EUROPEAN SOCIETY FOR PAEDIATRIC ENDOCRINOLOGY

59th Annual ESPE Meeting

 

22-26 September 2021 Virtual Conference
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N. Poster
Poster title
Applicant name
Status
  P2-001 Circadian rhythm of salivary cortisol and cortisone in school-aged children born very preterm and adequate for gestational age Gonzalo Dominguez-Menendez Received Received
  P1-001 Optimizing the timing of highest hydrocortisone dose in children and adolescents with 21-hydroxylase deficiency Mariska Schrder Received Received
  P1-002 Adrenocortical hormone profiles do not predict the molecular etiology in non-CAH primary adrenal insufficiency Tuba Seven Menevse Received Received
  P2-002 How do urine steroid metabolites of spot samples correlate with 24 hour urine specimens in children with congenital adrenal hyperplasia? Grit Sommer Received Received
  P1-003 Growth-Related Characteristics of Patients 18 Years of Age with Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency (21OHD): Real-World Evidence from the I-CAH Registry Mallory Farrar Received Received
  P2-003 Endocrine-disrupting chemicals: an often-forgotten etiology of endocrinological disturbances Júlia Galhardo Received Received
  P2-004 SERUM SEX HORMONE BINDING GLOBULIN LEVELS, BUT NOT 4-HOUR PROFILE OF 17-OH PROGESTERONE, WOULD BE USEFUL IN MONITORING CHILDREN WITH CONGENITAL ADRENAL HYPERPLASIA Ozge Besci Received Received
  P1-004 Depression among insured children and young adults in the United States with congenital adrenal hyperplasia Lauren Harasymiw Received Received
  P2-005 Glucocorticoid side-effects in Duchenne Muscular Dystrophy: Systematic review of side effects in published literature and a survey of the concerns of the patient community Caleb Hariri Received Received
  P1-005 Alterations in resting-state functional connectivity in patients with congenital adrenal hyperplasia Valeria Messina Received Received
  P2-006 Single centre experience of Hydrocortisone Granules (Alkindi) in children under 6 years of age with Adrenal Insufficiency Claire Snow Received Received
  P1-006 International practice of therapy monitoring in congenital adrenal hyperplasia Real World data from the I-CAH registry Neil Lawrence Received Received
  P2-007 Emotion regulation in congenital adrenal hyperplasia Annelies vant Westeinde Received Received
  P1-007 Brain activity during working memory in congenital adrenal hyperplasia Annelies vant Westeinde Received Received
  P2-008 High-dose steroids in the management of Paediatric Multisystem Inflammatory Syndrome Temporally associated with SARS-CoV-2 (PIMS-TS): Considering the hypothalamic-pituitary-adrenal axis Sinead McGlacken-Byrne Received Received
  P1-008 Long-term Cardiometabolic Morbidity In Young Adults With Classic 21-Hydroxylase Deficiency Congenital Adrenal Hyperplasia Beatrice Righi Received Received
  P1-009 Backdoor Pathway hormones and 11-oxygenated Androgens are elevated in Patients with 21-hydroxylase deficiency Alexandra Kulle Received Received
  P2-009 Variability of advice and education for steroid sick day dosing in Duchenne Muscular Dystrophy and the impact of the COVID-19 pandemic: Results of a UK wide patient survey Sze Choong Wong Received Received
  P1-010 Glucose regulation in children with primary adrenal insufficiency: preliminary data. Julie Park Received Received
  P2-010 Clinical characteristics of cytochrome P450 oxidoreductase deficiency: a nationwide survey in Japan Shuichi Yatsuga Received Received
  P2-011 Rare Presentation of Adrenal Insufficiency in an Infant with Holocarboxylase Synthetase Deficiency Aws Al-Farsi Received Received
  P1-011 Bone and endocrine monitoring in boys with Duchenne Muscular Dystrophy Sze Choong Wong Received Received
  P1-012 Real-world clinical profiles of children with hypophosphatasia (HPP) from the Global HPP Registry Gabriel Martos-Moreno Received Received
  P2-012 Defective Cortisol Secretion in Response to Spontaneous Hypoglycemia but Normal Cortisol Response to ACTH stimulation in neonates with Hyperinsulinemic Hypoglycemia (HH). Shayma Ahmed Received Received
  P1-013 Characterisation and phenotype-genotype associations of a large cohort of patients with pseudohypoparathyroidism type 1A and 1B Philippa Prentice Received Received
  P2-013 Utilisation Of The I-CAH Registry As A Tool For Facilitating Health Quality Improvement Strategies- Results Of An International Survey Of Specialist Centres Salma Ali Received Received
  P1-014 Tumor induced osteomalacia, a rare and complex condition with more treatment options, exemplified in two patients. Niels Birkebk Received Received
  P2-014 Clinical and hormonal evolution of aldosterone synthase deficiency: Is complete remission possible? Busra Gurpinar Tosun Received Received
  P2-015 Clinical and metabolic characteristics of hyperandrogenic girls with non-classic congenital adrenal hyperplasia and polycystic ovary syndrome Teodora Karamfilova Received Received
  P1-015 Vitamin D status and recommendations in Paediatric Inflammatory Multisystem Syndrome Temporarily associated with SARS-CoV-2 (PIMS-TS) James Robert Brighouse Received Received
  P2-016 Rapid clearance of hydrocortisone as a cause of poor control of CAH detected by 24-hour profiling of hydrocortisone concentrations. Aikaterini Iordanidou Received Received
  P1-016 Leptin to adiponectin ratio at the age of 12 is negatively associated with lumbar spine bone mineral apparent density independently of body fat mass in 18-year old males. Vallo Tillmann Received Received
  P2-017 A PROSPECTIVE STUDY OF CHILDREN 0-8 YEARS WITH CONGENITAL ADRENAL HYPERPLASIA AND ADRENAL INSUFFICIENCY ON TREATMENT WITH HYDROCORTISONE GRANULES MONITORED BY 17-OHP SALIVA SAMPLING Uta Neumann Received Received
  P1-017 Clinical Spectrum of Hypomagnesemia type 1 (HOMG1) due to Novel TRPM6 mutations Sommayya Aftab Received Received
  P1-018 A rare cause of hypercalcemia: Congenital Lactase Deficiency Mehmet Eltan Received Received
  P2-018 Cushings disease treatment results correlation with pituitary MRI in children Eda Yanar Received Received
  P1-019 Acetazolamide treatment in a patient with pseudohypoparathyroidism with venous calcification Tuba Seven Menevse Received Received
  P2-019 Genetic analysis of paediatric primary adrenal insufficiency of unknown aetiology over 25 years federica buonocore Received Received
  P2-020 Panhypopituitarism after treatment procedures in pituitary-hypothalamic area a single center experience Yuliya Bazdarska Received Received
  P1-020 A novel TRPM6 variant (c.3179TA) causing familial hypomagnesemia with secondary hypocalcemia Meghna Chawla Received Received
  P2-021 The reliability of Salivary Cortisol compared to Serum Cortisol for diagnosing adrenal insufficiency in the gold standard ACTH stimulation test in children Silvia Ciancia Received Received
  P1-021 Incidence of Type 1 Diabetes in Children and Adolescents during the Covid-19 Pandemic in Germany: Results from the DPV registry Clemens Kamrath Received Received
  P2-022 Prevalence of adrenal insufficiency (AI) requiring treatment with hydrocortisone in children tested with the LDSST Julie Park Received Received
  P1-023 Capillary blood sample collection at home for HbA1c measurements during the COVID-19 pandemic in children with diabetes mellitus Rachel Qian Hui Lim Received Received
  P2-023 Serum cortisol and cortisone, and urinary cortisol, cortisone, and tetrahydro-metabolites concentrations in school-aged children born very preterm adequate for gestational age Gonzalo Dominguez-Menendez Received Received
  P1-024 Resolution of feeding problems in patients with congenital hyperinsulinism Chris Worth Received Received
  P2-024 The incidence and presentation of congenital adrenal hyperplasia in an unscreened population Tracey Anne Conlon Received Received
  P1-025 Longitudinal Auxological Recovery and Reduced Neurodevelopmental Problems in Hyperinsulinaemic Hypoglycaemia Chris Worth Received Received
  P2-025 Genotypic Sex and Severity of the Disease Determine the Time of Clinical Presentation in Steroid 17a-Hydroxylase/17,20-Lyase Deficiency Erdal Kurnaz Received Received
  P1-026 Efficacy and Tolerability of GLP-1 Receptor Agonists in Children and Adolescents with Obesity Paul MacDaragh Ryan Received Received
  P2-026 Testicular adrenal rest tumour in children with classical congenital adrenal hyperplasia: A case series. Hooi Peng Cheng Received Received
  P1-027 The SARS-CoV-2 Pandemic Is Associated With Increased Severity Of Presentation Of Childhood Onset Type 1 Diabetes Mellitus: A Multicentre Study Of The First COVID-19 Wave Sinead McGlacken-Byrne Received Received
  P2-027 High doses op-DDD cause metrorragia in young girls Cecile Thomas-Teinturier Received Received
  P2-028 An Adolescent Case With Adrenoleukodystrophy Diagnosed After Detection Of Leydig Cell Dysfunction Iclal Okur Received Received
  P1-029 Incidence and severity of new-onset paediatric Type 1 diabetes in the COVID-19 pandemic a UK multicentre perspective Sophia Sakka Received Received
  P2-029 FLUDROCORTISONE IS THE SALVAGE TREATMENT IN CASES WITH CALCINEURIN INHIBITOR RELATED HYPERKALEMIA Yagmur Unsal Received Received
  P2-030 Development of a novel weight-based steroid emergency plan for patients with Duchenne Muscular Dystrophy Sally Tollerfield Received Received
  P1-030 Metabolic Control and Health-Related Quality of Life in Children with Diabetes Mellitus during the COVID-19 Pandemic: Results from a Prospective Swiss Cohort Study Serpil Vural Received Received
  P1-031 Efficacy and Safety of Setmelanotide in Individuals With Obesity Due to POMC or LEPR Deficiency: Phase 3 Results From Pivotal and Supplemental Cohorts Kristi ODonovan Received Received
  P2-031 Investigation of usage and acceptance of hydrocortisone granules in capsules for opening in children with adrenal insufficiency Uta Neumann Received Received
  P2-032 Congenital Adrenal Hyperplasia caused by homozygous pathogenic variant in the HSD3B2 gene. Eirini Fylaktou Received Received
  P1-032 Sex hormones drive changes in lipoprotein profiles in adolescents; early implications for cardiovascular disease risk George Robinson Received Received
  P1-033 Metabolomics in early life and the association with body composition at age 2 years Inge van Beijsterveldt Received Received
  P2-033 Congenital Adrenal Hyperplasia with a CYP21A2 deletion overlapping Tenascin-X gene Catarina Rodrigues Ivo Received Received
  P2-034 Maternal primary adrenal cortex insufficiency during pregnancy: Spotlight on the Fetus and the Neonate. A systematic review and meta-analysis. Georgia Ilia Received Received
  P1-035 The possible association of the apoptotic marker APO1/Fas with predisposition to metabolic syndrome and mean platelet volume in children Eirini Kostopoulou Received Received
  P2-035 Assessment of blood pressure and carotid intima media thickness (CIMT) in children with primary adrenal insufficiency Julie Park Received Received
  P1-036 Reversal of metabolic derangement in patient with congenital generalized lipodystrophy treated with metreleptin Jamal Aljubeh Received Received
  P2-036 Challenges in diagnosis and treatment of Cushing Disease in a 12 years old boy Agim Gjikopulli Received Received
  P1-037 The effect of trans-palmitoleic acid on lipid accumulation and the fatty acid synthase gene expression in hepatocytes Mitra Nourbakhsh Received Received
  P2-037 Congenital Adrenal Hyperplasia caused by compound heterozygosity of two novel CYP11B1 gene variants. Eirini Fylaktou Received Received
  P1-038 Are Serum Spexin Levels Associated With Metabolic Syndrome Antecedents In Obese Adolescents? Ahmet Uar Received Received
  P2-038 Addisons disease: Delay in diagnosis in a girl with longstanding symptoms Myrto Bonataki Received Received
  P2-039 Clinical spectrum of congenital adrenal hyperplasia due to 3 beta hydroxysteroid dehydrogenase deficiency ;A case series Tahir Shaheen Received Received
  P1-039 Serum endocan as a predictive biomarker of cardiovascular risk in obese pediatric patients Selenia Curatola Received Received
  P1-040 Liraglutide for the Management of Childhood Obesity Louise Apperley Received Received
  P2-040 Retrospective Evaluation of Cases Diagnosed with Classical Congenital Adrenal Hyperplasia Due to 21 Hydroxylase Deficiency elmaogullari Selin Received Received
  P2-041 CORTICOTROPIN-INDEPENDENT CUSHING SYNDROME IN TODDLERHOOD: A CHALLENGING DIAGNOSIS AND TREATMENT Julia Galhardo Received Received
  P1-041 Phenotypic Characteristics of Patients with 45,X/46,XY Mosaicism: Growth, Gonadal Pathology and Tumour Risk Sukran Poyrazoglu Received Received
  P2-042 A case of adrenal insufficiency during the course of multisystem inflammatory syndrome in children (MIS-C) Fatih Kilci Received Received
  P1-042 Disorders of sex development: clinical and genetic heterogeneity Irina Nikitina Received Received
  P2-043 Aetiology and different clinical conditions of primary adrenal insuffiency in a region of North Africa Fadila Bouferoua Received Received
  P1-043 Broad range of phenotypes in an international cohort of 75 DSD individuals with SF-1/NR5A1 variants Chrysanthi Kouri Received Received
  P1-044 Adolescents and young adult men with non-syndromic hypospadias: testicular function and in-depth genetic screening Lloyd Tack Received Received
  P2-044 Clinical and evolutionary aspects of Allgrove Syndrome, Algerian experience Bouferoua Fadila Received Received
  P1-045 Bilateral testicular regression: etiology and outcome in a large Belgian series Lloyd Tack Received Received
  P2-045 A Rare Coexistence of two autosomal recessive conditions: Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency (CYP21A2 mutation) with Beta Thalassemia Major Aniqa Aslam Received Received
  P1-046 Endocrine & Molecular Genetic Findings In XY Boys Investigated For A Disorder Of Sex Development: The Glasgow Experience Malika Alimussina Received Received
  P2-046 X- linked Adrenoleukodystrophy in southern of Tunisia Sana Kmiha Received Received
  P2-047 Clinical, biological and genetic aspects of congenital adrenal hyperplasia in children at the Central Hospital of Army in Algiers Malek Iabbassen Received Received
  P1-047 STK11 gene variant (Peutz-Jeghers Syndrome) presenting with unilateral pre-pubertal gynaecomastia and macro-orchidism without muco-cutaneous pigmentation or gastrointestinal symptoms. Meera Shaunak Received Received
  P2-048 Coexistence of Adrenal Insufficiency and Hypergonadotropic Hypogonadism: P450scc Deficiency Merve Sakar Received Received
  P1-048 Gonadal Outcome in 17beta-HSD deficiency and 5alpha-reductase deficiency Lidewij S Boogers Received Received
  P2-049 Assessment of Patients With Congenital Adrenal Hyperplasia in Armenia Renata Markosyan Received Received
  P1-049 Biallelic PPP2R3C mutations are associated with partial and complete gonadal dysgenesis in 46,XY and 46,XX individuals Tulay Guran Received Received
  P1-050 Pathogenic variants in the human m6A reader YTHDC2 are associated with primary ovarian insufficiency Sinead McGlacken-Byrne Received Received
  P2-050 First case in Lebanon of homozygous mutation in CYP 11B2 leading to isolated aldosterone deficiency. Ahlam Azar Received Received
  P2-051 A Rare Cause of Hyponatremia in a Child with Hirschsprung Disease Operated with an Ileostomy Abeer Alassaf Received Received
  P1-051 A Global Natural History Study (NHS) of Fibrodysplasia Ossificans Progressiva (FOP): Normal Long Bone Growth and Abnormalities in Younger Patients over 36 Months Will Cherry Received Received
  P1-052 Impact of Vertebral Fracture on Auxological Profile and Insulin-like Growth Factors of Children after Acute Lymphoblastic Leukemia Treatment Moon Bae Ahn Received Received
  P1-053 Growth and Puberty in Patients with Osteogenesis Imperfecta Ay&351;e p&305;nar ztrk Received Received
  P2-053 Mutation of NROB1 and Double mutants in cis of CYP21A2 gene in a Chinese boy with primary adrenal insufficiency Huamei Ma Received Received
  P1-054 Decreased bone mineral density in children receiving long-term anticoagulation is associated with pubertal development Adalbert Raimann Received Received
  P2-055 Twin infants with salt-wasting: double the trouble Ana Graneiro Received Received
  P1-055 Premature epiphyseal fusion induced by a retinoic acid agonist in a young girl with fibrodysplasia ossificans progressiva Sigrún Hallgrímsdóttir Received Received
  P2-056 Effect of treatment of double precocious puberty in a 9-year-old girl- case report Beata Sawicka Received Received
  P1-056 Chondrocyte regulating and other growth plate genes are invaluable growth regulators: a study on children with short stature from 55 consanguineous families Shenali Anne Amaratunga Received Received
  P1-057 High rate of positive genetic findings in children born small for gestational age with persistent short stature (SGA-SS): Growth plate genes as key regulators of intrauterine growth Ledjona Toni Received Received
  P2-057 Classical Congenital adrenal hyperplasia: about 7 cases najat draoui Received Received
  P1-058 AAV liver gene therapy-mediated inhibition of FGF23 signaling as a therapeutic strategy for X-linked hypophosphatemia Volha Zhukouskaya Received Received
  P2-058 Denosumab therapy for giant cell granuloma in a paediatric patient: using quantification of Tc99m-MDP uptake on SPECT imaging to guide treatment. Laura Wade Received Received
  P2-059 Vertebral compression and shape in children with osteogenesis imperfecta on regular Zoledronic acid infusions Alaa Baioumi Received Received
  P1-059 Cartilage -specific knockout of SIRT1 significantly reduces bone quality and catch-up growth efficiency Galia Gat-Yablonski Received Received
  P2-060 Osteosclerotic Metaphyseal Dysplasia: A novel homozygous LRRK1 mutation in two siblings Chariklia Pieridou Received Received
  P1-060 Mosaic PHEX variants are important causes of X-linked hypophosphataemic rickets. Philippa Prentice Received Received
  P2-061 Experience of 6-months of burosumab therapy in five siblings with X-linked hypophosphataemic rickets in the State of Kuwait Sameer Al Shammari Received Received
  P1-061 Clustering of Hypoglycaemia Events in Patients with Hyperinsulinism (HI): Extension of the Digital Phenotype Chris Worth Received Received
  P1-062 Epidemiology of type 1 diabetes in children and adolescents: a 50-year, single center experience Dogus Vuralli Karaoglan Received Received
  P2-062 Severe Hypophosphatemic Rickets due to Tumor-Induced Osteomalasia Belma Haliloglu Received Received
  P1-063 Comparison of triglyceride and glucose index and homeostatic model assessment for insulin resistance in children and adolescents with type 2 diabetes mellitus Jong Seo Yoon Received Received
  P2-063 Diagnostic Challenges of Vitamin D-Dependent Rickets Type 1A (VDDR1A) caused by CYP27B1 mutation in Resource Limited Countries: A Case Series from Three families Sommayya Aftab Received Received
  P2-064 Lack of Cinacalcet response in Neonatal Severe Hyperparathyroidism (NSHPT) due to homozygous CASR mutation Ammar Haider Received Received
  P1-064 Initial Neutrophil/Lymphocyte and Lymphocyte/Monocyte Ratios Can Predict Future Insulin Need in Newly Diagnosed Type 1 Diabetes Mellitus Ibrahim Mert Erbas Received Received
  P1-065 Efficacy of use of Continuous Glucose Monitoring System in patients with Congenital Hyperinsulinism Yesica Tropeano Received Received
  P2-065 Is conventional treatment still the first choice in pediatric patients with PHEX mutations in an era of monoclonal FGF-23 antibody? Yagmur Unsal Received Received
  P1-066 Mortality in children with monogenic diabetes Eugenia Globa Received Received
  P2-066 Vosoritide Clinical Study Data Demonstrates CXM is a Superior Biomarker of Endochondral Bone Growth Kevin Larimore Received Received
  P1-067 The Molecular Genetic Etiology by Whole Exome Sequence Analysis in Cases With Familial Type 1 Diabetes Mellitus without HLA Haplotype Predisposition or Incomplete Predisposition ferda evin Received Received
  P1-068 Birth weight and diazoxide unresponsiveness strongly predict the likelihood of congenital hyperinsulinism due to a mutation in ABCC8 or KCNJ11 Thomas Hewat Received Received
  P1-069 Oxidized lipid-associated protein damage in children and adolescents with type 1 diabetes mellitus: new diagnostic/prognostic clinical markers. Eirini Kostopoulou Received Received
  P2-069 Evaluation of Admission Characteristics, Treatment and Follow-up Findings of Children with Primary Osteoporosis Sirmen Kizilcan Cetin Received Received
  P1-070 Change in HbA1C predicts future abnormal Oral Glucose Tolerance Tests in children and adolescents with Cystic Fibrosis. Sommayya Aftab Received Received
  P2-070 Phenotype characterization of a PHEX intron mutation in an Italian family affected by X linked hypoposphatemic rickets. Francesca Aiello Received Received
  P1-071 Morning salivary cortisol and stress response in term and preterm infants hospitalized in the intensive care unit. Marta Olszewska Received Received
  P1-072 Clinical characteristics of children with Congenital Hyperinsulinism: Results from the European Registries for Rare Endocrine Conditions (EuRRECa) Project Lukas Plachy Received Received
  P2-072 ACAN GENE SKELETAL DYSPLASIA (SHORT SIZE SYNDROME, WITH OR WITHOUT ADVANCED BONE AGE AND EARLY ONSET OSTEOARTHRITIS) Cristina Aguilar Riera Received Received
  P1-073 MINIPUBERTY IN BORN SMALL FOR GESTATIONAL AGE INFANTS: A CASE CONTROL PROSPECTIVE PILOT STUDY Giorgia Pepe Received Received
  P2-073 PTEN downregulation in mouse osteoprogenitor cells impacts on bone stability and turnover Judith Lorenz Received Received
  P1-074 Pancreatic glucagon-like-peptide-1 receptor expression in congenital hyperinsulinism Diliara Gubaeva Received Received
  P2-074 Primary hyperparathyroidism due to a deletion of the CDC73 gene. Liliana Mejia de Beldjenna Received Received
  P2-075 AFEBRILE SEIZURE IN A TODDLER GIRL WITH ALOPECIA: A CASE REPORT Julia Galhardo Received Received
  P1-075 Congenital hyperinsulinism diagnosed after 12 months can have a monogenic aetiology Jasmin Hopkins Received Received
  P1-076 Hyperinsulinemic Hypoglycemia in a child with Peroxisomal Biogenesis Disorder due to a Novel PEX1 mutation NIKHIL LOHIYA Received Received
  P2-076 A rare cause of hypophosphatemic rickets; Non-lethal Raine syndrome Glay Karagzel Received Received
  P2-077 Effect of tamoxifen on linear growth of precocious female SD rats Huamei Ma Received Received
  P1-077 Real-Time Continuous Glucose Monitoring in the Management of Neonates with Persistent Hypoglycemia Myat Win Received Received
  P2-078 Deleting STX16 exon 4 to understand the genetic mechanisms underlying pseudohypoparathyroidism-1B and GNAS imprinting Cagri Aksu Received Received
  P1-078 Hyperinsulinemic hypoglycemia due to biallelic mutations in the DNAJC3 gene Busra Gurpinar Tosun Received Received
  P1-079 Concurrent hyperinsulinism and hypopituitarism in a 22 month old child due to a novel FOXA2 mutation Fatih Kilci Received Received
  P2-079 Clinical, molecular characterization and long-term follow-up of a patient with neonatal severe hyperparathyroidism Ana Isabel Araújo Carvalho Received Received
  P1-080 Sphingosine 1- phosphate lyase insufficiency syndrome (SPLIS) as a cause of primary adrenal insufficiency and primary hypogonadism Ruth Kwong Received Received
  P2-080 Effect of Soy and Whey on growth pattern in young male Sprague-Dawley rats Meytal Bar Maisels Received Received
  P2-081 Early-onset osteoporosis due to LRP5 pilar acuña Received Received
  P1-081 Sporadic pituitary adenomas in young patients: clinical and molecular description Idoia Martinez de LaPiscina Received Received
  P1-082 Cardiac remodeling in patients with childhood-onset craniopharyngioma Results of HIT-Endo and KRANIOPHARYNGEOM 2000/2007 Panjarat Sowithayasakul Received Received
  P2-082 Vitamin D - What is the Optimal Level in the Pediatric Population David Gillis Received Received
  P1-083 Pregnancies after childhood craniopharyngioma Results of KRANIOPHARYNGEOM 2000/2007 Hermann L. Mller Received Received
  P1-084 Pituitary Duplication A rare and heterogenous spectrum Nicole Goff Received Received
  P2-084 A rare cause of childhood hypercalcemia: Parathyroid adenoma Havva Nur Peltek Kendirci Received Received
  P2-085 ONE GENE, TWO DISEASES:OSTEOGENESIS IMPERFECTA, OR BRUCK SYNDROME? hasan ar&305; Received Received
  P1-085 Auxological and endocrine aspects in pediatric patients with Narcolepsy Type 1. Results of long-term follow up in a Pediatric Endocrinology Center Valentina Assirelli Received Received
  P1-086 Adding a protease inhibitor to sampling tubes increases the acylated ghrelin and decreases the desacylated ghrelin levels in girls. Maria Rodanaki Received Received
  P2-086 Spontaneous Reshaping of Vertebral Fractures in an Adolescent with Osteogenesis Imperfecta Rodrigo Montero Lopez Received Received
  P1-087 GHSR protects the emergence of limited sex differences in anxiety-related behaviors in adult mice after long term THC administration during peri-adolescence Maria Consolata Miletta Received Received
  P2-087 A rare presentation of Dysplasia Epiphysealis Hemimelica combined with Familial Hypocalciuric Hypercalcemia Is this association possible? Arthur H.T. Toledo Received Received
  P1-088 Pituitary microadenoma in childhood is follow-up with diagnostic imaging necessary? Camilla Borghammar Received Received
  P2-088 Two sibling cases with heterozygous calcium sensing receptor (CaSR) gene mutation Erdal Kurnaz Received Received
  P2-089 Clinical Profile of Parathyroid Adenoma in Children and Adolescents: A single-center experience Sirmen Kizilcan Cetin Received Received
  P1-089 The Pituitary Tumour Module: Developing a Condition Specific Module within the European Registries for Rare Endocrine Conditions (EuRRECa) Ana Luisa Priego Zurita Received Received
  P2-090 Changing reality: rebirth of old diseases in new circumstances. Severe vitamin D deficiency presenting as hypocalcemic seizures in a healthy adolescent after prolonged COVID-19 lock-down. Larisa Naugolny Received Received
  P1-090 Craniopharyngiomas presenting as incidentalomas: results of KRANIOPHARYNGEOM 2007 Svenja Boekhoff Received Received
  P2-091 Two-year experience of burosumab therapy in pediatric XLH patients in Saudi Arabia Fahad AlJuraibah Received Received
  P1-091 The effect of preoperative calcitriol prophylaxis on post-thyroidectomy hypocalcaemia in children Nitash Zwaveling-Soonawala Received Received
  P1-092 Emotional Intelligence scores in children and adolescents with subclinical hypothyroidism - correlation with serum serotonin and thyroid stimulating hormone (TSH) concentrations. Eirini Kostopoulou Received Received
  P2-092 Pseudohypoparathyroidism with hypokalemia and hypomagnesemia: association or separate entity? Arliena Amin Received Received
  P1-093 LYMPHOCYTE POPULATION IN CHILDREN AND ADOLESCENTS AFFECTED BY GRAVES DISEASE. POTENTIAL PREDICTIVE TOOL OF DISEASE SEVERITY Gerdi Tuli Received Received
  P2-093 Characterization of Patients with Achondroplasia in a pediatric Clinic of Cali, Colombia.P2-93 Liliana Mejia de Beldjenna Received Received
  P1-094 Evaluation of children with intrathyroidal ectopic thymus Emine Aya Cimbek Received Received
  P2-094 A Rare Cause of Familial Hypomagnesemia: A Case with Trpm6 Mutation Merve Sakar Received Received
  P1-095 Prevalence and Characteristics of thyroid nodules in a pediatric population with congenital hypothyroidism anne sophie lambert Received Received
  P2-095 Effect of cholecalciferol treatment on serum FGF-23, vitamin D-binding globulin and a-klotho levels in children with vitamin D deficiency Zerrin Orbak Received Received
  P1-096 Thyroid storm and transient bulbar myopathy in a 22-month-old girl with Graves Disease Jessica Sandy Received Received
  P2-096 HDR Syndrome (Barakat Syndrome): Case Report Omneya Magdy Omar Received Received
  P2-097 Hungry Bone Syndrome associated to Rickets Catalina Jiménez Received Received
  P1-097 The association between serum Thyrotropin within the reference range and cardiometabolic risk in obese children Angelo Tropeano Received Received
  P1-098 Hypothyroid Screening in Children with Down Syndrome - A Service Evaluation Rachael Harley Received Received
  P2-098 BUR-CL207: An Open-label, Multicenter, Non-randomized Study to Assess the Safety, Tolerability, Pharmacokinetics and Efficacy of Burosumab in Pediatric Patients from Birth to Less than 1 Year of Age with XLH. Lucy Henderson Received Received
  P1-099 Early adiposity rebound in children with congenital hypothyroidism diagnosed by newborn screening Tommaso Aversa Received Received
  P2-099 Characterization and Risk Factors of Hyperglycaemia During Treatment Of Childhood Hematologic Malignancies Sophie Welsch Received Received
  P1-100 Serum fibroblast growth factor 21 (FGF-21) levels of children and adolescents with Hashimotos thyroiditis, before and after L-thyroxin medication Eleni P Kotanidou Received Received
  P2-100 The knowledge and Confidence in Management of Diabetic Ketoacidosis (DKA) among Iraqi Paediatric Residents: a Cross Sectional Study Hussain Alsaffar Received Received
  P1-101 The management of adrenal cell carcinoma in a single tertiary centre: 25 year experience Nicole Goff Received Received
  P2-101 Disturbances of glucose homeostasis in polytransfused beta-thalassemia patients Noumi Mustapha Received Received
  P2-102 Unmet need in technology for diabetes management in the Middle East, Africa and South East Asia Hussain Alsaffar Received Received
  P1-102 Correlation of 11-oxygenated C19 androgens with the clinical and biochemical characteristics in premature adrenarche Zehra Yavas Abali Received Received
  P2-103 Diabetes in a child with infantile-onset multisystem neurologic, endocrine and pancreatic disease (IMNEPD) Marianne Becker Received Received
  P1-103 Leukocyte telomere length in children with Congenital Adrenal Hyperplasia Ozair Abawi Received Received
  P1-104 Cortison-loop is an educational tool, which helps ensure the quality of care for children with adrenal insufficiency. Camilla Ernstsson Received Received
  P2-104 The clinical characteristics of hybrid diabetes (HD) in children and their response to treatment. Noor Hamed Received Received
  P2-105 Recurrent episodes of hypoglycemia in an infant with type 1 spinal muscular atrophy after gene therapy: Beta oxidation defect exaggerated by hepatic dysfunction. Nada Alaaraj Received Received
  P1-105 The genetic etiology of ACTH-dependent aldosterone hypersecretion in hypertensive patients without Primary Aldosteronism Niki Mourtzi Received Received
  P1-106 Plasma Proteomics in Healthy Subjects with Differences in Tissue Glucocorticoid Sensitivity Identifies a Novel Proteomic Signature Nicolas Nicolaides Received Received
  P2-106 Knowledge of the Final Year Medical Students Compared to Interns about the Diagnosis and management of Diabetes Mellitus Hussain Alsaffar Received Received
  P2-107 A paradoxical conundrum: diabetic ketoacidosis resulting in treatment-resistant hypokalemic alkalosis Hande Rakicioglu Received Received
  P1-107 Cortoic Acids: Renaissance of a Forgotten Class of Steroids Marcel Schauermann Received Received
  P2-108 Impact of the COVID19 pandemic on Paediatric Diabetes Services in Arab Countries Hussain Alsaffar Received Received
  P1-108 Circadian rhythm of cortisol in saliva in obese children with clinical signs of hypercortisolism María Gabriela Ballerini Received Received
  P1-109 PLASMA STEROID PANEL WITH LIQUID CHROMATOGRAPHY-MASS SPECTROMETRY (LC/MS-MS) METHOD: UTILIZATION IN DIFFERANTIAL DIAGNOSIS OF HYPERANDROGENISM Aysun Ata Received Received
  P2-109 Clinical Case of Cystic Fibrosis-like and APECED-like Syndrome due to Gain-of-Function Variant in STAT1 Vasilev Teodor Received Received
  P2-110 A quality improvement project of a Young Adult Diabetes (YAD) service at a UK specialist centre. Dhruti Hirani Received Received
  P1-110 Current Management Of Acute Adrenal Insufficiency Related Adverse Events In Children- Results Of An International Survey Of Specialist Centres Salma Ali Received Received
  P2-111 Prevalence of skin reactions among pediatrics patients with Type 1 Diabetes users of glucose sensors. Beatriz Corredor Andrés Received Received
  P1-111 Insulin resistance following childhood craniopharyngioma may influence neural response to food cues in food reward-related brain regions: a preliminary investigation. Elanor Hinton Received Received
  P1-112 Evaluation of the BigO behavioral indicators in overweight and obese children and adolescents Athanasia Tragomalou Received Received
  P2-112 A single-centre evaluation of remote video consultation for children and young people with diabetes Edward Andrews Received Received
  P1-113 Are you considering Idiopathic Intracranial Hypertension when evaluating a patient with obesity? Louise Apperley Received Received
  P2-113 Health Outcome Indicators in Children with Diabetes Mellitus during the SARS-CoV-2 Pandemic Nikita Gireesh Bhat Received Received
  P2-114 EVALUATION OF SERUM MYOSTATIN LEVELS IN PATIENTS WITH INSULIN DEPENDENT DIABETES MELLITUS Beray Selver Eklio&287;lu Received Received
  P1-114 EuRRECa Registry Genetic Obesity Survey Results Guftar Shaikh Received Received
  P1-115 Circulating C1q Complement/TNF-Related Protein (CTRP)-13 Levels in Obese Children and Its Relationship with Metabolic Disorders Ibrahim Mert Erbas Received Received
  P2-115 HbA1c and Glucose Management Indicator relationship: can HbA1c determination be avoided? Constanza Navarro Moreno Received Received
  P1-116 An Evidence-based Framework to Evaluate Melanocortin-4 Receptor (MC4R) Pathway Relevance for Obesity-associated Genes Bhavik Shah Received Received
  P2-116 Sex differences over two decades for glycaemic control, pump use and insulin dose in patients aged 10-20 years with type 1 diabetes Claudia Boettcher Received Received
  P2-117 Cardiovascular risk factors in adolescents with type 1 diabetes: Prevalence and gender differences Dogus Vuralli Karaoglan Received Received
  P1-117 Serum Fibroblast Growth Factor 23 and Klotho concentrations in children and adolescents with obesity. Sofia-Iliada Karampatsou Received Received
  P2-118 Bilateral severe proliferative retinopathy, macular oedema, and lack of macrocytosis in an adolescent male with thiamine-responsive megaloblastic anaemia Manju Chandwani Received Received
  P1-118 RARE HETEROZYGOUS VARIANTS IN GENES OF THE LEPTIN-MELANOCORTIN SATIETY PATHWAY CONTRIBUTE TO CHILDHOOD OBESITY Gabriel Á. Martos-Moreno Received Received
  P1-119 Diagnostic precision of the Tri-Ponderal Mass Index (kg/m3) to identify the metabolically unhealthy obesity phenotype in obese children and adolescents. Larry Arciniegas Received Received
  P2-119 First Survey About Pediatric Diabetes Services in Iraq Hussain Alsaffar Received Received
  P2-120 Effect of metabolic control on the presence of Nonalcoholic Fatty Liver Disease (NAFLD) in adolescents with type 2 Diabetes. Jose Antonio Orozco Morales Received Received
  P1-120 Monogenic obesity in children: focusing on SH2B1 deletion Eleni Giannopoulou Received Received
  P1-121 Higher rates of non-skeletal complications in achondroplasia compared to the general population: a UK matched cohort study using the CPRD database Melita Irving Pimenta Received Received
  P2-121 The effect of glycemic variability on DNA damage in pediatric patients with type 1 Diabetes Mellitus Ayca Altincik Received Received
  P1-122 Short stature in Protein Arginine Methyltransferase 7 (PRMT7) mutations: first evidences of growth response to rGH treatment Giulia Rodari Received Received
  P2-122 Parental insulin resistance is associated with unhealthy lifestyle behaviours independently of body mass index in children: The Feel4Diabetes study Esther Gonzalez-Gil Received Received
  P1-123 Growth and nutrition improvement with recombinant growth hormone in prepubertal patients with Silver-Russell syndrome Elose Giabicani Received Received
  P2-123 Use of the whole country insulin consumption data in Israel showed a reduced prevalence of type 1 diabetes in children aged 5 years during universal Rotavirus vaccination Zvi Laron Received Received
  P2-124 PSYCHOLOGICAL CHANGES IN YOUTH WITH DIABETES: COMPARISON BETWEEN PREADOLESCENTS AND ADOLESCENTS Roberta Longaretti Received Received
  P1-124 Management of endocrine aspects of Noonan syndrome across Europe: A subanalysis of a European clinical practice survey Thomas Edouard Received Received
  P2-125 Focal Congenital Hyperinsulinism in Infancy is Directly Linked to Increased Numbers of Islet Pancreatic Polypeptide Cells in Islets. Chris Worth Received Received
  P1-125 PROPEL2: a phase 2, open-label, dose-escalation and dose-expansion study of infigratinib in children with achondroplasia (ACH) Lee Miller Received Received
  P1-126 Identification and tissue-specific characterization of novel SHOX-regulated genes in zebrafish highlights SOX family members among other genes Gudrun A. Rappold Received Received
  P2-126 Oral administration of CRN04777, a nonpeptide ive SST5 receptor agonist, suppresses insulin secretion and rescues hypoglycemia in neonatal rat models of congenital hyperinsulinism Melissa Fowler Received Received
  P1-127 Evaluation of early puberty in boys and girls with Silver-Russell Syndrome: Discordance between testicular growth and pituitary-gonadal hormones in male cases Melek Yildiz Received Received
  P2-127 Thiamine-responsive megaloblastic anemia: a rare presentation of an uncommon disease Yasmine Abdelmeguid Received Received
  P1-128 Evaluation of Persistent Short Stature in Children Born Small for Gestational Age without Catch-up Growth Ayse Pinar ztrk Received Received
  P2-128 Daily Meal Size Variation Does Not Affect Glycemic Control In T1D Adolescent Patients Equipped With The Closed Loop DBLG1 System Paul Gimenez Received Received
  P2-129 Evaluation of continuous glucose monitoring for the diagnosis of Cystic Fibrosis Related Diabetes (CFRD): A prospective and longitudinal study Pamela Yesquen Received Received
  P1-129 Computer-aided facial analysis as a tool to identify patients with Silver-Russell syndrome and Prader-Willi syndrome Silvia Ciancia Received Received
  P2-130 BLOOD LIPID CONCENTRATIONS OF NEWBORNS AND THEIR MOTHERS WITH GESTATIONAL DIABETES Olga Gumeniuk Received Received
  P1-130 Study design and baseline characteristics of children enrolled in PROPEL: A prospective clinical assessment study in children with achondroplasia (ACH) Lee Miller Received Received
  P2-131 Comparison between hybrid diabetes (HD) and type 2 diabetes (T2DM) in children; Patients characteristics at diagnosis: a retrospective observational study. Noor Hamed Received Received
  P1-131 The impact of lockdown regulations caused by the COVID-19 pandemic on adherence to recombinant human growth hormone therapy: Evidence from real-world data Paula Van Dommelen Received Received
  P1-132 Use of growth hormone therapy in short patients born small for gestational age: data from real-life French clinical practice Régis Coutant Received Received
  P1-133 Efficacy and safety profile of recombinant insulin like growth factor 1 (rh IGF1) therapy: A long term follow up study at a single tertiary centre. Sommayya Aftab Received Received
  P1-134 Starting recombinant human growth hormone treatment at an early age improves adherence and catch-up growth in patients with growth disorders, and highlights the importance of the new guideline on referral of short children to paediatric care Paula Van Dommelen Received Received
  P2-134 DOES SARS-COV-2 OUTBREAK INCREASES DIABETIC KETOACIDOSIS IN NEW ONSET T1DM Arzu Jalilova Received Received
  P1-135 Long-term safety of growth hormone in adults and adolescents with growth hormone deficiency: An overview of the full-cohort in KIMS Gudmundur Johannsson Received Received
  P2-136 Evaluation of the Effect of Carbohydrate Count on Nutritional Habits and Metabolic Control in Adolescents with Type 1 Diabetes Havva Nur Peltek Kendirci Received Received
  P1-136 Comparison of actual GH dose with labeled dose in children with short stature based on the LG Growth Study Hae Sang Lee Received Received
  P1-137 Persistently increased IGF-I levels and excellent auxological response despite low doses of recombinant growth hormone in a GH-deficient patient with a heterozygous variant of the growth hormone receptor (GHR) gene Maria Laura Nicolosi Received Received
  P2-137 Nutritional evaluation of children with type 1 diabetes on admission to the Endocrinology-Diabetology and Nutrition Department Nisrine Bouichrat Received Received
  P1-138 Safety and effectiveness of pediatric growth hormone therapy: Results from the full cohort in KIGS Mohamad Maghnie Received Received
  P2-138 Correlation between antiinsulin autoantibodies and clinical presentation in T1DM Elena Sukarova-Angelovska Received Received
  P1-139 The effect of growth hormone therapy on linear growth and weight gain in children with growth hormone deficiency vs idiopathic short stature (ISS) ; a controlled study Sohair Elsiddig Received Received
  P2-139 Different schemes of insulin therapy (CSII and MDII) in children with DM1 in a Dnipro city. Viktoria Yenhovatova Received Received
  P1-140 Linear growth response top Growth hormone therapy in underweight versus normal-weight children with idiopathic short stature (ISS). soahir Elsiddig Received Received
  P2-140 HbA1c of T1DM Patients before and after Transition - Single Center Experience Rand Al Harthy Received Received
  P2-141 Glycated Hemoglobin Variability and Microvascular Complications in Patients with Type 1 Diabetes Mellitus Eren Er Received Received
  P1-142 Investigation of primary adrenal insufficiency (PAI) in children with 46,XY differences in sex development (DSD) Elim Man Received Received
  P2-142 Affective response of newly diagnosed Type1 diabetes parents: An experience of a developing country. Aqeela Ayub Received Received
  P2-143 SHORT-TERM GLYCAEMIC CHANGES FROM CONTINUOUS GLUCOSE MONITORING AMONG CHILDREN AND ADOLESCENTS WITH TYPE 1 DIABETES MELLITUS DURING FASTING IN RAMADAN MONTH Sze Teik Teoh Received Received
  P1-143 Current clinical practice of prenatal dexamethasone treatment in at risk pregnancies for classic 21-hydroxylase deficiency in Europe Hanna F. Nowotny Received Received
  P2-144 Is Type 1 Diabetes Mellitus Predictable? Investigation of Predictive Markers n Siblings of Probands with Newly Diagnosed Type 1 Diabetes Mellitus Serpil Albayrak Received Received
  P1-144 Ovarian AMH production is transiently affected in pubertal and prepubertal girls with acute lymphoblastic leukaemia and non-Hodgkin lymphoma receiving chemotherapy: a prospective, longitudinal study. Jimena C. Lopez Dacal Received Received
  P1-145 Serum anti-Mllerian hormone as a marker of ovarian reserve among childhood cancer survivors Silvia Molinari Received Received
  P2-145 Dealing with hypoglycaemia during acute DKA management by paediatric residents from Bahrain, Iraq and Saudi Arabia Hussain Alsaffar Received Received
  P2-146 A Rare Clinical Case Of A Combination Of Monogenic And Autoimmune Diabetes Mellitus. Elizaveta Romanenkova Received Received
  P1-146 Reaching a definitive diagnosis of hypogonadotropic hypogonadism experience of a multidisciplinary diagnostic service Supitcha Patjamontri Received Received
  P2-147 Thrombocytopaenia induced by diazoxide treatment in a toddler with Hyperinsulinism-Hyperammonemia syndrome: a rare side-effect Zacharoula Karabouta Received Received
  P1-147 A pre-analytical challenge to determine estradiol in children: A monovette systematically causing increased estradiol-concentrations in LC-MS/MS analysis Tabea Lamprecht Received Received
  P1-148 Central precocious puberty and sleep patterns in COVID-19 outbreak Anna Grandone Received Received
  P2-148 Nephrotic Syndrome and Type 1 Diabetes: a Therapeutic Approach Beatriz Vala Received Received
  P2-149 Assessment of the percentage of T lymphocytes and B lymphocytes with the expression of ed activation markers in patients with type 1 diabetes mellitus depending on the presence of antibodies against EBV antigens. Izabela Rysz Received Received
  P1-149 QUERY by TELARQUIA: Has there been an increase due to the SARS-COV19 pandemic? Ignacio Diez-Lopez Received Received
  P1-150 Androgen insensitivity without an androgen receptor mutation: results from a large cohort study Nadine Hornig Received Received
  P2-150 PIMS-TS Paediatric Inflammatory Multisystem Syndrome Temporally associated with SARS-CoV-2 (Covid-19) in a child with new onset type 2 diabetes Sophia Sakka Received Received
  P1-151 Duration of Fasting Studies Required to Demonstrate a Cure for Patients with Focal Congenital Hyperinsulinism. Paul S Thornton Received Received
  P2-151 The impact of COVID-19 lockdown on glycaemic control and BMI in children with type 1 diabetes mellitus (T1DM) Saji Alexander Received Received
  P1-152 IMPACT OF GESTATIONAL WEIGHT GAIN ON METHYLATION OF IMPRINTED GENES IN UMBILICAL CORD AND ITS RELATIONSHIP WITH POSTNATAL GROWTH AND METABOLISM Berta Mas-Parés Received Received
  P2-152 Timing of Consulting Paediatric Endocrinologist or Diabetologist During the Management of Acute DKA; Response of Bahraini, Iraqi, and Saudi Paediatric Residents Hussain Alsaffar Received Received
  P1-153 DIFFERENT FACES OF MINIPUBERTY IN PRETERM TWIN GIRLS Giorgia Pepe Received Received
  P2-154 Neonatal Diabetes Secondary to Isolated Pancreatic Agenesis Sarah Bakhamis Received Received
  P1-154 The Evaluation of Accuracy and Effectiveness of Newborn Screening for Congenital Adrenal Hyperplasia in Lithuania Ruta Navardauskaite Received Received
  P2-155 DYSLIPIDEMIA IN CHILDREN WITH TYPE 1 DIABETES MELLITUS Olga Gumeniuk Received Received
  P1-155 Pediatric Inflammatory Multisystemic Syndrome in Brazil: sociodemographic characteristics and risk factors to death Renata Machado Pinto Received Received
  P1-156 Molecular and phenotypic profile of Alstrom syndrome in Chinese patients:results from a Chinese cohort Qianwen Zhang Received Received
  P2-156 THE RELATIONSHIP BETWEEN METABOLIC PARAMETERS,ATHEROGENIC INDEX AND VITAMIN D LEVELS IN CHILDREN WITH INSULIN-DEPENDENT DIABETES MELLITUS Beray SELVER EKL&304;OGLU Received Received
  P2-157 A case of severe hypertriglyceridaemia complicating new-onset type 1 diabetes mellitus Khadidja Belkhatir Received Received
  P1-157 Endocrine Monitoring and Outcome After Therapy In Childhood Survivors of Central Nervous System Tumours Misha Gilani Received Received
  P1-158 Low adrenal androgen levels in patients with and without primary adrenal insufficiency in APECED (APS1) Joonatan Borchers Received Received
  P2-158 A novel variant HNF1A gene (HNF1A-MODY) in a patient presenting with hyperglycaemia and glycosuria Zacharoula Karabouta Received Received
  P1-159 CLINICAL FEATURES AND BODY MINERAL DENSITY IN ITALIAN PATIENTS WITH RAPID ONSET OBESITY WITH HYPOVENTILATION, HYPOTALAMIC DYSFUNCTION, AUTONOMIC DISREGULATION AND NEURAL TUMOR (ROHHADNET): A SINGLE CENTER OBSERVATIONAL STUDY Alessia Angelelli Received Received
  P2-159 Glucose 6 phosphate dehydrogenase deficiency diagnosed with hemolytic anemia triggered by diabetes mellitus type 1 Burce Orman Received Received
  P1-160 Congenital Central Hypothyroidism (CCH) due to a new variant in IGSF1 gene: clinical case of 2 siblings Marco Abbate Received Received
  P2-160 HbA1C stability is posting samples reliable? Nicola Davey Received Received
  P2-161 Not every obese child has type 2 Diabetes Mellitus Diamanto Koutaki Received Received
  P1-161 Continued Safety and Efficacy of Weekly Lonapegsomatropin (TransCon hGH) for up to Two Years in Children with Growth Hormone Deficiency (GHD) Elena Aghajanova Received Received
  P1-162 Evaluation of growth patterns from the Edinburgh and Gothenburg cohorts by the QEPS model Anton Holmgren Received Received
  P2-162 Does insulin pump therapy improve glycaemic control in type 1 diabetes children: one year follow up Najoua MESSAOUDI Received Received
  P2-163 Mauriac syndrome: a complication that still exists in children with type 1 diabetes. Report of a case. Catalina Jiménez Received Received
  P1-163 The aetiology of extreme tall stature in a screened Finnish paediatric population Juho Krkinen Received Received
  P2-164 The Impact of COVID 19 Pandemic on Type 1 Diabetes Mellitus: An experience of a Tertiary Care Hospital in a resource limited country Aqeela Ayub Received Received
  P1-164 Long-term efficacy and safety of rhGH in children with SHOX deficiency: preliminary data of a national Italian survey (on behalf of ISPED Study Group on Growth Factors and Puberty). Patrizia Bruzzi Received Received
  P2-165 Co-existence of new onset diabetic ketoacidosis with severe hypertriglyceridemia in a 9 year old girl. Fatih Kilci Received Received
  P1-165 Eight years of GH treatment in children with PWS: The earlier the start, the better the outcomes? Lionne Grootjen Received Received
  P1-166 The BoneXpert adult height prediction method outperforms the Bayley and Pinneau method in tall male adolescents. Jean De Schepper Received Received
  P2-166 How Does Continuous Glucose Monitoring Systems Effect Metabolic Control In Type 1 Diabetes: Single Center Experience Emrullah Arslan Received Received
  P2-167 Blood level of Vitamin D and metabolic control of type 1 diabetes mellitus Maryam Razzaghy-Azar Received Received
  P1-167 Sex differences in growth response to GH treatment: more prepubertal and less pubertal gain in girls diagnosed with IGHD, ISS, SGA. Analysis of data from GH-SAFETY-database, including all children treated with rhGH- 1986-2009 in Sweden, in National-GH-Reg Elena Lundberg Received Received
  P2-168 Newly-onset type 1 diabetes mellitus triggered by COVID-19: Original case report Salma Benyakhlef Received Received
  P1-168 Mothers smoking during pregnancy influence intrauterine and postnatal growth - the GrowUp 1990 Gothenburg cohort population Kerstin Albertsson Wikland Received Received
  P1-169 Safety of growth hormone and cardiovascular outcomes in patients with Noonan syndrome enrolled in NordiNet International Outcome Study (IOS) and the ANSWER Program Michel Polak Received Received
  P2-169 Case of HNF1B MODY Viktoria Yenhovatova Received Received
  P2-170 Diabetes Ketoacidosis Recovery in Youth with Newly Diagnosed and Established Type 1 Diabetes Keren Smuel Zilberberg Received Received
  P1-170 Facilitating Telehealth In A Tertiary Paediatric Endocrine Service: A Quality Improvement Initiative To Reduce The Discrepancy Between Parent-reported And Auxologist Height Measurements Sinead McGlacken-Byrne Received Received
  P2-171 Association of calprotectin with obesity in prepubertal children Jong Seo Yoon Received Received
  P1-171 Diagnosing growth hormone deficiency - Can a combined arginine and clonidine stimulation test replace two separate tests? Tal Oron Received Received
  P1-172 Glucagon Testing of Childhood-Onset Growth Hormone Deficiency during Transition Davide Guglielmi Received Received
  P2-172 Metabolic syndrome and birth anthropometric data in Prader-Willi syndrome. Alessandro Salvatoni Received Received
  P2-173 Evaluation of the BigO system during the COVID-19 outbreak in Greece Athanasia Tragomalou Received Received
  P1-173 Growth hormone receptor 6O pseudoexon activation: a novel cause of severe growth hormone insensitivity Emily Cottrell Received Received
  P2-174 THE RELATIONSHIP BETWEEN SLEEP TIME AND OBESITY IN CHILDHOOD Ekin Zeynep Altun Received Received
  P1-174 High incidence and male predominance of transient form of isolated growth hormone (GH) deficiency in children. What is the optimal time for GH therapy withdrawal and retesting? Joanna Smyczynska Received Received
  P1-175 GROWTH WITHOUT GROWTH HORMONE. A TERTIARY CARE HOSPITALS EXPERIENCE Sandra Cuenca-Carcelén Received Received
  P2-175 THE RELATIONSHIP BETWEEN ACANTHOSIS NIGRICANS AND VITAMIN D IN OBESE CHILDREN AND ADOLESCENTS Ekin Zeynep Altun Received Received
  P1-176 Irisin in the growth hormone deficient children: before and on rhGH therapy. Wikiera Beata Received Received
  P2-176 Exploring Urinary Bile Acids as Potential Markers of Metabolism: Reference Values in Children by Targeted LC-MS/MS Marcel Schauermann Received Received
  P1-177 Immunogenicity of recombinant growth hormone and relationship its growth-promoting effect in the children with short stature Murat Karaoglan Received Received
  P1-178 Study on linear growth of children with idiopathic short children (ISS) with Low Insulin-like growth factor 1 (IGFI) at diagnosis: Growth hormone (GH) treatment versus no treatment. Sohair Elsiddig Received Received
  P2-179 Frequency of MC4R Pathway Variants in a Large US Cohort of Pediatric and Adult Patients with Severe Obesity Ida Moeller Received Received
  P1-179 Novel dominant negative GH receptor variants provide important insights into GH receptor physiology Afiya Andrews Received Received
  P1-180 The miRNA network and the interplay between growth and cancer regulating pathways in prepubertal patients with idiopathic isolated growth hormone deficiency (IGHD) on growth hormone (GH) treatment Maria Elisabeth Street Received Received
  P2-180 Impact of the COVID-19 pandemic and related lockdown measures on lifestyle behaviours and quality of life in children and adolescents with severe obesity Mila Welling Received Received
  P1-181 Continuous versus discontinuous administration of gonadotropins in neonates with congenital hypogonadotropic hypogonadism Tristan Avril Received Received
  P2-181 Longitudinal association of the anti-inflammatory serum marker GDF-15 with serum IgA and IgG in apparently healthy children Gemma Carreras-Badosa Received Received
  P2-182 Describing the Natural History of Clinical, Biochemical and Radiological outcomes of Children with Familial Partial Lipodystrophy type 2 (FPLD2) attending a National Service for Severe Insulin Resistance: a Retrospective Cohort Study Zhu Xuan Zhong Received Received
  P1-182 Sequence of MKRN3 and DLK1 genes in cases with familial central precocious puberty Esin Karakilic-Ozturan Received Received
  P2-183 Evaluation of the BigO system in a clinical setting in Greece Athanasia Tragomalou Received Received
  P2-184 ASSESSMENT OF DRD2 DOPAMINE RECEPTOR GENE rs6277 IN PEDIATRIC OBESITY: A CASE-CONTROL STUDY Renata Machado Pinto Received Received
  P1-184 The pituitary gonadal axis is not responsive to GnRH administration in PCSK 1 dysfunction Espen Eliyahu Mendelsohn Received Received
  P1-185 Puberty and pituitary-gonadal axis function after treatment for a childhood brain tumor Manon Rosimont Received Received
  P2-185 A Comprehensive, Multidisciplinary, Personalized, Lifestyle Intervention Program is Associated with Increased Leukocyte Telomere Length in Children and Adolescents with Overweight and Obesity George Paltoglou Received Received
  P2-186 Diagnostic accuracy of Tri-Ponderal mass index (kg/m3) for identifying glucose intolerance in obese children and adolescents. Larry Arciniegas Received Received
  P1-186 Serum Testosterone and Estradiol Serve as Markers of Growth Response During Puberty Promoting Treatment &8203; Heta Huttunen Received Received
  P1-187 The Adrenal Steroid Profile in Adolescent Depression: A Valuable Bio-Readout? Raphael Hirtz Received Received
  P2-187 EFFECT OF SEMAGLUTIDE ON BODY WEIGHT IN OBESE CHILDREN WITH CRANIOPHARYNGIOMA : A PRELIMINARY REPORT Marie Jourdren Received Received
  P1-188 Congenital hypogonadotropic hypogonadism in a large French cohort : New genetic findings Abir Talbi Received Received
  P2-188 Development of a predictive normogram to assess the risk of liver steatosis in childhood obesity Gabriel Á. Martos-Moreno Received Received
  P2-189 Prospective evaluation of liver stiffness in obese children: the role of shear wave elastography. Domenico Corica Received Received
  P1-189 Dimensional changes in structures of craniofacial and brain in precocious puberty: Developmental surrogate markers of the brain as a secondary sex characteristic in puberty Murat Karaoglan Received Received
  P1-190 Six novel variants in the MKRN3 gene causing central precocious puberty: characteristics of ten patients and their affected relatives Caroline Gernay Received Received
  P2-190 Evaluation of the nutritional behavior of small and large for gestational age children Anzhalika Solntsava Received Received
  P2-191 Resting energy expenditure and body composition in children and adolescents with severe obesity due to (suspected) medical causes: comparison between different subtypes of obesity Ozair Abawi Received Received
  P1-191 The Impact of Hospital Surgical Volume on Healthcare Utilisation Outcomes after Paediatric Thyroidectomy Alexander Chesover Received Received
  P1-192 Analysis of hypothyroidism NGS test in Korean patients with congenital hypothyroidism in a single center So Yoon Jung Received Received
  P2-192 Exercise-induced expression of myokines in adolescents with simple obesity. Yulia Kasyanova Received Received
  P1-193 Further evidence that Borealin/CDCA8 is involved in thyroid morphogenesis and aging Aurore Carré Received Received
  P2-193 Early decline in sertoli cell function during puberty in overweight and obese boys : a cross-sectional study solène Rérat Received Received
  P1-194 Role of Next Generation Sequencing in the etiological diagnosis of congenital hypothyroidism with gland in situ Valeria Di Natale Received Received
  P2-195 Assessment of Hyperphagia in Patients with Monogenic Obesity Stefanie Zorn Received Received
  P2-196 Machine Learning Quest for Predictive Markers of Lifestyle Modification Outcomes in Pediatric Obesity Treatment Aneta Gawlik Received Received
  P1-196 Clinical and Molecular Presentation of Congenital Hypothyroidism Caused by Thyroglobulin Gene Mutations Sarah Bakhamis Received Received
  P1-197 MANAGEMENT OF NEWBORNS BORN TO MOTHERS WITH AUTOIMMUNE HYPOTHYROIDISM Paolo Cavarzere Received Received
  P2-197 TRIPONDERAL MASS INDEX FOR THE CATEGORISATION OF CHILDHOOD OBESITY ON THE BASIS OF 58.364 OBSERVATIONS OF 7.792 PATIENT Raquel Corripio Received Received
  P2-198 Successful weight loss and resolution of hepatic fibrosis in a girl with severe obesity Louise Apperley Received Received
  P1-198 Novel single nucleotide variation in DUOX2 and NPTX1 genes in two Sardinian sisters with transient congenital hypothyroidism Anastasia Ibba Received Received
  P1-199 New p.Ser237Asn Activating Mutation At The TSHR Receptor, Causing Familial Non- Autoimmune Hyperthyroidism Artur Bossowski Received Received
  P2-199 Association of Thyroid-Stimulating Hormone and Free Thyroxine Concentrations with Cardiometabolic Risk Factors in Euthyroid Obese Children and Adolescents with Metabolic Syndrome NANSY TRAGOMALOU Received Received
  P1-200 Functional studies of PAX8 gene variants in patients affected by congenital hypothyroidism with eutopic thyroid gland Núria Camats Received Received
  P2-200 Impact of weight loss on gonadic function in overweight and obese boys solène Rérat Received Received
  P2-201 Weight status and body composition of children and adolescents during the COVID-19 pandemic Avivit Brener Received Received
  P2-202 The challenges faced in the management of Congenital Generalized Lipodystrophy. Yasmine Abdelmeguid Received Received
  P2-203 ANTHROPOMETRIC AND CLINICAL SITUATION IN TWO GROUPS OF YOUNG ADULTS BORN SMALL FOR GESTATIONAL AGE ( A GROUP WITH CATCH-UP AND ANOTHER WITHOUT CATCH-UP AND TREATED WITH GROWTH HORMONE) Amaya Vela Received Received
  P2-204 Changes in objectively measured physical activity after 2-year lifestyle intervention in pediatric patients with abdominal obesity Maria Cristina Azcona-Sanjulian Received Received
  P2-205 Assessment of cardiometabolic risk factor clustering in obese children and adolescents with metabolic syndrome NANSY TRAGOMALOU Received Received
  P2-206 HOMA-IR in obese children with BMI =2.5SDS, but not 2.5SDS, differ significantly from normal weight children Sofia Leka-Emiri Received Received
  P2-207 Restriction of physical activity is the main cause of childhood obesity during the COVID-19 pandemic reflections from a study conducted in 3 clinical centers in southern Poland Agnieszka Zachurzok Received Received
  P2-208 OSAS in childhood obesity is a more frequent and earlier complication than expected Giulio Maltoni Received Received
  P2-209 A novel homozygous variant of the leptin receptor (LEPR) gene causing familiar early-onset severe obesity in two siblings Silvia Molinari Received Received
  P2-210 Sleep quality and metabolic syndrome in pediatric patients with abdominal obesity María Cristina Azcona-Sanjulian Received Received
  P2-211 The lockdown effects on a pediatric obese population in the COVID-19 era Federica DAmico Received Received
  P2-212 The Relationship between Acanthosis Nigricans and Vitamin D Levels in Obese Children Beray Selver Eklioglu Received Received
  P2-213 Influence of birth weight on cardiovascular risk factors in obese children and adolescents Chiara Guzzetti Received Received
  P2-214 A study on the Complications associated with Severe Obesity in Children and Young People Louise Apperley Received Received
  P2-215 The Effectiveness of Indigenous Knowledge-Based Lifestyle Interventions in Preventing Obesity and Type 2 Diabetes Mellitus in Indigenous Children in Canada: A Systematic Review Maya Kshatriya Received Received
  P2-216 The effects of dextroamphetamine treatment in children with hypothalamic obesity Mila Welling Received Received
  P2-218 Impact of overweight and obesity in pediatrics. Metabolic syndrome and its components Ignacio Diez-Lopez Received Received
  P2-219 What do lipids tell us about the pandemic? Myrna Campagnoli Received Received
  P2-221 Sleep Properly, Reduce Intake, aNd Get Stepping (SPRINGS): a multidisciplinary approach to managing paediatric morbid obesity with severe obstructive sleep apnoea Katherine Hawton Received Received
  P2-222 Design of a Phase 2, Double-Blind, Placebo-Controlled Trial of Setmelanotide in Patients With Genetic Variants in the Melanocortin-4 Receptor Pathway Cecilia Scimia Received Received
  P2-223 Absence of dyslipidemia in obese children with BMI =2.5SDS and similar lipidemic profile to those with BMI 2.5SDS or normal weight Sofia Leka-Emiri Received Received
  P2-224 Inflammation associated to body composition in European prepubertal children: Results from the IDEFICS study Pilar Argente Received Received
  P2-226 THYROID FUNCTION IN YOUTH WITH METABOLIC SYNDROME Olena Tolstikova Received Received
  P2-227 Global survey study of awareness, care and treatment of adolescents living with obesity, their caregivers and healthcare professionals: ACTION Teens Jason C.G. Halford Received Received
  P2-228 Lifestyle habits, consumption of non-nutritive sweeteners and obesity in students and young adults population in Latvia. Zane Roze Received Received
  P2-229 Influence of the basal metabolic profile on the evolution of the pediatric patient with obesity Ignacio Diez-Lopez Received Received
  P2-230 The utility of continuous glucose monitoring systems in the management of children with persistent hypoglycaemia Sathyakala Vijayanand Received Received
  P2-231 Hyperinsulinaemic hypoglycaemia as a MEHMO syndrome component: a case report Diliara Gubaeva Received Received
  P2-232 METHYLATION OF UMBILICAL CORD GENES ASSOCIATES WITH GESTATIONAL WEIGHT GAIN AND OFFSPRINGS CARDIO-METABOLIC PROFILE Berta Mas-Parés Received Received
  P2-233 DIAZOXIDE RESPONSIVE CONGENITAL HYPERINSULINISM Nikhil Lohiya Received Received
  P2-234 Continuous Glucose Monitoring (CGM) Reveals Undertreated Hypoglycemia in Patients with Congenital Hyperinsulinism Davelyn Hood Received Received
  P2-235 A Selective Nonpeptide Somatostatin Receptor 5 (SST5) Agonist Effectively Decreases Insulin Secretion in a KATPHI Mouse Model and in Human HI Islets Diva De Leon Received Received
  P2-236 PLACENTAL FRAT-1 METHYLATION IN WOMEN WITH GESTATIONAL OBESITY IS ASSOCIATED WITH THE BODY COMPOSITION IN THE OFFSPRING AT 6 YEARS OF AGE Ariadna Gómez-Vilarrubla Received Received
  P2-237 PLACENTA N-6/N-3 PUFA RATIO IS ASSOCIATED WITH VISCERAL ADIPOSITY AND CARDIOVASCULAR RISK IN THE OFFSPRING AT 6 YEARS OF AGE Ariadna Gómez-Vilarrubla Received Received
  P2-238 Analysis of Placental Steroidogenesis as a Cause of Recurrent Miscarriage Jenifer Suntharalingham Received Received
  P2-239 Antenatal Markers Related to Fetal Growth Restriction Can Predict Childhood Systolic Blood Pressure Reena Perchard Received Received
  P2-240 Hypomethylation of the Prader-Willi imprinting control region associates with postnatal growth and visceral adiposity in healthy children Gemma Carreras-Badosa Received Received
  P2-241 Incidence of early neonatal hypoglycemia and some related risk factors in Qatar. A cohort study over two years (2018 and 2019) Noor Hamed Received Received
  P2-242 Long-term follow-up in a case with congenital hyperinsulinemic hypogliycemia with a novel p.Ser1389Pro mutation in ABCC8 gene Glin Karacan Kkali Received Received
  P2-243 Postnatal linear growth and weight gain in infants of non-diabetic mothers (INDM) who were born preterm or near term and had significant neonatal hypoglycemia. Nada Alaaraj Received Received
  P2-244 Genetic Testing Access and Results for Patients with Congenital Hyperinsulinism as Conducted through the CHI and University of Exeter Partnership Tai Pasquini Received Received
  P2-245 Predictors of short stature in intrauterine growth retardation in a region of north Africa Bouferoua Fadila Received Received
  P2-246 Massive Open Online Learning accelerating knowledge in digital health in the management of children with growth disorders Paul Dimitri Received Received
  P2-247 A girl with concurrent congenital adrenal hyperplasia, isolated growth hormone deficiency type II (IGHD II) and a new mutation in the GH 1 gene an extremely unusual case Nora Genthner Received Received
  P2-248 Reduction in pappalysin and stanniocalcin levels explain the decrease in IGF-I bioavailability in anorexia nervosa Álvaro Martín-Rivada Received Received
  P2-250 Patterns of non-adherence to growth hormone treatment in children living in Italy Chiara Centonze Received Received
  P2-251 Screening of celiac disease among children with growth hormone deficiency and idiopathic short stature Amany El-Hawary Received Received
  P2-252 Pappalysins and stanniocalcins in prenatal and postnatal life Álvaro Martín-Rivada Received Received
  P2-253 GROWPATI Study: Growth and puberty description pattern in a well-characterized cohort of patients with growth retardation due to severe primary IGF1 deficiency Athanasia Stoupa Received Received
  P2-254 Clinic, laboratory and prognostic findings of patients who are diagnosed by kowarski syndrome (biologically inactive growth hormone) Mehmet Keskin Received Received
  P2-255 NadaPrevalence of insulin-like growth factor 1 (IGF1) deficiency in prepubertal children with isolated short stature (ISS) and their response to GH therapy. Sohair Elsiddig Received Received
  P2-256 Thyroid function (TF)in short children with idiopathic short stature (ISS) treated with growth hormone (GH)versus those not treated; a controlled study. Nada Alaaraj Received Received
  P2-257 Investigating the impact of the TuiTek patient support programme, designed to support caregivers of children prescribed recombinant human growth hormone treatment for growth hormone deficiency in Taiwan: A pilot study Yen-Fan Lin Received Received
  P2-258 Incidence of ALS deficiency in patients with growth hormone deficiency at tertiary pediatric endocrinology center Kamelia Rankova Received Received
  P2-259 Presentation of IGF-1/IGFBP-3 molar ratio as an effective monitoring index during treatment of growth hormone deficient patients Kamelia Rankova Received Received
  P2-260 Current growth hormone therapy practices in Belgium for the treatment of short children born small for gestational age Muriel Thomas Received Received
  P2-261 Increased height and IGF1 serum levels in children with non-neurofibromatosis type 1 gliomas Florencia Clément Received Received
  P2-262 A Survey on Clinician Perceptions of Long-Acting Growth Hormone Analogs Naomi Howard-James Received Received
  P2-263 Pituitary gland volume measured by Magnetic Resonance Imaging as diagnostic predictor of persistent Childhood-onset growth hormone deficiency Beatriz Corredor-Andres Received Received
  P2-264 Growth hormone (GH)treatment of children with idiopathic short children (ISS) with normal insulin-like growth factor-1( IGF-1) versus those with low IGF-I at diagnosis. Sohair Elsiddig Received Received
  P2-265 Growth response to growth hormone therapy in growth hormone deficient (GHD) children in relation to the distance between their height SDS (HtSDS) and their mid-parental height. Sohair Elsiddig Received Received
  P2-266 Linear growth and response to GH therapy in children with short stature with normal Growth hormone secretion: Comparison between children with delayed versus no delay in the bone age at diagnosis. Nada Alaaraj Received Received
  P2-267 Linear growth and response to GH therapy in children with GHD with normal IGF-I versus those with normal GH secretion associated with low IGFI at presentation. Sohair Elsiddig Received Received
  P2-268 Growth response to growth hormone therapy in short children in relation to their distance from mid-parental heights (MPHt). Sohair Elsiddig Received Received
  P2-270 Unified training materials to improve adherence to GH-treatment Elena Lundberg Received Received
  P2-271 Linear growth of prepubertal children born small for gestational age on growth hormone therapy for 3 years Adnan Al Shaikh Received Received
  P2-272 Evaluation of the clinical and laboratory parameters and final adult height in patients treated with recombinant human growth hormone. Ayca Altincik Received Received
  P2-273 THE RESULTS OF TREATMENT WITH GROWTH HORMONE IN A PATIENT WITH GROWTH HORMONE DEFICIENCY AND TYPE 1 DIABETES Anna Rakus-Kwiatosz Received Received
  P2-274 Aetiology and different clinical conditions of GHD in children in a region of North Africa Bouferoua Fadila Received Received
  P2-276 Growth Hormone Resistance; The Iraqi experience Ali Al-Jumaili Received Received
  P2-277 Response to growth hormone therapy with high IGF-1-levels and severe insulin resistance in two-cases with SOFT syndrome: A novel homozygous mutation in POC1A Esin Karakilic-Ozturan Received Received
  P2-278 Effects of growth hormone therapy on serum concentrations of IGF-1 in patients with Turner syndrome: High IGF-1 concentrations despite optimal dose? Esin Karakilic-Ozturan Received Received
  P2-279 The Effect of Hospital Admission and Nutritional Rehabilitation (NR) on Growth and Metabolic abnormalities in adolescent females with severe Anorexia Nervosa (AN) Nada Alaaraj Received Received
  P2-280 Outcomes in growth hormone-treated Noonan syndrome children: impact of PTPN11 mutation status Alexander Jorge Received Received
  P2-281 ENDOCRINOLOGICAL ASSESSMENT IN PATIENTS WITH FANCONI ANEMIA Beatriz Corredor-Andrés Received Received
  P2-282 Brain-derived neurotrophic factor and matrix metalloproteinases as markers of metabolic status in girls with Turner syndrome. Ewa Blaszczyk Received Received
  P2-283 Assessment of genetic defects, baseline characteristics and adverse events reported in the Increlex registry Amelia Frizell-Armitage Received Received
  P2-284 Associations between height and health-related quality of life (HRQoL) and functional independence in children with achondroplasia Melita Irving Received Received
  P2-285 COVID 19 impact on Pediatric Endocrinology care a short story from Romania Raluca Pop Received Received
  P2-287 Novel LZTR1 mutations in subjects with features of Noonan Syndrome and GH insensitivity negatively regulate GH-induced IGF-I production and hyperactivate GH-induced ERK1/2 activation in response to GH in vitro Sumana Chatterjee Received Received
  P2-288 COMORBIDITIES IN TURNER SYNDROME PATIENTS CONTROLLED IN OUR CENTER SINCE THE 80s Raquel Corripio Received Received
  P2-289 Familial Mosaic Turner Syndrome with short stature and spontaneous puberty due to a ring X chromosome with distal Xp22.3 and distal Xq26 deletion Sharon Lim Received Received
  P2-290 Linear growth response to growth hormone therapy in underweight versus normal-weight children with idiopathic short stature (ISS) Sohair Elsiddig Received Received
  P2-291 Linear Growth and Weight gain in Infants with Significant Neonatal Hypoglycemia during the first two years of age: Comparison of infants of Diabetic Mothers (IDM) versus infants of non-diabetic mothers (INDM) with transient hyperinsulinemia (non-ketotic) Nada Alaaraj Received Received
  P2-292 Timing of infancy-childhood growth spurt in healthy Turkish children Oya Ercan Received Received
  P2-293 Effects of GH replacement therapy on body composition and muscle health in children and adolescents with GH deficiency: one-year prospective case-control study. IMPRODA NICOLA Received Received
  P2-294 The spectrum of the Prader-Willi-like pheno- and genotype Alicia Juriaans Received Received
  P2-295 An Italian survey on GH stimulation tests and their adverse side effects. Alessandro Salvatoni Received Received
  P2-296 Comparing the efficacy of nutritional supplementation of different caloric concentrations on linear growth and weight gain in late childhood, a longitudinal study. Nada Alaaraj Received Received
  P2-297 The efficacy and safety of recombinant biosimilar growth hormone treatment in children with GHD and SGA: a Czech retrospective national longitudinal study Marta Snajderova Received Received
  P2-299 Case report: Tall stature, obesity and hip dysplasia in Weaver syndrome due to a loss-of-function variant in EHZ2 Niki Paraskevopoulou Received Received
  P2-300 Association of Daily Growth Hormone Injection Adherence and Height among Children with Growth Hormone Deficiency Jane Loftus Received Received
  P2-301 The evaluation of growth velocity, height, weight, elementary laboratory tests and hormonal function in the patient with Floating-Harbor syndrome treated with growth hormone for 20 months case report, preliminary report. Maja Oko&324;ska Received Received
  P2-302 Two Sibling Cases with Growth Hormone Receptor Mutation: Variable Clinical Expressivity in Laron Syndrome Behiye Sar&305;kaya zdemir Received Received
  P2-303 A literature review of the potency and ivity of FGFR-ive tyrosine kinase inhibitors, such as infigratinib, in the potential treatment of achondroplasia Lee Miller Received Received
  P2-304 Impact of estrogen therapy on pubertal growth in Turner syndrome Marie-Agathe Trouvin Received Received
  P2-305 ANASTROZOLE IMPROVES HEIGHT PREDICTION AND NEAR FINAL HEIGHT AS MONOTHERAPY OR IN COMBINATION WITH GROWTH HORMONE Renata Machado Pinto Received Received
  P2-306 Growth hormone deficiency (GHD) with high circulating insulin-like growth factor-1 (IGF-1) in an adolescent with celiac disease: Is it IGF-1 insensitivity? Nada Alaaraj Received Received
  P2-307 Postnatal Linear Growth and Weight Gain in Infants of Diabetic Mothers (IDM) Who Were Born at or Near Term and Had Severe Neonatal Hypoglycemia Without Other Comorbidities. Nada Alaaraj Received Received
  P2-308 Evidence that non-syndromic familial tall stature has an oligogenic origin including ciliary genes Gudrun A. Rappold Received Received
  P2-309 Early-onset growth hormone treatment in Prader-Willi syndrome attenuates the risk of transition to severe obesity Aneta Kodytková Received Received
  P2-310 Incidental pituitary adenoma detection in two patients affected by Williams Syndrome: only a coincidence? Silvia Ciancia Received Received
  P2-311 Efficacy of recombinant growth hormone therapy in TRPS 1 syndrome coexisting with growth hormone deficiency. Kamil Dyrka Received Received
  P2-312 Results from the Implementation of a Growth Disorders Related Twinning Programme (Partners4Growth) at tertiary pediatric endocrinology clinics Stanimira Elkina Received Received
  P2-313 CO-OCCURRENCE OF TURNER (46,X-ring/45,X0 MOSAICISM) AND MAYER-ROKITANSKY-KUSTER-HAUSER SYNDROMES: A CASE REPORT. Laura Ocello Received Received
  P2-314 Shox Gene Pathologies In Children With Short Stature And Madelung Deformity Merve Sakar Received Received
  P2-315 Characteristics of Patients with Noonan Syndrome Carrying a PTPN11 Mutation: The Recombinant Growth Hormone Treatment and Long-Term Follow-up Glin Karacan Kkali Received Received
  P2-316 DETERMINING FACTORS OF A GOOD RESPONSE TO TREATMENT WITH GROWTH HORMONE FOR THE FIRST 2 YEARS Antonio de Arriba Received Received
  P2-317 Noonan syndrome patients with short stature at a single pediatric endocrinology centre Yana Deyanova Received Received
  P2-319 Rare case report: A Chinese boy with MDPL syndrome cause by POLD1 gene mutation Qiuli Chen Received Received
  P2-320 An Unusual Case of Gastrointestinal Bleeding: Expecting the Unexpected Sarah Brooke Received Received
  P2-321 Alterations in Metabolic profile and Body Composition in children with Silver Russell syndrome GIUSEPPA PATTI Received Received
  P2-322 Growth abnormalities in patients with Type 1 diabetes Najoua MESSAOUDI Received Received
  P2-323 A novel CEP57 mutation of mosaic variegated aneuploidy syndrome in a Chinese girl:a case report and review of literature Biyun feng Received Received
  P2-324 A Patient with Turner Syndrome (45X/46XX) and Congenital Adrenal Hyperplasia: A Case Report and Literature Review yirou wang Received Received
  P2-325 Impact of oral nutritional supplements on growth outcomes in underweight children (5: 12 years) with no systemic disease. Nada Alaaraj Received Received
  P2-326 Differential diagnosis of pre- and postnatal short stature revisited: 3-M syndrome Platonas Karatsiolis Received Received
  P2-327 A case of a Floating-Harbor syndrome in a child with severe short stature. Anna Prosvirnina Received Received
  P2-328 Excessive body hair, short stature and advanced bone age in a girl : Hypertrichosis versus adrenarche? Shayma Ahmed Received Received
  P2-329 CORNELIA DE LANGE SYNDROME: A CASE REPORT Marouan Karrou Received Received
  P2-330 Short stature and efficacy of growth hormone treatment in a child with Nail-Patella Syndrome. A case report. Maria Pankratova Received Received
  P2-331 Final and Near-final Adult Height and BMI after Long-term Growth Hormone Treatment in Patients with Turner Syndrome (TS) Adnan Al Shaik Received Received
  P2-332 Evaluating Safety, Efficacy, and Pharmacokinetics of Weekly TransCon CNP in Children with Achondroplasia: Design of the ACcomplisH Trial Ciara Mcdonnell Received Received
  P2-333 An Early Diagnosis of Prohormone Convertase Deficiency Selin Elmaogullari Received Received
  P2-334 Serologic Testing for Celiac Disease and Gluten Intolerance in a Singaporean paediatric endocrine and growth clinic. Warren Lee Received Received
  P2-335 Obesity, vaginal bleeding and ovarian mass in a 5-year-old female girl with autoimmune hypothyroidism Shaymaa Elsayed Received Received
  P2-336 Endocrine and metabolic complications according to genotype in Prader-Willi syndrome Ju Young Yoon Received Received
  P2-337 Van Wyk-Grumbach Syndrome in an Egyptian Female Pediatric Patient: a rare presentation of a common disease Amany Ibrahim Received Received
  P2-338 Diagnostic and Follow-up Problems of Medical Care for Prader-Willi Syndrome Children in Resourse-Limited Settings Natallia Akulevich Received Received
  P2-339 THREE GENERATIONS OF MEN-1: THE IMPORTANCE OF FAMILY SCREENING Julia Galhardo Received Received
  P2-340 Follow-up and management of endocrine and metabolic disorders after hematopoietic stem cell transplantation in a patient followed for Fanconi anemia Najoua Lassoued Received Received
  P2-341 Neonatal McCune Albright Syndrome Presenting with Diabetes Mellitus Yagmur nsal Received Received
  P2-342 Combined pituitary hormone deficiency associated with Graves disease Najoua Lassoued Received Received
  P2-343 Autoimmune polyendocrine syndrome type 2 and precocious puberty: a rare association Imane Assarrar Received Received
  P2-344 Thermoregulatory delays in Greek PCOS adolescents Flora Bacopoulou Received Received
  P2-345 Endocrine manifestations in familial neurofibromatosis type 1: a case report Younes Ayadi Received Received
  P2-346 The clinical and biochemical spectrum of pituitary lesions in children compared to adults: experience from a single tertiary center Elena Galazzi Received Received
  P2-347 Optic tract glioma and endocrine disorders- comparison between patients with and without NF1- a single center experience Merav Gil Margolis Received Received
  P2-348 ENDOCRINE MANIFESTATIONS OF PAEDIATRIC INTRACRANIAL GERM CELL TUMOUR: FROM DIAGNOSIS TO LONG-TERM FOLLOW-UP Cristina Partenope Received Received
  P2-349 Machine learning to detect the Klinefelter syndrome endocrine profile André Madsen Received Received
  P2-350 Nuchal Skinfold Thickness in Pediatric Brain Tumor Patients Hermann L. Mller Received Received
  P2-351 Growth hormone deficiency in 52 children with brain Magnetic Resonance Imaging Abnormalities OUIDAD BAZ Received Received
  P2-352 Patients with PWS and related syndromes display differentially methylated regions involved in neurodevelopmental and nutritional trajectory. Juliette Salles Received Received
  P2-353 CLINICAL COURSE OF PRIMARY EMPTY SELLA IN CHILDREN: A 10-YEAR SINGLE-CENTER EXPERIENCE Ozge Besci Received Received
  P2-354 Relation between specific pubertal growth and breast maturation - a longitudinal study in healthy girls Sophie Bergendahl Received Received
  P2-355 Did Central Precocious Puberty Increase in COVID 19 Pandemic? Burce Orman Received Received
  P2-356 DELAYED DIAGNOSIS OF PAEDIATRIC INTRACRANIAL GERM CELL TUMOUR (IC-GCTs) Cristina Partenope Received Received
  P2-357 Gonadotropin-releasing hormone analog treatment in children with idiopathic central precocious puberty: a pharmacovigilance study in a pediatric population. Chiara Nasso Received Received
  P2-358 Pubertal induction in girls with hypogonadism: preliminary prospective data of efficacy in patients with/without initial overnight estrogen replacement Giulia Rodari Received Received
  P2-359 EVALUATION OF PITUITARY/CRANIAL IMAGING RESULTS OF CENTRAL PUBERTE PRECOCIOUS CASES Havva Nur Peltek Kendirci Received Received
  P2-360 In vivo magnetic resonance spectroscopy as a non-invasive tool for the identification of a sellar tumour in a boy with precocious puberty. Ioanna Kosteria Received Received
  P2-361 Rahman Syndrome: Hypopituitarism might be responsible for changing height pattern Sare Kaygusuz Received Received
  P2-362 CONGENITAL HYPOPITUITARISM: THE ROLE OF GENETICS Estela Gil Poch Received Received
  P2-363 Pedigree analysis is essential for clarifying oligogenic transmission in a family with congenital hypogonadotropic hypogonadism (CHH) Sarah Oberhauser Received Received
  P2-364 Congenital hypogonadotropic hypogonadism associated with X-linked ichthyosis due to X-chromosome microdeletion identified by chromosomal microarray Kristina Kokoreva Received Received
  P2-365 Gonadotropin Flare with Different Depot GnRH Agonists: Comparative Analysis. Analía Freire Received Received
  P2-366 HYPOTHALAMIC OBESITY IN CHILDREN WITH CRANIOPHARYNGIOMA Ouidad Baz Received Received
  P2-367 Duplication of Pituitary Gland-plus Syndrome presenting with a Transcranial Nasal Dermoid Cyst Manju Chandwani Received Received
  P2-368 Sterile Abscess Formation with Two Different GnRH Analogues: Three Case Reports Glin Karacan Kkali Received Received
  P2-369 6-Month GnRHa Formulations Are a Good Choice During the COVID-19 Pandemic and Beyond Matthew Benson Received Received
  P2-370 Size Matters: CAG Repeat Length of the Androgen Receptor Gene, Testosterone, and Male Adolescent Depression Severity Raphael Hirtz Received Received
  P2-371 Is quail egg a potential endocrine disrupter ? Sare Kaygusuz Received Received
  P2-372 The impact of the Covid-19 pandemic on the UK National Hypothalamic-pituitary Axis Tumour (HPAT) multidisciplinary meeting Laura Bosch i Ara Received Received
  P2-373 Evaluation of Clinical, Laboratory and Radiological Findings in the Differential Diagnosis of Premature Telarche and Central Puberty Precocious Havva Nur Peltek Kendirci Received Received
  P2-374 Crooke Cell Adenoma as a Rare Cause of Recurrent Cushing Disease: A Challenge in Treatment and Follow-up Arzu Jalilova Received Received
  P2-375 Salivary sex steroids as markers of puberty in boys during late childhood and adolescence Supitcha Patjamontri Received Received
  P2-376 Efficacy of cabergoline in the treatment of pituitary macroadenoma complicated in a 14-year-old girl. Anouar Jamal Received Received
  P2-377 USE OF TOLVAPTAN IN A CHILD WITH SIADH POST PITUITARY SURGERY Nikhil Lohiya Received Received
  P2-378 The effect of 3 years of Gonadotropin-Suppressive Therapy in Girls with Early Puberty: Height Z Score in Relation to Mid-Parental height Z score. Nada Alaaraj Received Received
  P2-379 An Observational, Retrospective Study to Evaluate Long Term Safety and Effectiveness of Leuprorelin in the Treatment of Central Precocious Puberty Junfen Fu Received Received
  P2-381 Characterization of puberty development in a large cohort of patients with Noonan syndrome with molecular diagnosis Raíssa Rezende Received Received
  P2-382 Pituitary tumors in children and adolescents: clinical and etiological profile Nisrine Bouichrat Received Received
  P2-383 Langerhans Cell Histiocytosis with Isolated Central Diabetes Insipidus, Low Grade Fever and Sellar Erosion Iclal Okur Received Received
  P2-384 Basal LH as a screening test for diagnosis of central precocious puberty Shaymaa Raafat Mahfouz Received Received
  P2-386 Blood Pressure in Girls with Central Precocious Puberty and GnRH Analog Therapy Naama Fisch Shvalb Received Received
  P2-387 Isolated central diabetes insipidus and periventricular nodular heterotopia in a 9-year-old girl Florentina Haufler Received Received
  P2-388 Central precocious puberty: clinical, etiologic and therapeutic features Imane Assarrar Received Received
  P2-389 Atypical Presentation of Pituitary Macroadenoma in an adolescent girl: Central Hypothyroidism and Attenuated Pubertal Growth Spurt. Nada Alaaraj Received Received
  P2-390 A case of partially Empty Sella with hypopituitarism in a child Rajat Pratap Received Received
  P2-391 Cushings disease in paediatric patients: Diagnosis and evolution Najoua MESSAOUDI Received Received
  P2-393 First Morning Voided Urinary Gonadotropin Measurements for the Early Screening, Diagnosis and Follow-up of Central Precocious Puberty Patients Feng Ye Received Received
  P2-395 Cognitive function and linear growth in Prednisone -treated children with salt-wasting congenital adrenal hyperplasia Shaymaa Elsayed Received Received
  P2-396 Combining big data science with clinics: Novel approach for understanding human sex development and its variants. Daniel Rodríguez Gutiérrez Received Received
  P2-397 Vascular dysfunction and increased cardiovascular risk in hypospadias Angela Lucas-Herald Received Received
  P2-399 Self-reported Feelings of Adult Patients with Differences of Sex Development (DSD) Regarding Genital Surgical Procedures Berenice Bilharinho de Mendonca Received Received
  P2-401 TWO SISTERS WITH PRIMARY HYPERGONADOTROPIC HYPOGONADISM, PUBERTAL PROGRESS AND DELETION OF 61.5MB OF Xq21.33q28 REGION Eirini Dikaiakou Received Received
  P2-402 DESCRIPTION OF A NEW VARIANT IN THE MAMLD1 GENE IN AN INFANT WITH MICROPHALLUS AND HYPOSPADIAS Cristina Aguilar Riera Received Received
  P2-403 SURGICAL ASPECTS OF THE MULTICENTRIC AND INTERDISCIPLINARY STUDY IN MINORS WITH DIFFERENT SEXUAL DEVELOPMENT Ignacio Diez-Lopez Received Received
  P2-404 Is Inflammation the Major Driver of Polycystic Ovary Syndrome (PCOS)? A Proteomic Approach to Understanding PCOS in Adolescents and the Search for Novel Non-Invasive Biomarkers Harriet Gunn Received Received
  P2-405 Serum High Mobility Group Box 1 (HMGB1) levels are independently associated with glucose clamp-derived measures of insulin resistance in PCOS. Maria Elisabeth Street Received Received
  P2-406 ZSWIM7 is associated with human female meiosis and familial primary ovarian insufficiency Sinead McGlacken-Byrne Received Received
  P2-407 IS THE RECOMMENDED DUAL THERAPY FOR TRANSSEXUAL BOYS HARMLESS? Itxaso Rica Received Received
  P2-408 Plexiform neurofibroma of the penis as an infrequent manifestation debut in a pediatric patient. Fernanda Peña Received Received
  P2-409 Surprising X Chromosomes: Unusual Mosaicism Zeinab Zorkot Received Received
  P2-410 Puberty delay in girls: etiological structure of the disease Kseniya Kabolova Received Received
  P2-411 Rationale for a reduced dexamethasone dose in prenatal congenital adrenal hyperplasia therapy based on pharmacokinetic modelling Uta Neumann Received Received
  P2-412 45,X/46,XY Mosaicism: Phenotypic characteristics, Growth, and Gonadal features. Nalini M Selveindran Received Received
  P2-413 Challenges faced by children and adolescents with Differences in Sex Development (DSD) managed at a tertiary care specialized university center in Sri Lanka. Chamath Jayakody Received Received
  P2-414 A novel mutation of SOX2 gene in an idiopathic hypogonadotropic hypogonadism patient with olfactory bulb agenesis yijun tang Received Received
  P2-415 Obesity, ovarian mass, vaginal bleeding and hypothyroidism in a 5-year-old female girl Noora Alhemaidi Received Received
  P2-416 Ovarian Juvenile Granulosa Cell Tumor in 9-Month-Old female Infant presented with Isosexual Pseudo Puberty: Case Report Shayma Ahmed Received Received
  P2-417 A case report of Non-syndromic 46, XX testicular DSD presenting as a genital ambiguity - Clinical, molecular and cytogenetic analysis kishore behera Received Received
  P2-419 A late revelation of Sexual differentiation disorder 46XX due to 11 beta hydroxylase deficiency Khensal Sabrina Received Received
  P2-421 Radiological evaluation of children with atypical genitalia due to disorders of sex development (46, XY DSD) in a resource-limited setup Doaa Khater Received Received
  P2-422 17 HYDROXYLASE DEFICIENCY AND DIABETES IN A CASE WITH 46 XY FEMALE Ahmet Yildirim Received Received
  P2-423 Diagnostic Dilemma in a Patient with Central Precocious Puberty: Ovarian Steroid Cell Tumor Hanife Gl Balki Received Received
  P2-424 Dimensional approach to Gender Dysphoria in Nigeria: association with socio-demographics and psycho-sexual variables. Ugo Chikani Received Received
  P2-425 Puberty delay in girls: analyses of disease structure depending on clinical characteristics Kseniya Kabolova Received Received
  P2-426 UTERUS AGENESIA IN A PATIENT WITH CATCH 22 SYNDROME. PURPOSE OF A CASE. Ignacio Diez-Lopez Received Received
  P2-427 High throughput screening of DSD candidate genes with the help of the powerful model Drosophila melanogaster Isabel von der Decken Received Received
  P2-428 Case series: Use of tamoxifen in the management of gynaecomastia in three adolescent boys with 46 XY DSD Chamath Jayakody Received Received
  P2-429 4-year-old female patient with mixed germ cell tumor and underlying Cowden syndrome Daniela Habacht Received Received
  P2-430 A COMPARISON BETWEEN ANDROSTANOLONE AND TESTOSTERONE ENANTHATE FOR PENILE AUGMENTATION IN PATIENTS WITH IDIOPATHIC MICROPENIS Marouan Karrou Received Received
  P2-431 Combination therapy of hypogonadotropic hypogonadism with rFSH and hCG case report Kristina Kokoreva Received Received
  P2-432 46,XY DSD due to biallelic DHX37 gene mutations Mehmet Eltan Received Received
  P2-433 Novel Mutation in an Iranian Family with 17- Hydroxysteroid Dehydrogenase Type 3 Deficiency Fatemeh Saffari Received Received
  P2-434 A CASE OF GENDER DEVELOPMENTAL DISORDER WITH DIFFICULTY IN MOLECULAR DIAGNOSIS: NEW VARIANT IN NR5A1 GENE Emrullah Arslan Received Received
  P2-435 Two pedigrees with congenital bilateral anorchia in one sibling and testicular torsion at adolescence in another: a shared genetic predisposition? Cécile Brachet Received Received
  P2-436 Importance of testicular biopsy for validation of diagnosis; cryptorchidism, analyzing prescrotal undescended testes Faruk Hadziselimovic Received Received
  P2-437 Rare Genetic disorder associated with microphallus Khalid Khan Received Received
  P2-438 CONGENITAL ADRENAL HYPERPLASIA IN DETAIL: A MULTICENTRIC AND INTERDISCIPLINARY STUDY IN MINORS WITH DIFFERENT SEXUAL DEVELOPMENT Ignacio Diez-Lopez Received Received
  P2-439 SEX ASSIGNMENT AT BIRTH: IS IT ALWAYS EASY? Marouan Karrou Received Received
  P2-440 Combination therapy of hypogonadotropic hypogonadism in boys with rFSH and hCG case reports analyses Kristina Kokoreva Received Received
  P2-441 Clinical case of premature ovarian failure in combination with blepharophimosis-ptosis-epicanthus inversus due to mutation in FOXL2 gene Sofia Enikeeva Received Received
  P2-442 Persistent Mllerian duct syndrome presenting with bilateral cryptorchidism and obstructed inguinal hernia. Anatoli Fotiadou Received Received
  P2-443 5 ALPHA REDUCTASE TYPE 2 DEFICIENCY: A CASE REPORT Marouan Karrou Received Received
  P2-445 Could intramuscular testosterone differentiate between partial androgen insensitivity and 5 alpha reductase type 2 deficiency? Shaymaa Raafat Received Received
  P2-446 The efficacy and short- and long-term side effects of radioactive iodine treatment in pediatric Graves disease: a systematic review Christiaan Mooij Received Received
  P2-447 Incidentally detected papillary thyroid cancer with elevated calcitonin in a 15 year-old female : a case report Jeesuk Yu Received Received
  P2-448 Methimazole-Induced Remission Rates in Pediatric Graves Disease: a Systematic Review Nitash Zwaveling-Soonawala Received Received
  P2-449 Congenital multinodular goiter causing acute airway obstruction in a newborn: a case report Mirjam Scheffer-Rath Received Received
  P2-450 Initial response to thionamide medication in young people with newly diagnosed thyrotoxicosis. Claire Wood Received Received
  P2-451 A GIRL WITH TRISOMY 21 PRESENTS WITH VAN WYK-GRUMBACH SYNDROME. A RARE DIAGNOSIS Ioanna Kosteria Received Received
  P2-452 Complications after pediatric thyroidectomy: lymph node dissection is a risk factor for permanent hypocalcemia Christiaan Mooij Received Received
  P2-453 Kinetics of FT4 serum concentrations in newborns and infants with congenital hypothyroidism during follow-up differ in the three severity groups Britta Steffens Received Received
  P2-455 Expression of Zinc transporter 8 in thyroid tissues from patient with immune and non-immune thyroid diseases. Artur Bossowski Received Received
  P2-456 HASHIMOTO THYROIDITIS: LONG TERM FOLLOW-UP FROM CHILDHOOD TO YOUNG ADULTHOOD Francesco David Received Received
  P2-457 A case of complete atrioventricular block after initiation of methimazole in a patient with Graves disease associated with Downs syndrome previously undergoing cardiac surgery KENTARO SAWANO Received Received
  P2-458 UNILATERAL AUTOIMMUNE OPHTHALMOPATHY AS A FIRST SYMPTOM IN MANIFESTATION OF AUTOIMMUNE THYROIDITIS AND SYSTEMIC LUPUS ERYTHEMATOSUS IN AN ADOLESCENT GIRL.CASE REPORT. Olena Tolstikova Received Received
  P2-459 Incidence and etiology of primary congenital hypothyroidism in Flanders Sofie Ryckx Received Received
  P2-460 Re-evaluation of the prevalence of permanent congenital hypothyroidism in Niigata, Japan: A retrospective study Keisuke Nagasaki Received Received
  P2-461 EARLY REASSESSMENT IN CONGENITAL HYPOTHYROIDISM Gema Grau Received Received
  P2-462 Growth impairment in children with severe autoimmune primary hypothyroidism and pituitary hyperplasia without goiter. Domenico Corica Received Received
  P2-463 The Use Of Intravenous Introduction Of Glucocorticoids In The Active Stage Of Graves Ophthalmopathy In Childhood. Clinical Case. Tatiana Ivannikova Received Received
  P2-464 Atypical presentation of acute suppurative thyroiditis in a 6 year old child. Maria Liapi Received Received
  P2-465 Allan-Herndon-Dudley syndrome: case report of a rare disorder Irina Muradyan Received Received
  P2-466 Hypothyroidism in context of 1q44 microdeletion syndrome and DOLK-CDG Bogdan Pascu Received Received
  P2-467 Graves Ophthalmopathy in Pediatric Age: Different Severities, Different Approaches David Veríssimo Received Received
  P2-469 Thyroid dysfunction in Beta-thalassemia patients Noumi Mustapha Received Received
  P2-470 VICTIM PATHOLOGIES OF THE PANDEMIC. SEVERE ACQUIRED HYPOTHYROIDISM. Ignacio Diez-Lopez Received Received
  P2-471 Mitigating thyroid cancer risk in multinodular hyperplasia secondary to a 10q23.31 deletion (PTEN Hamartoma Tumour Syndrome) Meera Shaunak Received Received
  P2-472 Thyroid dysfunction and autoimmune thyroiditis in children with new-onset diabetes mellitus Jeesuk Yu Received Received
  P2-473 A Rare Cause of Congenital Hypothyroidism: Brain-Lung-Thyroid Syndrome Aslihan Arasli Yilmaz Received Received
  P2-474 Recurrent fractures in a child with Graves disease Fatih Kilci Received Received
  P2-475 Case study of 13- year-old boy suffering from papillary thyroid cancer in stage pT3aN1bMX. Artur Bossowski Received Received
  P2-476 EVALUATION OF GENERAL CHARACTERISTICS OF CHILDREN WITH HYPOTHYROIDI Beray Selver Eklioglu Received Received
  P2-477 L-T4 absorption test in 14-year-old patient with severe refractory hypothyroidism after total thyroidectomy Gaia Vincenzi Received Received
  P2-478 A child with anti-thyroid arthritis syndrome Fatih Kilci Received Received
  P2-479 Thyroglobulin deficiency: a rare cause of neonatal stridor Xanthippi Tseretopoulou Received Received
  P2-480 TBG deficiency and Central Congenital Hypothyroidism (CCH): Our experience in neonatal screening with TSH and T4 Maria J. Chueca Received Received
  P2-481 A CASE OF HYPOTHYROIDISM POST BONE MARROW TRANSPLANTATION Ouidad Baz Received Received
  P2-485 Prevalence and associated factors of Congenital Hypothyroidism in Bogotá, Colombia. 2014 - 2020 Pablo Pineda Received Received
  P2-486 Aetiology and different clinical condition of hypothyroidism in children and adolescents Fadila Bouferoua Received Received
  P2-487 Influenza A induced Thyrotoxic Storm Post Haematopoietic Stem Cell Transplantation Nuthana Prathivadi Bhayankaram Received Received
  P2-489 Thyrotropic cell hyperplasia secondary to prolonged uncontrolled primary hypothyroidism Ana Belen Ariza Jimenez Received Received
  P2-490 Thyroid dyshormonogenesis: a case report of two siblings with a heterozygous variant in the TPO gene. Tatiana Vadina Received Received
  P2-491 Pediatric Graves disease in southern Tunisia Sana Kmiha Received Received
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59th Annual ESPE Meeting

 

22-26 September 2021 Virtual Conference
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