS IN OBESE YOUTH - A PATH TO A HEALTHY LIFESTYLE?
Aikaterini Stasinaki, Dirk Büchter, C.-H. I. Shih, Katrin Heldt, Catherine White, Dominic Rüegger, Andreas Filler, Pauline Gindrat, Dominique Durrer, Björn Brogle, Nathalie Farpour-Lambert, Tobias Kowatsch, Dagmar L’Allemand
P2-P136
Dyslipidemia and its related factors in Chinese children and adolescents with Turner Syndrome
Siqi Huang, Hongshan Chen, Minlian Du, Yanhong Li, Huamei Ma, Qiuli Chen, Jun Zhang, Song Guo
Dyslipidemia and its related factors in Chinese children and adolescents with Turner Syndrome
Siqi Huang, Hongshan Chen, Minlian Du, Yanhong Li, Huamei Ma, Qiuli Chen, Jun Zhang, Song Guo
P2-P137
Severity, duration and phenotype of obesity promote precocious cardiovascular sonographic alterations in childhood obesity
Domenico Corica, Tommaso Aversa, Lilia Oreto, Maria Pia Calabrò, Luca Longobardo, Marta Catalfamo, Angela Alibrandi, Filippo De Luca, Malgorzata Wasniewska
Severity, duration and phenotype of obesity promote precocious cardiovascular sonographic alterations in childhood obesity
Domenico Corica, Tommaso Aversa, Lilia Oreto, Maria Pia Calabrò, Luca Longobardo, Marta Catalfamo, Angela Alibrandi, Filippo De Luca, Malgorzata Wasniewska
P2-P138
Physical activity determined by accelerometry before and after an integral treatment program in children with abdominal obesity
María Cristina Azcona, Lydia Morell, Amaia Ochotorena, Ojeda Ana, Jose Luis Leon, Monica Prados, María Chueca, Amelia Marti, Other members Grupo GenoI
Physical activity determined by accelerometry before and after an integral treatment program in children with abdominal obesity
María Cristina Azcona, Lydia Morell, Amaia Ochotorena, Ojeda Ana, Jose Luis Leon, Monica Prados, María Chueca, Amelia Marti, Other members Grupo GenoI
P2-P139
The associations between neck – and upper arm circumference with cardiometabolic risk over traditional risk factors in adolescents - data from five European countries (PreSTART-study)
Susann Weihrauch-Blüher, David Petroff, Emer M. Brady, Laura J. Gray, Rogério T. Ribeiro, I. Vergara Mitxeltorena, Diana A. Gerasimidi-Vazeou, Melanie .J. Davies
The associations between neck – and upper arm circumference with cardiometabolic risk over traditional risk factors in adolescents - data from five European countries (PreSTART-study)
Susann Weihrauch-Blüher, David Petroff, Emer M. Brady, Laura J. Gray, Rogério T. Ribeiro, I. Vergara Mitxeltorena, Diana A. Gerasimidi-Vazeou, Melanie .J. Davies
P2-P140
Sex-related differences and effect of puberty on Metabolic Syndrome in obese children and adolescents
Chiara Guzzetti, Anastasia Ibba, Letizia Casula, Sabrina Pilia, Sandro Loche
Sex-related differences and effect of puberty on Metabolic Syndrome in obese children and adolescents
Chiara Guzzetti, Anastasia Ibba, Letizia Casula, Sabrina Pilia, Sandro Loche
P2-P141
Associations between total leptin, bio-inactive leptin, soluble leptin receptor and anthropometrics in children with severe early-onset obesity (SEOO) – the German-Polish Study (EOL-GPS)
Agnieszka Zachurzok, Ewa Malecka-Tendera, Elzbieta Petriczko, Artur Mazur, Lutz Pridzun, Bertram Flehmig, Julia von Schnurbein, Michael B. Ranke, Martin Wabitsch, Stephanie Brandt
Associations between total leptin, bio-inactive leptin, soluble leptin receptor and anthropometrics in children with severe early-onset obesity (SEOO) – the German-Polish Study (EOL-GPS)
Agnieszka Zachurzok, Ewa Malecka-Tendera, Elzbieta Petriczko, Artur Mazur, Lutz Pridzun, Bertram Flehmig, Julia von Schnurbein, Michael B. Ranke, Martin Wabitsch, Stephanie Brandt
P2-P142
Children with obesity are taller in early childhood with subsequent catch-down growth until adolescence
Elena Kempf, Tim Vogel, Jürgen Kratzsch, Mandy Vogel, Kathrin Landgraf, Elena Sergeyev, Wieland Kiess, Juraj Stanik, Antje Körner
Children with obesity are taller in early childhood with subsequent catch-down growth until adolescence
Elena Kempf, Tim Vogel, Jürgen Kratzsch, Mandy Vogel, Kathrin Landgraf, Elena Sergeyev, Wieland Kiess, Juraj Stanik, Antje Körner
P2-P143
The relationship between anthropometric measurements and breast milk ghrelin and nesfatin-1 levels in infants with small for gestational age
Berna Eroğlu Filibeli, Melike Karabulut, Saliha Aksun, Gönül Çatlı, Bumin Nuri Dündar
The relationship between anthropometric measurements and breast milk ghrelin and nesfatin-1 levels in infants with small for gestational age
Berna Eroğlu Filibeli, Melike Karabulut, Saliha Aksun, Gönül Çatlı, Bumin Nuri Dündar
P2-P144
Efficacy, safety and tolerability of Liraglutide, GLP-1 Analogue, in Indian adolescent population with obesity
Aashish Sethi, Smita Ramachandran, Inderpal Kochar
Efficacy, safety and tolerability of Liraglutide, GLP-1 Analogue, in Indian adolescent population with obesity
Aashish Sethi, Smita Ramachandran, Inderpal Kochar
P2-P145
The effect of exclusive breastfeeding and formula feeding on body composition during the first two years of life
Kirsten de Fluiter, Dennis Acton, Anita Hokken-Koelega
The effect of exclusive breastfeeding and formula feeding on body composition during the first two years of life
Kirsten de Fluiter, Dennis Acton, Anita Hokken-Koelega
P2-P146
Body composition and cardiovascular function in pre-adolescent children of South Asian and White European origin: Relationship to maternal status in pregnancy.
Andrew Whatmore, Sophia Khan, Avni Vyas, Michael Maresh, Kennedy Cruickshank, Peter Clayton
Body composition and cardiovascular function in pre-adolescent children of South Asian and White European origin: Relationship to maternal status in pregnancy.
Andrew Whatmore, Sophia Khan, Avni Vyas, Michael Maresh, Kennedy Cruickshank, Peter Clayton
P2-P147
Relation between cardiac function and anthropometric parameters in overweight and obese school boys
Viktoriya Furdela, Halyna Pavlyshyn
Relation between cardiac function and anthropometric parameters in overweight and obese school boys
Viktoriya Furdela, Halyna Pavlyshyn
P2-P148
Evaluation of hydration status of obese children - a pilot study
Celik Akif, Cebeci Ayse Nurcan
Evaluation of hydration status of obese children - a pilot study
Celik Akif, Cebeci Ayse Nurcan
P2-P149
Galanin is positively correlated with insulin resistance and triglyceride levels in obese children
Sezer Acar, Ahu Paketçi, Tuncay Küme, Korcan Demir, Özlem Gürsoy Çalan, Ece Böber, Ayhan Abacı
Galanin is positively correlated with insulin resistance and triglyceride levels in obese children
Sezer Acar, Ahu Paketçi, Tuncay Küme, Korcan Demir, Özlem Gürsoy Çalan, Ece Böber, Ayhan Abacı
P2-P150
Brown adipose tissue in prepubertal children: associations with sex and with the sequence of prenatal growth restraint and postnatal catch-up
Rita Malpique, José Miguel Gallego-Escuredo, Giorgia Sebastiani, Joan Villarroya, Abel López-Bermejo, Francis de Zegher, Francesc Villarroya, Lourdes Ibáñez
Brown adipose tissue in prepubertal children: associations with sex and with the sequence of prenatal growth restraint and postnatal catch-up
Rita Malpique, José Miguel Gallego-Escuredo, Giorgia Sebastiani, Joan Villarroya, Abel López-Bermejo, Francis de Zegher, Francesc Villarroya, Lourdes Ibáñez
P2-P151
The age of pubertal onset correlates with pubertal growth pattern and body weight change in girls
Yan-Hong Li, Min-Lian Du, Hua-Mei Ma
The age of pubertal onset correlates with pubertal growth pattern and body weight change in girls
Yan-Hong Li, Min-Lian Du, Hua-Mei Ma
P2-P152
Does late sleeping time results increased bedtime snack? What is the risk of this in childhood obesity?
Mehmet Mustafa Yılmaz, Fatih Günay, Nisa Eda Çullas İlarslan, Özlem Yılmaz, Funda Seher Özalp Ateş, Serdal Kenan Köse, Semra Atalay, Pelin Bilir
Does late sleeping time results increased bedtime snack? What is the risk of this in childhood obesity?
Mehmet Mustafa Yılmaz, Fatih Günay, Nisa Eda Çullas İlarslan, Özlem Yılmaz, Funda Seher Özalp Ateş, Serdal Kenan Köse, Semra Atalay, Pelin Bilir
P2-P153
Early BMI trajectory classes are linked to distinct body fat partitioning later in childhood
Navin Michael, Ong Yi Ying, Suresh Anand Sadananthan, Izzuddin M Aris, Mya Thway Tint, Wen Yuan Lun, Pang Wei Wei, Loy See Ling, Shu-E Soh, Lynette Pei-Chi Shek, Fabian Kok Peng Yap, Kok Hian Tan, Keith M. Godfrey, Peter D. Gluckman, Yap Seng Chong, Neerja Karnani, Michael S. Kramer, Johan G. Eriksson, Marielle V. Fortier, S. Sendhil Velan, Yung Seng Lee
Early BMI trajectory classes are linked to distinct body fat partitioning later in childhood
Navin Michael, Ong Yi Ying, Suresh Anand Sadananthan, Izzuddin M Aris, Mya Thway Tint, Wen Yuan Lun, Pang Wei Wei, Loy See Ling, Shu-E Soh, Lynette Pei-Chi Shek, Fabian Kok Peng Yap, Kok Hian Tan, Keith M. Godfrey, Peter D. Gluckman, Yap Seng Chong, Neerja Karnani, Michael S. Kramer, Johan G. Eriksson, Marielle V. Fortier, S. Sendhil Velan, Yung Seng Lee
P2-P154
Hair cortisol concentrations in overweight and obese children and adolescents
Sofia Genitsaridi, Sofia Karampatsou, Ifigeneia Papageorgiou, Aimilia Mantzou, Georgios Paltoglou, Christie Kourkouti, Chryssanthi Papathanasiou, Penio Kassari, Nicolas C. Nicolaides, Evangelia Charmandari
Hair cortisol concentrations in overweight and obese children and adolescents
Sofia Genitsaridi, Sofia Karampatsou, Ifigeneia Papageorgiou, Aimilia Mantzou, Georgios Paltoglou, Christie Kourkouti, Chryssanthi Papathanasiou, Penio Kassari, Nicolas C. Nicolaides, Evangelia Charmandari
P2-P155
Associations between body fat mass and internalizing and externalizing behaviors and anxiety in children and adolescents
Eirini Christaki, Despoina Bastaki, Eleni Valavani, Christina Kanaka-Gantenbein, Dario Bosciero, George Chrousos, Panagiota Pervanidou
Associations between body fat mass and internalizing and externalizing behaviors and anxiety in children and adolescents
Eirini Christaki, Despoina Bastaki, Eleni Valavani, Christina Kanaka-Gantenbein, Dario Bosciero, George Chrousos, Panagiota Pervanidou
P2-P156
Pharmacotherapy and the effects on LDL levels and growth in 2 children with severe Familial Hypercholesterolemia
Aravind Venkatesh Sreedharan, Fabian Yap KP
Pharmacotherapy and the effects on LDL levels and growth in 2 children with severe Familial Hypercholesterolemia
Aravind Venkatesh Sreedharan, Fabian Yap KP
P2-P157
Brown tumors in children on hemodialysis
Polina Miteva, Dimitar Roussinov, Kremena Dimitrova, Russka Shumnalieva
Brown tumors in children on hemodialysis
Polina Miteva, Dimitar Roussinov, Kremena Dimitrova, Russka Shumnalieva
P2-P158
The role of Fibroblast Growth Factor 21 and Irisin in the pathogenesis of obesity in childhood and adolescence
Sofia-Iliada Karampatsou, Sofia-Maria Genitsaridi, Ifigeneia Papageorgiou, Evangelia Charmandari
The role of Fibroblast Growth Factor 21 and Irisin in the pathogenesis of obesity in childhood and adolescence
Sofia-Iliada Karampatsou, Sofia-Maria Genitsaridi, Ifigeneia Papageorgiou, Evangelia Charmandari
P2-P159
Serum NAMPT levels are not associated with parameters of liver function in children and adolescents
Melanie Penke, Susanne Schuster, Yvonne Dietz, Antje Garten, Nico Grafe, Thomas Karlas, Johannes Wiegand, Antje Körner, Wieland Kiess
Serum NAMPT levels are not associated with parameters of liver function in children and adolescents
Melanie Penke, Susanne Schuster, Yvonne Dietz, Antje Garten, Nico Grafe, Thomas Karlas, Johannes Wiegand, Antje Körner, Wieland Kiess
P2-P160
Obesogenic environment and their influence on adiposity on Mexican children and adolescents
DESIREE LOPEZ-GONZALEZ, JONATHAN WELLS, PAMELA Reyes-Delpech, FATIMA Avila-Rosano, MARCELA Ortiz-Obregon, FRIDA Gomez-Mendoza, PATRICIA CLARK
Obesogenic environment and their influence on adiposity on Mexican children and adolescents
DESIREE LOPEZ-GONZALEZ, JONATHAN WELLS, PAMELA Reyes-Delpech, FATIMA Avila-Rosano, MARCELA Ortiz-Obregon, FRIDA Gomez-Mendoza, PATRICIA CLARK
P2-P161
Metabolic alterations and weight status in children at 8 years: a prospective cohort study
Isolina Riaño-Galán, Ana Fernández-Somoano, Cristina Rodriguez-Dehli, Rafael Venta Obaya, Adonina Tardon
Metabolic alterations and weight status in children at 8 years: a prospective cohort study
Isolina Riaño-Galán, Ana Fernández-Somoano, Cristina Rodriguez-Dehli, Rafael Venta Obaya, Adonina Tardon
P2-P162
Correlation of dietary habits with systolic blood pressure in healthy children
Maria Efthymia Katsa, Maria Batsikoura, Loukia Dolianiti, Vasileios Vasilopoulos, Dafni Eleni Kougioumtzi Dimoliani, Ioannis Dimopoulos, Andreea Paola Rojas Gil
Correlation of dietary habits with systolic blood pressure in healthy children
Maria Efthymia Katsa, Maria Batsikoura, Loukia Dolianiti, Vasileios Vasilopoulos, Dafni Eleni Kougioumtzi Dimoliani, Ioannis Dimopoulos, Andreea Paola Rojas Gil
P2-P163
Evaluation of voiding dysfunction in obese children
Havva Nur Asilturk, Bayram Ozhan, Selcuk Yuksel
Evaluation of voiding dysfunction in obese children
Havva Nur Asilturk, Bayram Ozhan, Selcuk Yuksel
P2-P164
Comparison of antropometric and biochemical parameters in obese children with or without primary headache
ONUR AKIN, MUTLUAY ARSLAN
Comparison of antropometric and biochemical parameters in obese children with or without primary headache
ONUR AKIN, MUTLUAY ARSLAN
P2-P165
The protective effect of exclusive breastfeeding for overweight / obesity in children with high birth weight
Hae Soon Kim, Jung Won Lee, Myeongjee Lee, Eun-Hee Ha, Young Ju Kim
The protective effect of exclusive breastfeeding for overweight / obesity in children with high birth weight
Hae Soon Kim, Jung Won Lee, Myeongjee Lee, Eun-Hee Ha, Young Ju Kim
P2-P166
Determinants and consequences of exaggerated adrenarche in simple obesity
Jean De Schepper, Jesse Vanbesien, Stephanie Verheyden, Ellen Anckaert, Inge Gies
Determinants and consequences of exaggerated adrenarche in simple obesity
Jean De Schepper, Jesse Vanbesien, Stephanie Verheyden, Ellen Anckaert, Inge Gies
P2-P167
Metabolic alteration in patients affected by PseudoHypoParathyroidismo 1a (PHP1a): a preliminary data
danilo FINTINI, Graziamaria Ubertini, Giuseppe Scirè, Alessio Covertino, Sarah Bocchini, Annalisa Deodati, Marco Cappa
Metabolic alteration in patients affected by PseudoHypoParathyroidismo 1a (PHP1a): a preliminary data
danilo FINTINI, Graziamaria Ubertini, Giuseppe Scirè, Alessio Covertino, Sarah Bocchini, Annalisa Deodati, Marco Cappa
P2-P168
Weight loss outcomes in two-year multidisciplinary lifestyle intervention program involving obese children and their parents
Nevena Krnic, Anita Spehar Uoic, Ana Bogdanic, Katja Dumic Kubat, Eva Pavic, Natasa Rojnic Putarek
Weight loss outcomes in two-year multidisciplinary lifestyle intervention program involving obese children and their parents
Nevena Krnic, Anita Spehar Uoic, Ana Bogdanic, Katja Dumic Kubat, Eva Pavic, Natasa Rojnic Putarek
P2-P169
Relationship between glucose and lipid metabolism, inflammatory factors and adipokines in children with obesity
Ruimin Chen, Qian Ouyang, Xin Yuan, Zhuanzhuan Ai, Chunyan Cai, Xiangquan Lin, Ying Zhang, Xiaohong Yang
Relationship between glucose and lipid metabolism, inflammatory factors and adipokines in children with obesity
Ruimin Chen, Qian Ouyang, Xin Yuan, Zhuanzhuan Ai, Chunyan Cai, Xiangquan Lin, Ying Zhang, Xiaohong Yang
P2-P170
Development of resistance to Sorafenib®, a multikinase inhibitor, in hepatocellular carcinoma is mediated by SIRT
Antje Garten, Theresa Grohmann, Anja Barnikol-Oettler, Katharina Kluckova, Gareth Lavery, Wieland Kiess, Melanie Penke
Development of resistance to Sorafenib®, a multikinase inhibitor, in hepatocellular carcinoma is mediated by SIRT
Antje Garten, Theresa Grohmann, Anja Barnikol-Oettler, Katharina Kluckova, Gareth Lavery, Wieland Kiess, Melanie Penke
P2-P171
Gender and pubertal tendencies of plasma leptin and dopamine levels depending on TaqIA DRD2 gene polymorphism in the different pediatric obesity classes
Liudmila Viazava, Anzhalika Solntsava, Alena Aksionava, Alena Dashkevich
Gender and pubertal tendencies of plasma leptin and dopamine levels depending on TaqIA DRD2 gene polymorphism in the different pediatric obesity classes
Liudmila Viazava, Anzhalika Solntsava, Alena Aksionava, Alena Dashkevich
P2-P172
Iron metabolism disorders in prepubertal obese children with and without NAFLD
Cosimo Giannini, Nella Polidori, Marina Primavera, Marika Bagordo, Angelika Mohn, Francesco Chiarelli
Iron metabolism disorders in prepubertal obese children with and without NAFLD
Cosimo Giannini, Nella Polidori, Marina Primavera, Marika Bagordo, Angelika Mohn, Francesco Chiarelli
P2-P173
Familial hypercholesterolemia due to homozygous LDLRAP1 mutation: variability of phenotype and response to medical therapy
Evangelia Panou, Johannes Schumacher, Joachim Woelfle
Familial hypercholesterolemia due to homozygous LDLRAP1 mutation: variability of phenotype and response to medical therapy
Evangelia Panou, Johannes Schumacher, Joachim Woelfle
P2-P174
CAN TRIPONDERAL MASS INDEX BE A NEW INDICATOR IN THE PREDICTING CARDIOMETABOLIC RISK IN OBESE ADOLESCENTS?
Gülten Cingöz, Berna Eroğlu Filibeli, Bumin Nuri Dündar, Gönül Çatlı
CAN TRIPONDERAL MASS INDEX BE A NEW INDICATOR IN THE PREDICTING CARDIOMETABOLIC RISK IN OBESE ADOLESCENTS?
Gülten Cingöz, Berna Eroğlu Filibeli, Bumin Nuri Dündar, Gönül Çatlı
P2-P175
Social Networks, Social Support and Weight-Related Outcomes among Adolescents
Marina Ybarra, Jennifer Yu, Lisa Kakinami, Marie-Ève Mathieu, Mélanie Henderson, Tracie Barnett
Social Networks, Social Support and Weight-Related Outcomes among Adolescents
Marina Ybarra, Jennifer Yu, Lisa Kakinami, Marie-Ève Mathieu, Mélanie Henderson, Tracie Barnett
P2-P176
Identification of A Novel Homozygous Mutation in BBS10 in Five Children With Bardet-Biedl Syndrome
GULAY CAN YILMAZ, Ece Keskin, Elif Söbü
Identification of A Novel Homozygous Mutation in BBS10 in Five Children With Bardet-Biedl Syndrome
GULAY CAN YILMAZ, Ece Keskin, Elif Söbü
P2-P177
THE EFFECTS OF THE BIRTH WEIGHT ON THE FAT DISTRIBUTION AND FATNESS PARAMETERS OF THE BODY
Nihal Hatipoğlu, Gül Direk, Merve Nur Hepokur, Zeynep Uzan Tatlı, Betul Çiçek, Demet Unalan, M. Mumtaz Mazıcıoğlu, Ahmet Öztürk, Selim Kurtoğlu
THE EFFECTS OF THE BIRTH WEIGHT ON THE FAT DISTRIBUTION AND FATNESS PARAMETERS OF THE BODY
Nihal Hatipoğlu, Gül Direk, Merve Nur Hepokur, Zeynep Uzan Tatlı, Betul Çiçek, Demet Unalan, M. Mumtaz Mazıcıoğlu, Ahmet Öztürk, Selim Kurtoğlu
P2-P178
Oxidative homeostasis dysregulation may promote pathogenesis of cardio-metabolic complications in childhood obesity
Domenico Corica, Tommaso Aversa, Rosaria Maddalena Ruggeri, Mariateresa Cristani, Ilenia Panasiti, Filippo De Luca, Malgorzata Wasniewska
Oxidative homeostasis dysregulation may promote pathogenesis of cardio-metabolic complications in childhood obesity
Domenico Corica, Tommaso Aversa, Rosaria Maddalena Ruggeri, Mariateresa Cristani, Ilenia Panasiti, Filippo De Luca, Malgorzata Wasniewska
P2-P179
Body composition parameters, systemic inflammation and metabolic syndrome manifestations in children and adolescents
Eirini Christaki, Panagiota Pervanidou, Despoina Bastaki, Eleni Valavani, Christina Kanaka-Gantenbein, Dario Boschiero, Chrousos George
Body composition parameters, systemic inflammation and metabolic syndrome manifestations in children and adolescents
Eirini Christaki, Panagiota Pervanidou, Despoina Bastaki, Eleni Valavani, Christina Kanaka-Gantenbein, Dario Boschiero, Chrousos George
P2-P180
Relationships between obesity parameters and urinary concentrations of phthalates and phenols in Korean girls
Shin-Hye Kim, Man Ho Choi, Youngmin Hong, Mi-Jung Park
Relationships between obesity parameters and urinary concentrations of phthalates and phenols in Korean girls
Shin-Hye Kim, Man Ho Choi, Youngmin Hong, Mi-Jung Park
P3-P125
NKX2-2 human mutation causes neonatal diabetes followed by severe infantile obesity associated with paradoxical upregulated ghrelin levels – do beta-cells secrete ghrelin?
Adi Auerbach, Amitay Cohen, Eran Lavi, Najwa Abdulhaq, Ariella Weinberg Shokrun, Ephrat Levy-Lahad, Rina Hemi, Zangen David
NKX2-2 human mutation causes neonatal diabetes followed by severe infantile obesity associated with paradoxical upregulated ghrelin levels – do beta-cells secrete ghrelin?
Adi Auerbach, Amitay Cohen, Eran Lavi, Najwa Abdulhaq, Ariella Weinberg Shokrun, Ephrat Levy-Lahad, Rina Hemi, Zangen David
P3-P126
Tracing the effect of the Melanocortin-4 Receptor pathway in obesity: study design and methodology of the TEMPO Registry
Ihuoma Eneli, Jinyu Xu, Fred Fiedorek, Matthew Webster, Amy McCagg, Kristin Ayers, Lex Van Der Ploeg, Alastair Garfield, Elizabeth Estrada
Tracing the effect of the Melanocortin-4 Receptor pathway in obesity: study design and methodology of the TEMPO Registry
Ihuoma Eneli, Jinyu Xu, Fred Fiedorek, Matthew Webster, Amy McCagg, Kristin Ayers, Lex Van Der Ploeg, Alastair Garfield, Elizabeth Estrada
P3-P127
BigO: big data against childhood obesity
Christos Diou, Ioannis Ioakeimidis, Evangelia Charmandari, Penio Kassari, Irini Lekka, Monica Mars, Cecilia Bergh, Tahar Kechadi, Gerardine Doyle, Grace O'Malley, Rachel Heimeier, Anna Karin Lindroos, Sofoklis Sotiriou, Evangelia Koukoula, Sergio Guillén, George Lymperopoulos, Nicos Maglaveras, Anastasios Delopoulos
BigO: big data against childhood obesity
Christos Diou, Ioannis Ioakeimidis, Evangelia Charmandari, Penio Kassari, Irini Lekka, Monica Mars, Cecilia Bergh, Tahar Kechadi, Gerardine Doyle, Grace O'Malley, Rachel Heimeier, Anna Karin Lindroos, Sofoklis Sotiriou, Evangelia Koukoula, Sergio Guillén, George Lymperopoulos, Nicos Maglaveras, Anastasios Delopoulos
P3-P128
Exposure to bisphenol-A and phtalates in obese girls
Annalisa Deodati, Giorgia Bottaro, Danilo Fintini, Sabrina Tait, Francesca Maranghi, Luca Busani, Cinzia La Rocca, Roberta Tassinari, Fabrizia Carli, Veronica Della Latta, Emma Buzzigoli, Amalia Gastaldelli, Stefano Cianfarani
Exposure to bisphenol-A and phtalates in obese girls
Annalisa Deodati, Giorgia Bottaro, Danilo Fintini, Sabrina Tait, Francesca Maranghi, Luca Busani, Cinzia La Rocca, Roberta Tassinari, Fabrizia Carli, Veronica Della Latta, Emma Buzzigoli, Amalia Gastaldelli, Stefano Cianfarani
P3-P129
Obesity of childhood and ambulatory glucose monitorization
Ayça Törel Ergür, Berrin Atmaca, Tuğçe Ataseven Emeksiz
Obesity of childhood and ambulatory glucose monitorization
Ayça Törel Ergür, Berrin Atmaca, Tuğçe Ataseven Emeksiz
P3-P130
Familial Partial Lipodystrophy, importance of family history - a case report
Camilla Stockley, Susan Holder, Jayanti Rangasami
Familial Partial Lipodystrophy, importance of family history - a case report
Camilla Stockley, Susan Holder, Jayanti Rangasami
P3-P131
Development of severe obesity in a children with a brainstem tumor
Catherine Pihoker, Christian Roth
Development of severe obesity in a children with a brainstem tumor
Catherine Pihoker, Christian Roth
P3-P132
Correlation between obesity, body mass index and insulin resistance in Bulgarian children
Desislava Yordanova, Elisaveta Stefanova, Krasimira Kazakova, Zdravka Todorova, Mihaela Dimitrova, Mila Baycheva
Correlation between obesity, body mass index and insulin resistance in Bulgarian children
Desislava Yordanova, Elisaveta Stefanova, Krasimira Kazakova, Zdravka Todorova, Mihaela Dimitrova, Mila Baycheva
P3-P134
Metabolic parameters in children with syndromic obesity
Elena Sukarova-Angelovska, Mirjana Kocova, Marina Krstevska-Konstantinova, Natalija Angelkova, Tatjana Zorcec
Metabolic parameters in children with syndromic obesity
Elena Sukarova-Angelovska, Mirjana Kocova, Marina Krstevska-Konstantinova, Natalija Angelkova, Tatjana Zorcec
P3-P135
Cut-off for the follow-up of obese children: cynicism or realism?
Francesco Gallo, Giuditta De Quarto, Antonella Lonero, Fulvio Moramarco
Cut-off for the follow-up of obese children: cynicism or realism?
Francesco Gallo, Giuditta De Quarto, Antonella Lonero, Fulvio Moramarco
P3-P136
Proximal Microdelection 16p11.2 Syndrome
Francesco Leo, Simona Filomena Madeo, Alessandro Baraldi, Barbara Predieri, Ilaria Stanghellini, Olga Calabrese, Lorenzo Iughetti
Proximal Microdelection 16p11.2 Syndrome
Francesco Leo, Simona Filomena Madeo, Alessandro Baraldi, Barbara Predieri, Ilaria Stanghellini, Olga Calabrese, Lorenzo Iughetti
P3-P137
The level of the Vitamin D and metabolic status in children with obesity
Hanna Mikhno, Anzhalika Solntsava, Helena Dashkevich
The level of the Vitamin D and metabolic status in children with obesity
Hanna Mikhno, Anzhalika Solntsava, Helena Dashkevich
P3-P138
A compound heterozygote mutation in a Chinese patient affected with Methylmalonic acidemia
YU YANG, Hui Huang, Yi Yuan
A compound heterozygote mutation in a Chinese patient affected with Methylmalonic acidemia
YU YANG, Hui Huang, Yi Yuan
P3-P139
Lymposomal acid lipase deficit in patients with hypercholesterolemia
Ignacio Diez-Lopez, Ainhoa Sarasua, Isabel Lorente
Lymposomal acid lipase deficit in patients with hypercholesterolemia
Ignacio Diez-Lopez, Ainhoa Sarasua, Isabel Lorente
P3-P140
Hepatic Steatosis and its relationship with the metabolic syndrome
MARIA ANGELES SANTOS MATA, IRENE PILAR FERNANDEZ VISERAS
Hepatic Steatosis and its relationship with the metabolic syndrome
MARIA ANGELES SANTOS MATA, IRENE PILAR FERNANDEZ VISERAS
P3-P141
Serum hepcidin and ferritin in prepubertal obese children
Joanna Gajewska, Witold Klemarczyk, Jadwiga Ambroszkiewicz, Ewa Głąb-Jabłońska, Magdalena Chełchowska
Serum hepcidin and ferritin in prepubertal obese children
Joanna Gajewska, Witold Klemarczyk, Jadwiga Ambroszkiewicz, Ewa Głąb-Jabłońska, Magdalena Chełchowska
P3-P142
Osse Registry for patients with Lipodystrophy run by the European Consortium of Lipodystrophy (ECLip)
Julia von Schnurbein, Jannik Schaaf, Giovanni Cecarini, Marie-Christine Vantyghem, Camille Vatier, Gabriele Nagel, David Araujo-Vilar, Martin Wabitsch
Osse Registry for patients with Lipodystrophy run by the European Consortium of Lipodystrophy (ECLip)
Julia von Schnurbein, Jannik Schaaf, Giovanni Cecarini, Marie-Christine Vantyghem, Camille Vatier, Gabriele Nagel, David Araujo-Vilar, Martin Wabitsch
P3-P143
Acanthosis nigricans in obese children and adolescents in relation to severity of obesity and insulin resistance.
Kyung Hee Park, Hyun Jung Lim, Yoon Myoung Kim
Acanthosis nigricans in obese children and adolescents in relation to severity of obesity and insulin resistance.
Kyung Hee Park, Hyun Jung Lim, Yoon Myoung Kim
P3-P144
Serum uric acid and its correlation with metabolic syndrome factors in simple obesity children
ZULIN LIU, LIYANG LIANG, ZHE MENG, LELE HOU, LINA ZHANG, ZHUANNAN JIANG
Serum uric acid and its correlation with metabolic syndrome factors in simple obesity children
ZULIN LIU, LIYANG LIANG, ZHE MENG, LELE HOU, LINA ZHANG, ZHUANNAN JIANG
P3-P145
Thyroid function, lipid profile and carbohydrate metabolism parameters in patients with Alstrom syndrome.
Maja Okońska, Agnieszka Brandt, Małgorzata Myśliwiec
Thyroid function, lipid profile and carbohydrate metabolism parameters in patients with Alstrom syndrome.
Maja Okońska, Agnieszka Brandt, Małgorzata Myśliwiec
P3-P146
Does the level of studies of parents influence the follow-up of the recommendations of the nutritional pyramid?
María Rosaura Leis Trabazo, Carmela de Lamas Pérez, Rocío Vázquez Cobela, Juan José Bedoya Carpente, Josune Olza Meneses, Ángel Gil Hernández, Luis Alberto Moreno Aznar, Gloria Bueno Lozano, Mercedes Gil Campos, Concepción Aguilera García
Does the level of studies of parents influence the follow-up of the recommendations of the nutritional pyramid?
María Rosaura Leis Trabazo, Carmela de Lamas Pérez, Rocío Vázquez Cobela, Juan José Bedoya Carpente, Josune Olza Meneses, Ángel Gil Hernández, Luis Alberto Moreno Aznar, Gloria Bueno Lozano, Mercedes Gil Campos, Concepción Aguilera García
P3-P147
Bariatric surgery as treatment of primary Pseudotumor cerebriin a male adolescent: case report
Marina Ybarra, Tiago Jeronimo dos Santos, Edjane Santos Queiroz, Ludmilla Rachid, Ruth Rocha Franco, Louise Cominato, Frederico Castelo Moura, Manoel Carlos Velhote, Durval Damiani
Bariatric surgery as treatment of primary Pseudotumor cerebriin a male adolescent: case report
Marina Ybarra, Tiago Jeronimo dos Santos, Edjane Santos Queiroz, Ludmilla Rachid, Ruth Rocha Franco, Louise Cominato, Frederico Castelo Moura, Manoel Carlos Velhote, Durval Damiani
P3-P148
Investigation of pubertal effect on thyroid volume and IGF-1 changes in morbid obese children
Murat Karaoglan, Onur Balci, Mehmet Keskin
Investigation of pubertal effect on thyroid volume and IGF-1 changes in morbid obese children
Murat Karaoglan, Onur Balci, Mehmet Keskin
P3-P149
The effect of vitamin D supplementation on metabolic syndrome parameters in overweight and obese children and adolescents in Greece
Christos Giannios, Nicolas Nicolaides, Ioanna Farakla, Georgios Papadopoulos, Sofia Gennitsaridi, Sofia Karampatsou, Gerasimos Kolaitis, George Chrousos, Evangelia Charmandari
The effect of vitamin D supplementation on metabolic syndrome parameters in overweight and obese children and adolescents in Greece
Christos Giannios, Nicolas Nicolaides, Ioanna Farakla, Georgios Papadopoulos, Sofia Gennitsaridi, Sofia Karampatsou, Gerasimos Kolaitis, George Chrousos, Evangelia Charmandari
P3-P150
Mother's obesity and high child's waist circumference are predictive factors of severe child's obesity: an observational study in French Guiana
NJUIEYON FALUCAR, CUADRO-ALVAREZ EMMA, MARTIN ELISE, LACHAUME NOEMIE, MRSIC YAJAIRA, HENAFF FANNY, MANIASSOM CHIMENE, DEFO ANTOINE, ELENGA NARCISSE
Mother's obesity and high child's waist circumference are predictive factors of severe child's obesity: an observational study in French Guiana
NJUIEYON FALUCAR, CUADRO-ALVAREZ EMMA, MARTIN ELISE, LACHAUME NOEMIE, MRSIC YAJAIRA, HENAFF FANNY, MANIASSOM CHIMENE, DEFO ANTOINE, ELENGA NARCISSE
P3-P151
LIPIDOGRAM, LEPTIN-AND ADIPONECTINAEMIA IN TEENAGERS AND ADOLESCENTS WITH METABOLIC SYNDROM
Olena Tolstikova
LIPIDOGRAM, LEPTIN-AND ADIPONECTINAEMIA IN TEENAGERS AND ADOLESCENTS WITH METABOLIC SYNDROM
Olena Tolstikova
P3-P152
Metabolic Endotoxemia in Egyptian obese children and adolescents
Omneya Magdy Omar, Marwa Meheissen, Basma Zaki, Magdy Abd El Fattah
Metabolic Endotoxemia in Egyptian obese children and adolescents
Omneya Magdy Omar, Marwa Meheissen, Basma Zaki, Magdy Abd El Fattah
P3-P153
Resting metabolic rate and the development of metabolic disorders in obese children
Pavel Okorokov, Olga Vasyukova, Tatiana Shiryaeva, Vanentina Peterkova
Resting metabolic rate and the development of metabolic disorders in obese children
Pavel Okorokov, Olga Vasyukova, Tatiana Shiryaeva, Vanentina Peterkova
P3-P154
Relation of screen-time (phone-computer-TV-online games) and physical activity with childhood obesity
Mehmet Mustafa Yılmaz, Nisa Eda Çullas İlarslan, Fatih Günay, Özlem Yılmaz, Funda Seher Ozalp Ates, Serdal Kenan Köse, Semra Atalay, Pelin Bilir
Relation of screen-time (phone-computer-TV-online games) and physical activity with childhood obesity
Mehmet Mustafa Yılmaz, Nisa Eda Çullas İlarslan, Fatih Günay, Özlem Yılmaz, Funda Seher Ozalp Ates, Serdal Kenan Köse, Semra Atalay, Pelin Bilir
P3-P155
Effect of three-month diet and physical activity on adipokines and inflammatory status in children with metabolic syndrome
Ramona Stroescu, Otilia Marginean, Teofana Bizerea, Mihai Gafencu, Gabriela Doros
Effect of three-month diet and physical activity on adipokines and inflammatory status in children with metabolic syndrome
Ramona Stroescu, Otilia Marginean, Teofana Bizerea, Mihai Gafencu, Gabriela Doros
P3-P156
Neck circumference and lipid profile in adolescents with overweight / obesity
Ricardo Fernando Arrais, Amanda Caroline Pereira Nunes, Ana Suely de Andrade, Angélica Luíza de Sales Souza, Eduarda Pontes dos Santos Araújo, Erika Aparecida de Araújo Soares, Jéssica Bastos Pimentel, Suerda Isa Nascimento Teixeira, Thatyane Oliveira Souza, Viviane Cassia Barrionuevo Jaime, Adriana Augusto de Rezende, Severina Carla Vieira Cunha Lima
Neck circumference and lipid profile in adolescents with overweight / obesity
Ricardo Fernando Arrais, Amanda Caroline Pereira Nunes, Ana Suely de Andrade, Angélica Luíza de Sales Souza, Eduarda Pontes dos Santos Araújo, Erika Aparecida de Araújo Soares, Jéssica Bastos Pimentel, Suerda Isa Nascimento Teixeira, Thatyane Oliveira Souza, Viviane Cassia Barrionuevo Jaime, Adriana Augusto de Rezende, Severina Carla Vieira Cunha Lima
P3-P157
A not so “simple obesity”
Silvia Poluzzi, Simona Filomena Madeo, Gloria Rossi, Patrizia Bruzzi, Ilaria Stanghellini, Olga Calabrese, Lorenzo Iughetti
A not so “simple obesity”
Silvia Poluzzi, Simona Filomena Madeo, Gloria Rossi, Patrizia Bruzzi, Ilaria Stanghellini, Olga Calabrese, Lorenzo Iughetti
P3-P158
Effect of obesity on bone age and hormonal parameters in Indian children
Smita Ramachandran, Aashish Sethi, Inderpal Kochar
Effect of obesity on bone age and hormonal parameters in Indian children
Smita Ramachandran, Aashish Sethi, Inderpal Kochar
P3-P159
Compliance of obese children and their family to the directions of a Pediatric Endocrinology Medical Office
Sotiria Giannopoulou, Maria Eliopoulou, Charalampos Gogos
Compliance of obese children and their family to the directions of a Pediatric Endocrinology Medical Office
Sotiria Giannopoulou, Maria Eliopoulou, Charalampos Gogos
P3-P160
Risk factors and comorbidities of childhood obesity
Sotiria Giannopoulou, Maria Eliopoulou, Charalampos Gogos
Risk factors and comorbidities of childhood obesity
Sotiria Giannopoulou, Maria Eliopoulou, Charalampos Gogos
P3-P161
Autonomic nervous system - inflammation link: a new independent mechanism for homeostasis
STYLIANI GERONIKOLOU, GEORGE CHROUSOS, KONSTANTINOS ALBANOPOULOS, DENNIS COKKINOS, CHRISTINA KANAKA-GANTENBEIN
Autonomic nervous system - inflammation link: a new independent mechanism for homeostasis
STYLIANI GERONIKOLOU, GEORGE CHROUSOS, KONSTANTINOS ALBANOPOULOS, DENNIS COKKINOS, CHRISTINA KANAKA-GANTENBEIN
P3-P162
Effects of a brief Physician delivered counseling on childhood obesity
SUNETRA MONDAL, SUDIP CHATTERJEE
Effects of a brief Physician delivered counseling on childhood obesity
SUNETRA MONDAL, SUDIP CHATTERJEE
P3-P163
The prevalence of obesity in boys in the region of the Russian Federation
Mariya Larionova, Tatiana Kovalenko
The prevalence of obesity in boys in the region of the Russian Federation
Mariya Larionova, Tatiana Kovalenko
P3-P165
Hidden hunger in overweight/ obese Indian adolescents
Vandana Jain, Babita Upadhyaya, Anuja Agarwala
Hidden hunger in overweight/ obese Indian adolescents
Vandana Jain, Babita Upadhyaya, Anuja Agarwala
P3-P166
Assessment of obesity in children with achondroplasia and hypochondroplasia
Yukako Nakano, Taichi Kitaoka, Shinji Takeyari, Yasuhisa Ohata, Takuo Kubota, Keiichi Ozono
Assessment of obesity in children with achondroplasia and hypochondroplasia
Yukako Nakano, Taichi Kitaoka, Shinji Takeyari, Yasuhisa Ohata, Takuo Kubota, Keiichi Ozono
P3-P167
Correlation of lipoprotein(a) levels and family history of cardiovascular disease in a sample of overweight/obese children and adolescents
Kalliopi Kappou, Vasiliki Bisbinas, Zacharoula Karabouta
Correlation of lipoprotein(a) levels and family history of cardiovascular disease in a sample of overweight/obese children and adolescents
Kalliopi Kappou, Vasiliki Bisbinas, Zacharoula Karabouta
P3-P168
Beneficial effect of metformin treatment in obese children and adolescents
Zdravka Todorova, Elissaveta Stefanova, Krassimira Kazakova, Desislava Jordanova, Mihaela Dimitrova
Beneficial effect of metformin treatment in obese children and adolescents
Zdravka Todorova, Elissaveta Stefanova, Krassimira Kazakova, Desislava Jordanova, Mihaela Dimitrova
P3-P169
Comparison of the effectiveness of a battery powered and manual toothbrush in removal of a dental plaque for good oral hygiene in adolesents with over-weight
Recep Orbak, Zerrin Orbak
Comparison of the effectiveness of a battery powered and manual toothbrush in removal of a dental plaque for good oral hygiene in adolesents with over-weight
Recep Orbak, Zerrin Orbak
RFC10.3
Developmental regulation of obestatin and adropin in Prader-Willi syndrome and non-syndromic obesity: associations with weight, BMI-z, HOMA-IR, and lipid profile
Camila E Orsso, Andrew A. Butler, Michael J. Muehlbauer, Huaxia N. Cui, Daniela A. Rubin, Mohammadreza Pakseresht, Merlin G. Butler, Carla M. Prado, Michael Freemark, Andrea M. Haqq
Developmental regulation of obestatin and adropin in Prader-Willi syndrome and non-syndromic obesity: associations with weight, BMI-z, HOMA-IR, and lipid profile
Camila E Orsso, Andrew A. Butler, Michael J. Muehlbauer, Huaxia N. Cui, Daniela A. Rubin, Mohammadreza Pakseresht, Merlin G. Butler, Carla M. Prado, Michael Freemark, Andrea M. Haqq
RFC6.1
Allelic variation in key fitness genes is linked with increased severity of obesity in overweight/obese youth
Christoph Saner, Brooke E. Harcourt, Markus Juonala, Kung-Ting Kao, Peter Houweling, Fleur Garton, Kathryn N. North, Matthew A. Sabin
Allelic variation in key fitness genes is linked with increased severity of obesity in overweight/obese youth
Christoph Saner, Brooke E. Harcourt, Markus Juonala, Kung-Ting Kao, Peter Houweling, Fleur Garton, Kathryn N. North, Matthew A. Sabin
RFC6.2
IGF-I at four months associates to visceral and subcutaneous adipose tissue at 7 years of age
Emma Kjellberg, Josefine Roswall, Jonathan Andersson, Stefan Bergman, Joel Kullberg, Jovanna Dahlgren
IGF-I at four months associates to visceral and subcutaneous adipose tissue at 7 years of age
Emma Kjellberg, Josefine Roswall, Jonathan Andersson, Stefan Bergman, Joel Kullberg, Jovanna Dahlgren
RFC6.3
Effect of the Melanocortin-4 Receptor Agonist, Setmelanotide, on obesity and hyperphagia in individuals affected by Bardet-Biedl syndrome
Robert M Haws, Kristina L Fletty, Thomas J McIntee, Clayton Green, Jeremy Pomeroy, Michelle Hylan, Cathy Folster, Elisabeth K Davis, Sheila M Brady, Fred T Fiedorek, Jack A Yanovski
Effect of the Melanocortin-4 Receptor Agonist, Setmelanotide, on obesity and hyperphagia in individuals affected by Bardet-Biedl syndrome
Robert M Haws, Kristina L Fletty, Thomas J McIntee, Clayton Green, Jeremy Pomeroy, Michelle Hylan, Cathy Folster, Elisabeth K Davis, Sheila M Brady, Fred T Fiedorek, Jack A Yanovski
RFC6.4
Functionality and phenotypic characteristics of mutations in the human leptin receptor
Adriana Nunziata, Jan-Bernd Funcke, Guntram Borck, Julia von Schnurbein, Belinda Lennerz, Barbara Moepps, Peter Gierschik, Pamela Fischer-Posovszky, Martin Wabitsch
Functionality and phenotypic characteristics of mutations in the human leptin receptor
Adriana Nunziata, Jan-Bernd Funcke, Guntram Borck, Julia von Schnurbein, Belinda Lennerz, Barbara Moepps, Peter Gierschik, Pamela Fischer-Posovszky, Martin Wabitsch
RFC6.5
High-throughput untargeted plasma metabolomics unravels gender dimorphic metabolic trajectories in naturally conceived and ICSI prepubertal children
Aristeidis G. Telonis, Alexandra Gkourogianni, Ioannis Papassotiriou, Maria Konsta, Maria Papastamataki, Alexandra Margeli, Anastasia Bartzeliotou, Emilia Mantzou, Ioanna Kosteria, George Mastorakos, Dimitrios Loutradis, George P. Chrousos, Maria I. Klapa, Christina Kanaka-Gantenbein
High-throughput untargeted plasma metabolomics unravels gender dimorphic metabolic trajectories in naturally conceived and ICSI prepubertal children
Aristeidis G. Telonis, Alexandra Gkourogianni, Ioannis Papassotiriou, Maria Konsta, Maria Papastamataki, Alexandra Margeli, Anastasia Bartzeliotou, Emilia Mantzou, Ioanna Kosteria, George Mastorakos, Dimitrios Loutradis, George P. Chrousos, Maria I. Klapa, Christina Kanaka-Gantenbein
RFC6.6
EFFECTS OF CHERRY’S EXTRACT ON INCREASED OSTECLASTOGENESIS IN OBESE CHILDREN
Maria Felicia Faienza, Filomena Corbo, Alessia Carocci, Alessia Catalano, Laura Piacente, Maria Lisa Clodoveo, Sara Bortolotti, Giuseppina Storlino, Silvia Colucci, Maria Grano, Gabriele D'Amato, Giacomina Brunetti
EFFECTS OF CHERRY’S EXTRACT ON INCREASED OSTECLASTOGENESIS IN OBESE CHILDREN
Maria Felicia Faienza, Filomena Corbo, Alessia Carocci, Alessia Catalano, Laura Piacente, Maria Lisa Clodoveo, Sara Bortolotti, Giuseppina Storlino, Silvia Colucci, Maria Grano, Gabriele D'Amato, Giacomina Brunetti
Workshop
8
Oral
29
Expert
16
Plenary
8
Catering and Social
9
Nurse
1
Other
18
Symposium
21
No Session Type
5
Thu 27 09:52
WG1.6
Thu 27 08:00
WG2.1
Thu 27 08:30
WG2.2
Impaired fasting glycaemia in pediatric obesity and type 2 diabetes in young adulthood
Stockholm, Sweden
Thu 27 09:00
WG2.3
Thu 27 09:40
WG3.5
Thu 27 09:25
WG4.6
Updates on the developments of Decision Support Systems for the treatment of diabetes
Petah Tikva, Israel
Thu 27 09:45
WG4.7
Use of social media for improving glucose control in patients with type 1 diabetes
Skopje, Macedonia
Thu 27 09:10
WG5.4
Endocrine-metabolic outcome of women with a history of sexual precocity
Petah Tikva, Israel
Thu 27 09:30
WG5.5
Thu 27 08:05
WG6.1
Gender identity development: Neither male nor female or being both, growing up as gender queer
Amsterdam, The Netherlands
Thu 27 09:30
WG6.3
Fertility preservation in transgender adolescents: an ethical perspective. Is the sky the limit?
Leiden, The Netherlands
Fri 28 10:05
ERN1.3
Fri 28 10:25
ERN1.4
Fri 28 10:45
ERN1.5
EuRRECa - European Registries For Rare Endocrine Conditions
Glasgow, United Kingdom
Thu 27 15:50
FC1.6
Thu 27 15:10
FC2.2
Whole genome sequencing reveals novel intragenic deletions of GNAS as causes of pseudohypoparathyroidism type 1a.
Philadelphia, USA
Thu 27 15:20
FC2.3
Clinical course of hypoparathyroidism in patients with APECED (APS1)
Helsinki, Finland
Thu 27 15:30
FC2.4
Diagnostic Performance of Artificial Neural Network-Based TW3 Skeletal Maturity Assessment.
Hangzhou, China
Thu 27 15:40
FC2.5
Radial ESWT stimulates longitudinal bone growth in cultured rat fetal metatarsal bones.
Vellore, India
Thu 27 15:50
FC2.6
Thu 27 15:00
FC3.1
Neonatal diabetes owned to potassium channel mutation: response to sulfonylureas according to the genotype.
Paris, France)
Thu 27 15:10
FC3.2
Genome-Wide Meta-Analysis identifies a novel low frequency STK39 variant of large effect on risk of Type 1 Diabetes.
Montreal, Canada
Thu 27 15:50
FC3.6
Using CRISPR/Cas9gene editing to study the molecular genetics of Congenital Hyperinsulinism.
London, UK
Thu 27 15:00
FC4.1
Monogenic and digenic gene mutations are present in children with idiopathic short stature (ISS).
Buenos Aires, Argentina
Thu 27 15:10
FC4.2
Effects of IGF-1R nuclear localization in glioblastoma cells.
Buenos Aires, Argentina
Thu 27 15:40
FC4.5
Prediction of adult height by artificial intelligence (AI) through machine learning (ML) from early height data.
Haifa, Israel
Thu 27 15:50
FC4.6
Absorption and Excretion of Somapacitan, a Long-Acting Growth Hormone (GH) Derivative.
Søborg, Denmark
Thu 27 15:40
FC5.5
Guidelines for the Management of Paediatric Differentiated Thyroid Carcinoma; a UK endeavour.
London, UK
Thu 27 15:50
FC5.6
Alterations in DNA methylation status of gene promoters in children and adolescents with autoimmune thyroid disease.
Thessaloniki, Greece
Thu 27 16:00
RFC1.1
The relative contributions of genetic and environmental factors on cortisol metabolism at pre-, mid- and post-pubertal ages.
Amsterdam, The Netherlands
Thu 27 16:05
RFC1.2
Changes in CYP19A1 and CYP3A4 activities due to population genetic variations in human P450 Oxidoreductase.
Bern, Switzerland
Thu 27 16:15
RFC1.4
Mass spectrometry-based assessment of childhood androgen excess in 487 consecutive patients over 5 years.
Birmingham, UK
Thu 27 16:05
RFC2.2
S-25OHD is Associated with Hand Grip Strength and Myopathy at Five Years in Girls: An Odense Child Cohort Study.
Odense, Denmark
Thu 27 16:25
RFC2.6
The novel R211Q POP1 homozygous mutation causes severe short stature but uniquely only subtle skeletal dysplasia.
Hebron, Palestine
Thu 27 16:05
RFC3.2
Personalized and predictive medicine for pediatric diabetes through a genetic test using next generation sequencing.
Geneva, Switzerland
Thu 27 16:10
RFC3.3
Significant prevalence of severe monogenic immune defects among children with Type 1 diabetes and low T1D-genetic risk score.
Prague, Czech Republic
Thu 27 16:20
RFC3.5
Recent secular change in pre- and postnatal growth and adiposity in Infants of Mothers with Gestational Diabetes.
Cambridge, UK
Thu 27 16:00
RFC4.1
Metabolomic changes in patients with PAPP-A2 deficiency in response to rhIGF1 treatment.
Madrid, Spain
Thu 27 16:10
RFC4.3
A deletion encompassing exon 2 of the alsgene: Analysis of a patient with ALS deficiency and his family.
Santiago, Chile
Thu 27 16:20
RFC4.5
12-Month effects of once-weekly and twice-monthly administration of hybrid Fc-fused human growth hormone, GX-H9, treatment in pediatric with GHD deficiency.
Seoul, Republic of Korea
Thu 27 16:25
RFC4.6
Effect of 2 years of Growth Hormone Treatment on Glucose Tolerance in Adults with Prader-Willi Syndrome.
Rotterdam, The Netherlands
Thu 27 16:15
RFC5.4
The value of cytological, histological and US examination to determine of management children with nodular goiter.
Moscow, Russian Federation
Thu 27 16:20
RFC5.5
Evidence for a founder effect in Multiple Endocrine Neoplasia 2.
Nicosia, Cyprus
Thu 27 16:25
RFC5.6
DUOX2 Deficiency in Quebec: From Life-threatening Compressive Goiter in Infancy to Lifelong Euthyroidism.
Montréal, Canada
Fri 28 09:40
FC6.2
Fri 28 09:50
FC6.3
Fri 28 10:10
FC6.5
Fri 28 10:00
FC7.4
Altered substrate specificities and metabolite production by aromatase (CYP19A1) due to the R192H mutation.
Bern, Switzerland
Fri 28 10:10
FC7.5
Thyroid hormone levels in cord blood are associated with fetal and neonatal growth.
Copenhagen, Denmark
Fri 28 09:30
FC8.1
Estrogen Receptor 2 Variant as a Novel Cause for Dysgenetic Ovaries.
Fribourg, Switzerland
Fri 28 09:40
FC8.2
Partial restoration of biological effects of estrogen in a female with estrogen receptor α variant.
Nancy, France
Fri 28 10:00
FC8.4
STARD8, a novel candidate gene for 46,XY disorders of sex development.
Fribourg, Switzerland
Fri 28 10:10
FC8.5
DEAH-box helicase 37defects (DXH37) deffects are a Novel Cause of 46,XY Gonadal Dysgenesis.
Sao Paulo, Brazil
Fri 28 10:20
FC8.6
The roles of steroids in gonadal development and maintenance – insights from a zebrafish model of androgen and cortisol deficiency.
Sheffield, United Kingdom
Fri 28 09:50
FC9.3
Mutations in MAGEL2 and L1CAM are associated with congenital hypopituitarism and arthrogryposis.
London, UK
Fri 28 09:50
FC10.3
Fri 28 10:20
FC10.6
Primary ovarian insufficiency incidence rate and etiology among Israeli adolescents between the years 2000-2016 – A multi-center study
Ramat Gan, Israel
Fri 28 10:30
RFC6.1
Allelic variation in key fitness genes is linked with increased severity of obesity in overweight/obese youth.
Parkville, Australia
Fri 28 10:35
RFC6.2
IGF-I at four months associates to visceral and subcutaneous adipose tissue at 7 years of age.
Gothenburg, Sweden
Fri 28 10:45
RFC6.4
Functionality and phenotypic characteristics of mutations in the human leptin receptor.
Ulm, Germany
Fri 28 10:55
RFC6.6
Fri 28 10:30
RFC7.1
Next generation sequencing results in 142 patients with congenital hyperinsulinism.
Moscow, Russian Federation
Fri 28 10:35
RFC7.2
Outcomes of a quality improvement project integrating Continuous Glucose Monitoring Systems into the routine management of neonatal hypoglycaemia.
London, United Kingdom
Fri 28 10:40
RFC7.3
Central venous cathether-associated thrombosis in children with congenital hyperinsulinism.
Manchester, UK
Fri 28 10:55
RFC7.6
Assessment of Pituitary Stalk Anatomy by T2 DRIVE without Gadolinium in Pituitary Diseases.
Genoa, Italy
Fri 28 10:55
RFC8.6
Metabolic profile of young adult transgender persons who started gender affirming treatment in their adolescence.
Amsterdam, The Netherlands
Fri 28 10:30
RFC9.1
Clinical and genetic features of central precocious puberty associated with complex phenotypes.
São Paulo, Brazil
Fri 28 10:35
RFC9.2
Novel variant in GNRHR gene regulatory region in a pedigree with maternally inherited precocious puberty.
Ljubljana, Slovenia
Fri 28 10:50
RFC9.5
Non-isolated central precocious puberty: prevalence of brain lesions and other associated disorders.
Paris, France
Fri 28 10:55
RFC9.6
Can neuroimagine predict endocrine morbidity in congenital hypothalamo-pituitary (H-P) disorders?
London, UK
Sat 29 09:10
FC11.2
Sat 29 09:30
FC11.4
Using patient derived induced pluripotent stem cells to model multiple epiphyseal dysplasia.
Manchester, UK
Sat 29 09:40
FC11.5
A recurrent 6-bp intronic deletion in NESP55 with reduced penetrance in pseudohypoparathyroidism type 1b.
Philadelphia, USA
Sat 29 09:10
FC12.2
Apoptosis and oxidative stress markers during the Oral Glucose Tolerance Test (OGTT).
Sparta, Greece
Sat 29 09:30
FC12.4
How does thiol/disulphide homeostasis change in children with type 1 diabetesmellitus?
Ankara, Turkey
Sat 29 09:40
FC12.5
Effect of Homocysteine-Lowering Therapy on Diabetic Nephropathy in Children and Adolescents with Type 1 Diabetes.
Cairo, Egypt
Sat 29 09:50
FC12.6
Persistent beneficial effects of metformin in children and adolescents with type 1 diabetes: Adelaide metformin randomized controlled trial follow up.
North Adelaide, Australia
Sat 29 09:00
FC13.1
Sat 29 09:10
FC13.2
Sat 29 09:20
FC13.3
Sat 29 09:40
FC13.5
Study of the serum kisspeptin level in healthy and hypogonadotropic boys.
Saint-Petersburg, Russian Federation
Sat 29 09:50
FC13.6
Teamwork saves lives: how pediatric multidisciplinary care can prevent ‘unexplained deaths’ in adults with Prader-Willi syndrome.
Rotterdam, The Netherlands
Sat 29 09:30
FC14.4
Glucocorticoid deficiency causes differentially dysregulated oxidative stress depending on the steroidogenic defects.
Sheffield, UK
Sat 29 09:00
FC15.1
The diagnostic yield of a targeted next generation sequencing panel in children with short stature of undefined aetiology.
Manchester, UK
Sat 29 09:30
FC15.4
Sat 29 09:40
FC15.5
Utility of BDNF and MMP-1 as markers of cardiometabolic risk in Turner syndrome girls.
Katowice, Poland
Sat 29 09:50
FC15.6
Sat 29 10:00
RFC11.1
Diagnosis and management of pseudohypoparathyroidism and related disorders: First international consensus statement.
Lübeck, Germany
Sat 29 10:05
RFC11.2
Sat 29 10:10
RFC11.3
Increased levels of bone formation and resorption markers in patients with hypophosphatemic rickets.
Kolding, Denmark
Sat 29 10:15
RFC11.4
A new form of Anhidrotic Ectodermal Dysplasia with Immunodeficiency caused by abolished Store-Operated Ca2+ Entry.
Zagreb, Croatia
Sat 29 10:20
RFC11.5
Sat 29 10:25
RFC11.6
Reference Values of Automated Bone Age and Bone Health Index for Mexican children and adolescents.
Mexico City, Mexico
Sat 29 10:00
RFC12.1
Use of acid-suppressive medications during infancy and early childhood and its association with type 1 diabetes.
Cleveland, USA
Sat 29 10:05
RFC12.2
Bone mineral density is increased in 276 Danish children and adolescents with Type-1-Diabetes.
Herlev, Denmark
Sat 29 10:10
RFC12.3
Barriers and sources of support for the performance of physical activity inpediatric type 1 diabetes.
Haifa, Israel
Sat 29 10:15
RFC12.4
Use of telemonitoring via a mobile device app reduces HbA1c in type 1 diabetic children and adolescents.
Geneva, Switzerland
Sat 29 10:20
RFC12.5
Insulin gene promoter methylation status in Greek children and adolescents with Type 1 Diabetes.
Thessaloniki, Greece
Sat 29 10:25
RFC12.6
AMGLIDIA, a suspension of glibenclamide for patients with neonatal diabetes, long term data on efficiency and tolerance.
Paris, France)
Sat 29 10:10
RFC13.3
Circulating MKRN3, Kisspeptin and IGF-1 levels in girls during the clinical onset of puberty.
Chengdu, China
Sat 29 10:15
RFC13.4
Sat 29 10:20
RFC13.5
Pubertal voice break: Temporal relation of secondary sexual characteristics in healthy boys.
Copenhagen, Denmark
Sat 29 10:25
RFC13.6
Close correlation between salivary and blood steroids in normal boys: Salivary testosterone best characterizes male puberty.
Freiburg, Germany
Sat 29 10:00
RFC14.1
Psychometric and Psycho-social Profile of Children and Adolescent Survivors of Pediatric Cancer.
Athens, Greece
Sat 29 10:10
RFC14.3
Dysregulated glucose homeostasis in Congenital Central Hypoventilation Syndrome.
South Brisbane, Australia
Sat 29 10:15
RFC14.4
A novel germline DICER1 mutation in a girl with multinodular goiter and ovarian Sertoli-Leydig cell tumor.
Bethesda, USA
Sat 29 10:20
RFC14.5
Natural course of MEN type 2B syndrome; a Dutch single-center cohort.
Utrecht, The Netherlands
Sat 29 10:25
RFC14.6
Identification of epithelial sodium channel (ENaC) in endometrial pipelle biopsy samples.
Holon, Israel
Sat 29 10:20
RFC15.5
Effect of Adjusting for Tanner Stage Age on Short and Tall Stature Prevalence in US Youths.
Minneapolis, USA
Thu 27 17:15
MTE4.1
Fri 28 08:30
MTE8.1
Sat 29
MTE4.2
Sat 29 14:00
MTE8.2
Fri 28 08:00
PL3
Fri 28 12:00
PL4
Fri 28
PL5
Dynamic control of tissue glucocorticoids – lessons for optimising replacement therapy
Edinburgh, UK
Sat 29 17:30
PL8
Fri 28
YB2.1
Fri 28
YB2.5
Sat 29 09:20
HDI2.2
...Manage a child with physical disabilities who has a low bone mineral density
Melbourne, Australia
Sat 29 09:40
HDI2.3
Sat 29
YI1.1
Sat 29
YI1.2
Adipokines and genetic markers of childhood obesity and insulin resistance
Bratislava, Slovakia
Thu 27 12:00
SS1.1
Thu 27 12:30
SS1.2
Fascinating growth phenomena: what causes individual catch-up growth and population secular change
Leiden, The Netherlands
Thu 27 13:00
SS1.3
Interaction between nutrition, the endocrine system and the growth plate
Petah Tikva, Israel
Thu 27 12:00
S1.1
The molecular basis of Combined Pituitary Hormone Deficiency: lessons from animal models
Michigan, USA
Thu 27 12:00
S2.1
The biology of germ cell tumors in Disorders of Sex Development
Rotterdam, The Netherlands
Thu 27 15:20
HDI1.2
…Differentiate between constitutional delay in growth and puberty and hypog hypog?
Tubingen, Germany
Thu 27 15:40
HDI1.3
Fri 28
S4.2
Fri 28
S4.3
Fri 28
S5.1
Fri 28
S6.1
The biology of the glucocorticoid receptor: new signaling mechanisms in health and disease
North Carolina, USA
Fri 28
NA1.2
Sat 29 15:30
S7.1
Sat 29 16:30
S8.3
Paediatric differentiated thyroid cancer: outcome and long term effects
Groningen, The Netherlands
Sat 29 15:30
S10.1
Sat 29 16:30
S10.3
Sat 29
AC1.1
The ESPE roadmap to a career in academic paediatric endocrinology
Glasgow, United Kingdom
Sat 29
AC1.2
Sat 29
AC1.4
0 result(s) found.