ESPE Abstracts

EPosters

• HRP0094P1-1

  Optimizing the timing of highest hydrocortisone dose in children and adolescents with 21-hydroxylase deficiency

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• HRP0094P1-2

  Adrenocortical hormone profiles do not predict the molecular etiology in non-CAH primary adrenal insufficiency

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• HRP0094P1-3

  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

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• HRP0094P1-4

  Depression among insured children and young adults in the United States with congenital adrenal hyperplasia

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• HRP0094P1-5

  Alterations in resting-state functional connectivity in patients with congenital adrenal hyperplasia

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• HRP0094P1-6

  International practice of therapy monitoring in congenital adrenal hyperplasia - Real World data from the I-CAH registry

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• HRP0094P1-7

  Brain activity during working memory in congenital adrenal hyperplasia

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• HRP0094P1-8

  Long-term Cardiometabolic Morbidity In Young Adults With Classic 21-Hydroxylase Deficiency Congenital Adrenal Hyperplasia

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• HRP0094P1-9

  Backdoor Pathway hormones and 11-oxygenated Androgens are elevated in Patients with 21-hydroxylase deficiency

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• HRP0094P1-10

  Glucose regulation in children with primary adrenal insufficiency: preliminary data.

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• HRP0094P1-11

  Bone and endocrine monitoring in boys with Duchenne Muscular Dystrophy

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• HRP0094P1-12

  Real-world clinical profiles of children with hypophosphatasia (HPP) from the Global HPP Registry

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• HRP0094P1-13

  Characterisation and phenotype-genotype associations of a large cohort of patients with pseudohypoparathyroidism type 1A and 1B

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• HRP0094P1-14

  Tumor induced osteomalacia, a rare and complex condition with more treatment options, exemplified in two patients.

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• HRP0094P1-15

  Vitamin D status and guidelines in Paediatric Inflammatory Multisystem Syndrome Temporarily associated with SARS-CoV-2 (PIMS-TS)

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• HRP0094P1-16

  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.

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• HRP0094P1-17

  Clinical Spectrum of Hypomagnesemia type 1 (HOMG1) due to Novel <em>TRPM6</em> mutations

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• HRP0094P1-18

  A rare cause of hypercalcemia: Congenital Lactase Deficiency

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• HRP0094P1-19

  Acetazolamide treatment in a patient with pseudohypoparathyroidism with venous calcification

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• HRP0094P1-20

  A novel TRPM6 variant (c.3179T&#62;A) causing familial hypomagnesemia with secondary hypocalcemia

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• HRP0094P1-21

  Incidence of Type 1 Diabetes in Children and Adolescents during the Covid-19 Pandemic in Germany: Results from the DPV registry

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• HRP0094P1-22

  Early meal reporting enhances post-prandial glycaemic balance but remains underused in teenagers with artificial pancreas

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• HRP0094P1-23

  Capillary blood sample collection at home for HbA1c measurements during the COVID-19 pandemic in children with diabetes mellitus

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• HRP0094P1-24

  Resolution of feeding problems in patients with congenital hyperinsulinism

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• HRP0094P1-25

  Longitudinal Auxological Recovery and Reduced Neurodevelopmental Problems in Hyperinsulinaemic Hypoglycaemia

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• HRP0094P1-26

  Efficacy and Tolerability of GLP-1 Receptor Agonists in Children and Adolescents with Obesity

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• HRP0094P1-27

  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

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• HRP0094P1-28

  Glycemic control and changes in habits in patients with type 1 diabetes during the lockdown due to the COVID-19 pandemic

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• HRP0094P1-29

  Incidence and severity of new-onset paediatric Type 1 diabetes in the COVID-19 pandemic - a UK multicentre perspective

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• HRP0094P1-30

  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

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• HRP0094P1-31

  Efficacy and Safety of Setmelanotide in Individuals With Obesity Due to POMC or LEPR Deficiency: Phase 3 Results From Pivotal and Supplemental Cohorts

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• HRP0094P1-32

  Sex hormones drive changes in lipoprotein profiles in adolescents; early implications for cardiovascular disease risk

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• HRP0094P1-33

  Metabolomics in early life and the association with body composition at age 2 years

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• HRP0094P1-34

  High prevalence of undiagnosed metabolic dysfunction among children and adolescents with obesity in China

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• HRP0094P1-35

  The possible association of the apoptotic marker APO1/Fas with predisposition to metabolic syndrome and mean platelet volume in children

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• HRP0094P1-36

  Reversal of metabolic derangement in patient with congenital generalized lipodystrophy treated with metreleptin

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• HRP0094P1-37

  The effect of trans-palmitoleic acid on lipid accumulation and the fatty acid synthase gene expression in hepatocytes

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• HRP0094P1-38

  Are Serum Spexin Levels Associated With Metabolic Syndrome Antecedents In Obese Adolescents?

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• HRP0094P1-39

  Serum endocan as a predictive biomarker of cardiovascular risk in obese pediatric patients

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• HRP0094P1-40

  Liraglutide for the Management of Childhood Obesity

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• HRP0094P1-41

  Phenotypic Characteristics of Patients with 45,X/46,XY Mosaicism: Growth, Gonadal Pathology and Tumour Risk

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• HRP0094P1-42

  Disorders of sex development: clinical and genetic heterogeneity

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• HRP0094P1-43

  Broad range of phenotypes in an international cohort of 75 DSD individuals with SF-1/NR5A1 variants

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• HRP0094P1-44

  Adolescents and young adult men with non-syndromic hypospadias: testicular function and in-depth genetic screening

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• HRP0094P1-45

  Bilateral testicular regression: genetic etiology and outcome in a large Belgian series

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• HRP0094P1-46

  Endocrine &#38; Molecular Genetic Findings In XY Boys Investigated For A Disorder Of Sex Development: the Glasgow Experience

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• HRP0094P1-47

  <em>STK11</em> gene variant (Peutz-Jeghers Syndrome) presenting with unilateral pre-pubertal gynaecomastia and macro-orchidism without muco-cutaneous pigmentation or gastrointestinal symptoms.

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• HRP0094P1-48

  Gonadal Outcome in 17beta-HSD deficiency and 5alpha-reductase deficiency

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• HRP0094P1-49

  Biallelic <em>PPP2R3C</em> mutations are associated with partial and complete gonadal dysgenesis in 46,XY and 46,XX individuals

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• HRP0094P1-50

  Pathogenic variants in the human m<SUP>6</SUP>A reader YTHDC2 are associated with primary ovarian insufficiency

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• HRP0094P1-51

  A Global Natural History Study (NHS) of Fibrodysplasia Ossificans Progressiva (FOP): Normal Long Bone Growth and Abnormalities in Younger Patients over 36 Months

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• HRP0094P1-52

  Impact of Vertebral Fracture on Auxological Profile and Insulin-like Growth Factors of Children after Acute Lymphoblastic Leukemia Treatment

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• HRP0094P1-53

  Growth and Puberty in Patients with Osteogenesis Imperfecta

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• HRP0094P1-54

  Decreased bone mineral density in children receiving long-term anticoagulation is associated with pubertal development

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• HRP0094P1-55

  Premature epiphyseal fusion induced by a retinoic acid agonist in a young girl with fibrodysplasia ossificans progressiva

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• HRP0094P1-56

  Chondrocyte regulating and other growth plate genes are invaluable growth regulators: a study on children with short stature from 55 consanguineous families

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• HRP0094P1-57

  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

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• HRP0094P1-58

  AAV liver gene therapy-mediated inhibition of FGF23 signaling as a therapeutic strategy for X-linked hypophosphatemia

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• HRP0094P1-59

  Cartilage -specific knockout of SIRT1 significantly reduces bone quality and catch-up growth efficiency

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• HRP0094P1-60

  Mosaic <em>PHEX</em> variants are important causes of X-linked hypophosphataemic rickets.

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• HRP0094P1-61

  Timing of Hypoglycaemia in Patients with Hyperinsulinism (HI): Extension of the Digital Phenotype

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• HRP0094P1-62

  Epidemiology of type 1 diabetes in children and adolescents: a 50-year, single center experience

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• HRP0094P1-63

  Comparison of triglyceride and glucose index and homeostatic model assessment for insulin resistance in children and adolescents with type 2 diabetes mellitus

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• HRP0094P1-64

  Initial Neutrophil/Lymphocyte and Lymphocyte/Monocyte Ratios Can Predict Future Insulin Need in Newly Diagnosed Type 1 Diabetes Mellitus

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• HRP0094P1-65

  Efficacy of Use of Continuous Glucose Monitoring System in patients with Congenital Hyperinsulinism

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• HRP0094P1-66

  Mortality in children with monogenic diabetes

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• HRP0094P1-67

  The Molecular Genetic Etiology by Whole Exome Sequence Analysis in Cases With Familial Type 1 Diabetes Mellitus without HLA Haplotype Predisposition or Incomplete Predisposition

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• HRP0094P1-68

  Birth weight and diazoxide unresponsiveness strongly predict the likelihood of congenital hyperinsulinism due to a mutation in ABCC8 or KCNJ11

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• HRP0094P1-69

  Oxidized lipid-associated protein damage in children and adolescents with type 1 diabetes mellitus: new diagnostic/prognostic clinical markers.

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• HRP0094P1-70

  Change in HbA1C predicts future abnormal Oral Glucose Tolerance Tests in children and adolescents with Cystic Fibrosis.

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• HRP0094P1-71

  Morning salivary cortisol and stress response in term and preterm infants hospitalized in the intensive care unit.

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• HRP0094P1-72

  Clinical characteristics of children with Congenital Hyperinsulinism: Results from the European Registries for Rare Endocrine Conditions (EuRRECa) Project

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• HRP0094P1-73

  Minipuberty in born small for gestational age infants: a case control prospective pilot study

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• HRP0094P1-74

  Pancreatic glucagon-like-peptide-1 receptor expression in congenital hyperinsulinism

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• HRP0094P1-75

  Congenital hyperinsulinism diagnosed after 12 months can have a monogenic aetiology

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• HRP0094P1-76

  Hyperinsulinemic Hypoglycemia in a child with Peroxisomal Biogenesis Disorder due to a Novel PEX1 mutation

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• HRP0094P1-77

  Real-Time Continuous Glucose Monitoring in the Management of Neonates with Persistent Hypoglycemia

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• HRP0094P1-78

  Hyperinsulinemic hypoglycemia due to biallelic mutations in the DNAJC3 gene

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• HRP0094P1-79

  Concurrent hyperinsulinism and hypopituitarism in a 22 month old child due to a novel FOXA2 mutation

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• HRP0094P1-80

  Sphingosine 1- phosphate lyase insufficiency syndrome (SPLIS) as a cause of primary adrenal insufficiency and primary hypogonadism

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• HRP0094P1-81

  Sporadic pituitary adenomas in young patients: clinical and molecular description

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• HRP0094P1-82

  Cardiac remodeling in patients with childhood-onset craniopharyngioma - Results of HIT-Endo and KRANIOPHARYNGEOM 2000/2007

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• HRP0094P1-83

  Pregnancies after childhood craniopharyngioma - Results of Kraniopharyngeom 2000/2007

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• HRP0094P1-84

  Pituitary Duplication - A rare and heterogenous spectrum

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• HRP0094P1-85

  Auxological and endocrine aspects in pediatric patients with type 1 Narcolepsy. Results of long-term follow-up in a pediatric endocrinology center

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• HRP0094P1-86

  Adding a protease inhibitor to sampling tubes increases the acylated ghrelin and decreases the desacylated ghrelin levels in girls.

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• HRP0094P1-87

  GHSR protects the emergence of limited sex differences in anxiety-related behaviors in adult mice after long term THC administration during peri-adolescence

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• HRP0094P1-88

  Pituitary microadenomas in childhood - is follow-up with diagnostic imaging necessary?

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• HRP0094P1-89

  The Pituitary Tumour Module: Developing a Condition Specific Module within the European Registries for Rare Endocrine Conditions (EuRRECa)

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• HRP0094P1-90

  Craniopharyngiomas presenting as incidentalomas: results of KRANIOPHARYNGEOM 2007

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• HRP0094P1-91

  The effect of preoperative calcitriol prophylaxis on post-thyroidectomy hypocalcaemia in children

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• HRP0094P1-92

  Emotional Intelligence scores in children and adolescents with subclinical hypothyroidism - correlation with serum serotonin and thyroid stimulating hormone (TSH) concentrations.

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• HRP0094P1-93

  &#34;Lympocyte population in children and adolescents affected by Graves&#x2019; disease. Potential predictive tool of disease severity&#34;

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• HRP0094P1-94

  Evaluation of children with intrathyroidal ectopic thymus

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• HRP0094P1-95

  Prevalence and Characteristics of thyroid nodules in a pediatric population with congenital hypothyroidism

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• HRP0094P1-96

  Thyroid storm and transient bulbar myopathy in a 22-month-old girl with Graves&#x2019; Disease

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• HRP0094P1-97

  The association between serum Thyrotropin within the reference range and cardiometabolic risk in obese children

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• HRP0094P1-98

  Hypothyroid Screening in Children with Down Syndrome - A Service Evaluation

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• HRP0094P1-99

  Early adiposity rebound in children with congenital hypothyroidism diagnosed by newborn screening

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• HRP0094P1-100

  Serum fibroblast growth factor 21 (FGF-21) levels of children and adolescents with Hashimoto&#x2019;s thyroiditis, before and after L-thyroxin medication

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• HRP0094P1-101

  The management of adrenal cell carcinoma in a single tertiary centre: 25 year experience

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• HRP0094P1-102

  Correlation of 11-oxygenated C19 androgens with the clinical and biochemical characteristics in premature adrenarche

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• HRP0094P1-103

  Leukocyte telomere length in children with Congenital Adrenal Hyperplasia

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• HRP0094P1-104

  [rdquo]Cortison-loop[rdquo] is an educational tool, which helps ensure the quality of care for children with adrenal insufficiency.

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• HRP0094P1-105

  The genetic etiology of ACTH-dependent aldosterone hypersecretion in hypertensive patients without Primary Aldosteronism

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• HRP0094P1-106

  Plasma Proteomics in Healthy Subjects with Differences in Tissue Glucocorticoid Sensitivity Identifies a Novel Proteomic Signature

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• HRP0094P1-107

  Cortoic Acids: Renaissance of a Forgotten Class of Steroids

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• HRP0094P1-108

  Circadian rhythm of cortisol in saliva in obese children with clinical signs of hypercortisolism

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• HRP0094P1-109

  Plasma steroid panel with liquid chromotography-mass spectrometry (LC/MS-MS) method: utilization in differential diagnosis of hyperandrogenism

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• HRP0094P1-110

  Current Management Of Acute Adrenal Insufficiency Related Adverse Events In Children- Results Of An International Survey Of Specialist Centres

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• HRP0094P1-111

  Insulin resistance following childhood craniopharyngioma may influence neural response to food cues in food reward-related brain regions: a preliminary investigation.

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• HRP0094P1-112

  Evaluation of the BigO behavioral indicators in overweight and obese children and adolescents

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• HRP0094P1-113

  Are you considering Idiopathic Intracranial Hypertension when evaluating a patient with obesity?

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• HRP0094P1-114

  EuRRECa Registry Genetic Obesity Survey Results

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• HRP0094P1-115

  Circulating C1q Complement/TNF-Related Protein (CTRP)-13 Levels in Obese Children and Its Relationship with Metabolic Disorders

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• HRP0094P1-116

  An Evidence-based Framework to Evaluate Melanocortin-4 Receptor (MC4R) Pathway Relevance for Obesity-associated Genes

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• HRP0094P1-117

  Serum Fibroblast Growth Factor 23 and Klotho concentrations in children and adolescents with obesity.

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• HRP0094P1-118

  Rare heterozygous variants in genes of the leptin-melanocortin satiety pathway contribute to childhood obesity

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• HRP0094P1-119

  Diagnostic precision of the Tri-Ponderal Mass Index (kg/m<SUP>3</SUP>) to identify the metabolic risk phenotype in obese children and adolescents

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• HRP0094P1-120

  Monogenic obesity in children: focusing on <em>SH2B1</em> deletion

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• HRP0094P1-121

  Higher rates of non-skeletal complications in achondroplasia compared to the general population: a UK matched cohort study using the CPRD database

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• HRP0094P1-122

  Short stature in Protein Arginine Methyltransferase 7 (PRMT7) mutations: first evidences of growth response to rGH treatment

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• HRP0094P1-123

  Growth and nutrition improvement with recombinant growth hormone in prepubertal patients with Silver-Russell syndrome

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• HRP0094P1-124

  Management of endocrine aspects of Noonan syndrome across Europe: A subanalysis of a European clinical practice survey

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• HRP0094P1-125

  PROPEL2: a phase 2, open-label, dose-escalation and dose-expansion study of infigratinib in children with achondroplasia (ACH)

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• HRP0094P1-126

  Identification and tissue-specific characterization of novel SHOX-regulated genes in zebrafish highlights SOX family members among other genes

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• HRP0094P1-127

  Evaluation of early puberty in boys and girls with Silver-Russell Syndrome: Discordance between testicular growth and pituitary-gonadal hormones in male cases

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• HRP0094P1-128

  Evaluation of Persistent Short Stature in Children Born Small for Gestational Age without Catch-up Growth

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• HRP0094P1-129

  Computer-aided facial analysis as a tool to identify patients with Silver-Russell syndrome and Prader-Willi syndrome

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• HRP0094P1-130

  Study design and baseline characteristics of children enrolled in PROPEL: A prospective clinical assessment study in children with achondroplasia (ACH)

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• HRP0094P1-131

  ABSTRACT WITHDRAWN

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• HRP0094P1-132

  Use of growth hormone therapy in short patients born small for gestational age: data from real-life French clinical practice

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• HRP0094P1-133

  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.

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• HRP0094P1-134

  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

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• HRP0094P1-135

  Long-term safety of growth hormone in adults and adolescents with growth hormone deficiency: An overview of the full-cohort in KIMS

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• HRP0094P1-136

  Comparison of actual GH dose with labeled dose in children with short stature based on the LG Growth Study

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• HRP0094P1-137

  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

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• HRP0094P1-138

  Safety and effectiveness of pediatric growth hormone therapy: Results from the full cohort in KIGS

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• HRP0094P1-139

  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

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• HRP0094P1-140

  Linear growth response top Growth hormone therapy in underweight versus normal-weight children with idiopathic short stature (ISS).

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• HRP0094P1-141

  Screening of serum differential proteins in girls with rapidly progressing central precocious puberty with TMT quantitative proteomics

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• HRP0094P1-142

  Investigation of primary adrenal insufficiency (PAI) in children with 46,XY differences in sex development (DSD)

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• HRP0094P1-143

  Current clinical practice of prenatal dexamethasone treatment in at risk pregnancies for classic 21 hydroxylase deficiency in Europe

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• HRP0094P1-144

  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

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• HRP0094P1-145

  Serum anti-Mullerian hormone as a marker of ovarian reserve among childhood cancer survivors

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• HRP0094P1-146

  Reaching a definitive diagnosis of hypogonadotropic hypogonadism - experience of a multidisciplinary diagnostic service

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• HRP0094P1-147

  A pre-analytical challenge to determine estradiol in children: A monovette systematically causing increased estradiol-concentrations in LC-MS/MS analysis

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• HRP0094P1-148

  Central precocious puberty and sleep patterns in COVID-19 outbreak

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• HRP0094P1-149

  QUERY by TELARQUIA: Has there been an increase due to the SARS-COV19 pandemic?

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• HRP0094P1-150

  Androgen insensitivity without an androgen receptor mutation: results from a large cohort study

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• HRP0094P1-151

  Duration of Fasting Studies Required to Demonstrate a Cure for Patients with Focal Congenital Hyperinsulinism.

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• HRP0094P1-152

  Impact of gestational weight gain on methylation of imprinted genes in umbilical cord and its relationship with postnatal growth and metabolism

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• HRP0094P1-153

  Different faces of minipuberty in preterm twin girls

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• HRP0094P1-154

  The Evaluation of Accuracy and Effectiveness of Newborn Screening for Congenital Adrenal Hyperplasia in Lithuania

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• HRP0094P1-155

  Pediatric Inflammatory Multisystemic Syndrome in Brazil: sociodemographic characteristics and risk factors to death

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• HRP0094P1-156

  Molecular and phenotypic profile of Alstrom syndrome in Chinese patients&#xFF1A;results from a Chinese cohort

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• HRP0094P1-157

  Endocrine Monitoring and Outcome After Therapy In Childhood Survivors of Central Nervous System Tumours

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• HRP0094P1-158

  Low adrenal androgen levels in patients with and without primary adrenal insufficiency in APECED (APS1)

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• HRP0094P1-159

  Clinical features and body mineral density in Italian patients with rapid onset obesity with hypoventilation, hypothalamic dysfunction, autonomic disregulation and neural tumor (ROHHADNET): a single center observational study

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• HRP0094P1-160

  Congenital Central Hypothyroidism (CeH) due to a new variant in IGSF1 gene: clinical case of 2 siblings

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• HRP0094P1-161

  Continued Safety and Efficacy of Weekly Lonapegsomatropin (TransCon hGH) for up to Two Years in Children with Growth Hormone Deficiency (GHD)

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• HRP0094P1-162

  Evaluation of growth patterns from the Edinburgh and Gothenburg cohorts by the QEPS model

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• HRP0094P1-163

  The etiology of extreme tall stature above +3 SDS in a screened Finnish population

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• HRP0094P1-164

  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).

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• HRP0094P1-165

  Effects of age of start growth hormone treatment in children with Prader-Willi syndrome: The earlier the better?

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• HRP0094P1-166

  The BoneXpert adult height prediction method outperforms the Bayley and Pinneau method in tall male adolescents.

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• HRP0094P1-167

  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-Registry and rhGH-clinical-trials.

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• HRP0094P1-168

  Mother&#x2019;s smoking during pregnancy influence intrauterine and postnatal growth - the GrowUp 1990 Gothenburg cohort population

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• HRP0094P1-169

  Safety of growth hormone and cardiovascular outcomes in patients with Noonan syndrome enrolled in NordiNet&#174; International Outcome Study (IOS) and the ANSWER Program

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• HRP0094P1-170

  Facilitating Telehealth In A Tertiary Paediatric Endocrine Service: A Quality Improvement Initiative To Reduce The Discrepancy Between Parent-reported And Auxologist Height Measurements

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• HRP0094P1-171

  Diagnosing growth hormone deficiency - Can a combined arginine and clonidine stimulation test replace two separate tests?

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• HRP0094P1-172

  Glucagon Testing of Childhood-Onset Growth Hormone Deficiency during Transition

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• HRP0094P1-173

  Growth hormone receptor 6&ohm; pseudoexon activation: a novel cause of severe growth hormone insensitivity

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  Abstract PDF

• HRP0094P1-174

  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?

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• HRP0094P1-175

  Growth without growth hormone. A tertiary care hospital&#x2019;s experience

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  Abstract PDF

• HRP0094P1-176

  Irisin in the growth hormone deficient children: before and on rhGH therapy.

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  Abstract PDF

• HRP0094P1-177

  Immunogenicity of recombinant growth hormone and relationship its growth-promoting effect in the children with short stature

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• HRP0094P1-178

  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.

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• HRP0094P1-179

  Novel dominant negative GH receptor variants provide important insights into GH receptor physiology

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  Abstract PDF

• HRP0094P1-180

  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

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  Abstract PDF

• HRP0094P1-181

  Continuous versus discontinuous administration of gonadotropin in neonates with congenital hypogonadotropic hypogonadism

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  Abstract PDF

• HRP0094P1-182

  Sequence of MKRN3 and DLK1 genes in cases with familial central precocious puberty

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  Abstract PDF

• HRP0094P1-183

  Hypoandrogenism degree and lipid profile in boys with delayed puberty

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  Abstract PDF

• HRP0094P1-184

  The pituitary gonadal axis is not responsive to GnRH administration in PCSK 1 dysfunction

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  Abstract PDF

• HRP0094P1-185

  Puberty and pituitary-gonadal axis function after treatment for a childhood brain tumor

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• HRP0094P1-186

  Additive effect of androgens and estrogens on pubertal growth acceleration

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  Abstract PDF

• HRP0094P1-187

  The Adrenal Steroid Profile in Adolescent Depression: A Valuable Bio-Readout?

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  Abstract PDF

• HRP0094P1-188

  Congenital hypogonadotropic hypogonadism in a large French cohort : New genetic findings

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  Abstract PDF

• HRP0094P1-189

  Dimensional changes in structures of craniofacial and brain in precocious puberty: Developmental surrogate markers of the brain as a secondary sex characteristic in puberty

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• HRP0094P1-190

  Six novel variants in the MKRN3 gene causing central precocious puberty: characteristics of ten patients and their affected relatives

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  Abstract PDF

• HRP0094P1-191

  The Impact of Hospital Surgical Volume on Healthcare Utilisation Outcomes after Paediatric Thyroidectomy

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  Abstract PDF

• HRP0094P1-192

  Analysis of hypothyroidism NGS test in Korean patients with congenital hypothyroidism in a single center

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  Abstract PDF

• HRP0094P1-193

  Further evidence that Borealin/CDCA8 is involved in thyroid morphogenesis and aging

  Direct

  Abstract PDF

• HRP0094P1-194

  Role of Next Generation Sequencing in the etiological diagnosis of congenital hypothyroidism with gland in situ

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• HRP0094P1-195

  DNA Methylation at a nutritionally sensitive region of the PAX8 gene is associated with thyroid volume and function in Gambian children

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• HRP0094P1-196

  Clinical and Molecular Presentation of Congenital Hypothyroidism Caused by Thyroglobulin Gene Mutations

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  Abstract PDF

• HRP0094P1-197

  Management of newborns born to mothers with autoimmune hypothyroidism

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  Abstract PDF

• HRP0094P1-198

  Novel single nucleotide variation in DUOX2 and NPTX1 genes in two Sardinian sisters with transient congenital hypothyroidism

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  Abstract PDF

• HRP0094P1-199

  New p.Ser237Asn Activating Mutation At The TSHR Receptor, Causing Familial Non- Autoimmune Hyperthyroidism

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• HRP0094P1-200

  Functional studies of <em>PAX8</em> gene variants in patients affected by congenital hypothyroidism with eutopic thyroid gland

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  Abstract PDF

• HRP0094P2-1

  Circadian rhythm of salivary cortisol and cortisone in school-aged children born very preterm and adequate for gestational age

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  Abstract PDF

• HRP0094P2-2

  How do urine steroid metabolites of spot samples correlate with 24 hour urine specimens in children with congenital adrenal hyperplasia?

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  Abstract PDF

• HRP0094P2-3

  Endocrine-disrupting chemicals: an often-forgotten etiology of endocrinological disturbances

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• HRP0094P2-4

  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

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  Abstract PDF

• HRP0094P2-5

  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

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• HRP0094P2-6

  Single centre experience of Hydrocortisone Granules (Alkindi) in children under 6 years of age with Adrenal Insufficiency

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  Abstract PDF

• HRP0094P2-7

  Emotion regulation in congenital adrenal hyperplasia

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• HRP0094P2-8

  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

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  Abstract PDF

• HRP0094P2-9

  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

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  Abstract PDF

• HRP0094P2-10

  Clinical characteristics of cytochrome P450 oxidoreductase deficiency: a nationwide survey in Japan

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  Abstract PDF

• HRP0094P2-11

  Rare Presentation of Adrenal Insufficiency in an Infant with Holocarboxylase Synthetase Deficiency

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• HRP0094P2-12

  Defective Cortisol Secretion in Response to Spontaneous Hypoglycemia but Normal Cortisol Response to ACTH stimulation in neonates with Hyperinsulinemic Hypoglycemia (HH).

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  Abstract PDF

• HRP0094P2-13

  Utilisation Of The I-CAH Registry As A Tool For Facilitating Health Quality Improvement Strategies- Results Of An International Survey Of Specialist Centres

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  Abstract PDF

• HRP0094P2-14

  Clinical and hormonal evolution of aldosterone synthase deficiency: Is complete remission possible?

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  Abstract PDF

• HRP0094P2-15

  Clinical and metabolic characteristics of hyperandrogenic girls with non-classic congenital adrenal hyperplasia and polycystic ovary syndrome

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• HRP0094P2-16

  Rapid clearance of hydrocortisone as a cause of poor control of CAH detected by 24-hour profiling of hydrocortisone concentrations.

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• HRP0094P2-17

  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

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  Abstract PDF

• HRP0094P2-18

  Cushing&#x2019;s disease treatment results correlation with pituitary MRI in children

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• HRP0094P2-19

  Genetic analysis of paediatric primary adrenal insufficiency of unknown aetiology over 25 years

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• HRP0094P2-20

  Panhypopituitarism after treatment procedures in pituitary-hypothalamic area - a single center experience

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• HRP0094P2-21

  The reliability of Salivary Cortisol compared to Serum Cortisol for diagnosing adrenal insufficiency in the gold standard ACTH stimulation test in children

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• HRP0094P2-22

  Prevalence of adrenal insufficiency (AI) requiring treatment with hydrocortisone in children tested with the LDSST

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• HRP0094P2-23

  Serum cortisol and cortisone, and urinary cortisol, cortisone, and tetrahydro-metabolites concentrations in school-aged children born very preterm adequate for gestational age

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• HRP0094P2-24

  The incidence and presentation of congenital adrenal hyperplasia in an unscreened population

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  Abstract PDF

• HRP0094P2-25

  Genotypic Sex and Severity of the Disease Determine the Time of Clinical Presentation in Steroid 17[alpha]-Hydroxylase/17,20-Lyase Deficiency

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• HRP0094P2-26

  Testicular adrenal rest tumour in children with classical congenital adrenal hyperplasia: A case series.

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• HRP0094P2-27

  High doses op&#x2019;-DDD cause metrorragia in young girls

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• HRP0094P2-28

  An Adolescent Case With Adrenoleukodystrophy Diagnosed After Detection Of Leydig Cell Dysfunction

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• HRP0094P2-29

  Fludrocortisone is the salvage treatment in cases with calcineurin inhibitor related hyperkalemia

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• HRP0094P2-30

  Development of a novel weight-based steroid emergency plan for patients with Duchenne Muscular Dystrophy

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• HRP0094P2-31

  Investigation of usage and acceptance of hydrocortisone granules in capsules for opening in children with adrenal insufficiency

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• HRP0094P2-32

  Congenital Adrenal Hyperplasia caused by homozygous pathogenic variant in the HSD3B2 gene.

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• HRP0094P2-33

  Congenital Adrenal Hyperplasia with a <em>CYP21A2</em> deletion overlapping Tenascin-X gene

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• HRP0094P2-34

  Maternal primary adrenal cortex insufficiency during pregnancy: Spotlight on the Fetus and the Neonate. A systematic review and meta-analysis.

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• HRP0094P2-35

  Assessment of blood pressure and carotid intima media thickness (CIMT) in children with primary adrenal insufficiency

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• HRP0094P2-36

  Challenging in diagnosis and treatment of Cushing Disease in a 12 years old boy

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• HRP0094P2-37

  Congenital Adrenal Hyperplasia caused by compound heterozygosity of two novel CYP11B1gene variants.

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• HRP0094P2-38

  Addison&#x2019;s disease: Delay in diagnosis in a girl with longstanding symptoms

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• HRP0094P2-39

  Clinical spectrum of congenital adrenal hyperplasia due to 3 beta hydroxysteroid dehydrogenase deficiency; A case series

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• HRP0094P2-40

  Retrospective Evaluation of Cases Diagnosed with Classical Congenital Adrenal Hyperplasia Due to 21 Hydroxylase Deficiency

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  Abstract PDF

• HRP0094P2-41

  Corticotropin-independent Cushing&#x2019;s Syndrome in toddlerhood: a challenging diagnosis and treatment

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• HRP0094P2-42

  A case of adrenal insufficiency during the course of multisystem inflammatory syndrome in children (MIS-C)

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• HRP0094P2-43

  Aetiology and different clinical conditions of primary adrenal insuffiency in a region of North Africa

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• HRP0094P2-44

  Clinical and evolutionary aspects of Allgrove Syndrome, Algerian experience

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• HRP0094P2-45

  A Rare Coexistence of two autosomal recessive conditions: Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency (CYP21A2 mutation) with Beta Thalassemia Major

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• HRP0094P2-46

  X-linked Adrenoleukodystrophy in south of Tunisia

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• HRP0094P2-47

  Clinical, biological and genetic aspects of congenital adrenal hyperplasia in children at the Central Army Hospital in Algiers

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• HRP0094P2-48

  Coexistence of Adrenal Insufficiency and Hypergonadotropic Hypogonadism: P450scc Deficiency

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  Abstract PDF

• HRP0094P2-49

  Assessment of Patients With Congenital Adrenal Hyperplasia in Armenia

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• HRP0094P2-50

  First case in Lebanon of homozygous mutation in CYP 11B2 leading to isolated aldosterone deficiency.

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  Abstract PDF

• HRP0094P2-51

  A Rare Cause of Hyponatremia in a Child with Hirschsprung Disease Operated with an Ileostomy

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• HRP0094P2-52

  Adrenal insufficiency masquerading as biliary atresia in an infant

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• HRP0094P2-53

  Mutation of NROB1 and Double mutants in cis of CYP21A2 gene in a Chinese boy with primary adrenal insufficiency

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• HRP0094P2-54

  Clinical and hormonal features of the manifestation of various forms of congenital adrenal hyperplasia in children in real clinical practice

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  Abstract PDF

• HRP0094P2-55

  Twin infants with salt-wasting: double the trouble

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  Abstract PDF

• HRP0094P2-56

  Effect of treatment of double precocious puberty in a 9-year-old girl- case report

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• HRP0094P2-57

  Classical Congenital adrenal hyperplasia: about 7 cases

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• HRP0094P2-58

  Denosumab therapy for giant cell granuloma in a paediatric patient: using quantification of Tc99m-MDP uptake on SPECT imaging to guide treatment.

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• HRP0094P2-59

  Vertebral compression and shape in children with osteogenesis imperfecta on regular Zoledronic acid infusions

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• HRP0094P2-60

  Osteosclerotic Metaphyseal Dysplasia: A novel homozygous LRRK1 mutation in two siblings

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• HRP0094P2-61

  Experience of 6-months of burosumab therapy in five siblings with X-linked hypophosphataemic rickets in the State of Kuwait

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• HRP0094P2-62

  Severe Hypophosphatemic Rickets due to Tumor-Induced Osteomalasia

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• HRP0094P2-63

  Diagnostic Challenges of Vitamin D-Dependent Rickets Type 1A (VDDR1A) caused by CYP27B1 mutation in Resource Limited Countries: A Case Series from Three families

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  Abstract PDF

• HRP0094P2-64

  Lack of Cinacalcet response in Neonatal Severe Hyperparathyroidism (NSHPT) due to homozygous CASR mutation

  Direct

  Abstract PDF

• HRP0094P2-65

  Is conventional treatment still the first choice in pediatric patients with PHEX mutations in an era of monoclonal FGF-23 antibody?

  Direct

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• HRP0094P2-66

  Vosoritide Clinical Study Data Demonstrates CXM is a Superior Biomarker of Endochondral Bone Growth

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  Abstract PDF

• HRP0094P2-67

  X-linked hypophosphatemic rickets caused by a large deletion in PHEX gene in a Brazilian family

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• HRP0094P2-68

  Mutational analysis and genotype-phenotype correlation of the PHEX gene in Brazilian patients with X-linked hypophosphatemic rickets

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  Abstract PDF

• HRP0094P2-69

  Evaluation of Admission Characteristics, Treatment and Follow-up Findings of Children with Primary Osteoporosis

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• HRP0094P2-70

  Phenotype characterization of a PHEX intron mutation in an Italian family affected by X linked hypoposphatemic rickets.

  Direct

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• HRP0094P2-71

  Premature epiphyseal fusion induced by Palovarotene in a young girl with fibrodysplasia ossificans progressiva

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• HRP0094P2-72

  ACAN gene skeletal dysplasia (short size syndrome, with or without advanced bone age and early onset osteoarthritis)

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  Abstract PDF

• HRP0094P2-73

  PTEN downregulation in mouse osteoprogenitor cells impacts on bone stability and turnover

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• HRP0094P2-74

  Primary hyperparathyroidism due to a deletion of the CDC73 gene.

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• HRP0094P2-75

  Afebrile seizure in a toddler girl with alopecia: a case report

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• HRP0094P2-76

  A rare cause of hypophosphatemic rickets; Non-lethal Raine syndrome

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• HRP0094P2-77

  Effect of tamoxifen on linear growth of precocious female SD rats

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  Abstract PDF

• HRP0094P2-78

  Deleting STX16 exon 4 to understand the genetic mechanisms underlying pseudohypoparathyroidism-1B and GNAS imprinting

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  Abstract PDF

• HRP0094P2-79

  Clinical, molecular characterization and long-term follow-up of a patient with neonatal severe hyperparathyroidism

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  Abstract PDF

• HRP0094P2-80

  Effect of Soy and Whey on growth pattern in young male Sprague-Dawley rats

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• HRP0094P2-81

  Early-onset osteoporosis due to LRP5

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• HRP0094P2-82

  Vitamin D - What is the Optimal Level in the Pediatric Population

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• HRP0094P2-83

  Schimke immune-osseous dysplasia manifested by stunted growth and spinal epiphyseal dysplasia: a case report

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• HRP0094P2-84

  A rare cause of childhood hypercalcemia: Parathyroid adenoma

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  Abstract PDF

• HRP0094P2-85

  One gene, two diseases: osteogenesis imperfecta, or Bruck syndrome?

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  Abstract PDF

• HRP0094P2-86

  Spontaneous Reshaping of Vertebral Fractures in an Adolescent with Osteogenesis Imperfecta

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  Abstract PDF

• HRP0094P2-87

  A rare presentation of Dysplasia Epiphysealis Hemimelica combined with Familial Hypocalciuric Hypercalcemia - Is this association possible?

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  Abstract PDF

• HRP0094P2-88

  Two sibling cases with heterozygous calcium sensing receptor (CaSR) gene mutation

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  Abstract PDF

• HRP0094P2-89

  Clinical Profile of Parathyroid Adenoma in Children and Adolescents: A single-center experience

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  Abstract PDF

• HRP0094P2-90

  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.

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• HRP0094P2-91

  Two-year experience of burosumab therapy in pediatric XLH patients in Saudi Arabia

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  Abstract PDF

• HRP0094P2-92

  Pseudohypoparathyroidism with hypokalemia and hypomagnesemia: association or separate entity?

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• HRP0094P2-93

  Characterization of Patients with Achondroplasia in a pediatric clinic of Cali, Colombia.

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  Abstract PDF

• HRP0094P2-94

  A Rare Cause of Familial Hypomagnesemia: A Case with Trpm6 Mutation

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• HRP0094P2-95

  Effect of cholecalciferol treatment on serum FGF-23, vitamin D-binding globulin and [alpha]-klotho levels in children with vitamin D deficiency

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  Abstract PDF

• HRP0094P2-96

  HDR Syndrome (Barakat Syndrome): Case Report

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  Abstract PDF

• HRP0094P2-97

  Hungry Bone Syndrome associated to Rickets

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• HRP0094P2-98

  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.

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  Abstract PDF

• HRP0094P2-99

  Glycemic Dysregulation During Treatment Of Childhood Hematologic Malignancies.

  Direct

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• HRP0094P2-100

  The knowledge and Confidence in Management of Diabetic Ketoacidosis (DKA) among Iraqi Paediatric Residents: a Cross Sectional Study

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  Abstract PDF

• HRP0094P2-101

  Disturbances of glucose homeostasis in polytransfused beta-thalassemia patients

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• HRP0094P2-102

  Unmet need in technology for diabetes management in the Middle East, Africa and South East Asia

  Direct

  Abstract PDF

• HRP0094P2-103

  Diabetes in a child with infantile onset multisystem neurological, endocrine and pancreatic disease (IMNEPD)

  Direct

  Abstract PDF

• HRP0094P2-104

  The clinical characteristics of hybrid diabetes (HD) in children and their response to treatment.

  Direct

  Abstract PDF

• HRP0094P2-105

  Recurrent episodes of hypoglycemia in an infant with type 1 spinal muscular atrophy after gene therapy: Beta oxidation defect exaggerated by hepatic dysfunction.

  Direct

  Abstract PDF

• HRP0094P2-106

  Knowledge of the Final Year Medical Students Compared to Interns about the Diagnosis and management of Diabetes Mellitus

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• HRP0094P2-107

  A paradoxical conundrum: diabetic ketoacidosis resulting in treatment-resistant hypokalemic alkalosis

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• HRP0094P2-108

  Impact of the COVID19 pandemic on Paediatric Diabetes Services in Arab Countries

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  Abstract PDF

• HRP0094P2-109

  Clinical Case of Cystic Fibrosis-like and APECED-like Syndrome due to Gain-of-Function Variant in STAT1

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• HRP0094P2-110

  A quality improvement project of a Young Adult Diabetes (YAD) service at a UK specialist centre.

  Direct

  Abstract PDF

• HRP0094P2-111

  Prevalence of skin reactions among pediatrics patients with Type 1 Diabetes users of glucose sensors.

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• HRP0094P2-112

  A single-centre evaluation of remote video consultation for children and young people with diabetes

  Direct

  Abstract PDF

• HRP0094P2-113

  Health Outcome Indicators in Children with Diabetes Mellitus during the SARS-CoV-2 Pandemic

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  Abstract PDF

• HRP0094P2-114

  Evaluation of serum myostatin levels in patients with insulin dependent diabetes mellitus

  Direct

  Abstract PDF

• HRP0094P2-115

  HbA1c and Glucose Management Indicator relationship: can HbA1c determination be avoided?

  Direct

  Abstract PDF

• HRP0094P2-116

  Sex differences over two decades for glycaemic control, pump use and insulin dose in patients aged 10-20 years with type 1 diabetes

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• HRP0094P2-117

  Cardiovascular risk factors in adolescents with type 1 diabetes: Prevalence and gender differences

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• HRP0094P2-118

  Bilateral severe proliferative retinopathy, macular oedema, and lack of macrocytosis in an adolescent male with thiamine-responsive megaloblastic anaemia

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• HRP0094P2-119

  First Survey About Pediatric Diabetes Services in Iraq

  Direct

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• HRP0094P2-120

  Effect of metabolic control on the presence of Nonalcoholic Fatty Liver Disease (NAFLD) in adolescents with type 2 Diabetes.

  Direct

  Abstract PDF

• HRP0094P2-121

  The effect of glycemic variability on DNA damage in pediatric patients with type 1 Diabetes Mellitus

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• HRP0094P2-122

  Parental insulin resistance is associated with unhealthy lifestyle behaviours independently of body mass index in children: The Feel4Diabetes study

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• HRP0094P2-123

  Use of the whole country insulin consumption data in Israel showed a reduced prevalence of type 1 diabetes in children aged &#60;5 years during universal Rotavirus vaccination

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• HRP0094P2-124

  Psychological changes in youth with diabetes: comparison between preadolescents and adolescents

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• HRP0094P2-125

  Focal Congenital Hyperinsulinism in Infancy is Directly Linked to Increased Numbers of Islet Pancreatic Polypeptide Cells in Islets.

  Direct

  Abstract PDF

• HRP0094P2-126

  Oral administration of CRN04777, a nonpeptide selective SST5 receptor agonist, suppresses insulin secretion and rescues hypoglycemia in neonatal rat models of congenital hyperinsulinism

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• HRP0094P2-127

  Thiamine-responsive megaloblastic anemia: a rare presentation of an uncommon disease!

  Direct

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• HRP0094P2-128

  Daily Meal Size Variation Does Not Affect Glycemic Control In T1D Adolescent Patients Equipped With The Closed Loop DBLG1 System

  Direct

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• HRP0094P2-129

  Evaluation of continuous glucose monitoring for the diagnosis of cystic fibrosis related diabetes (CFRD). A prospective and longitudinal study

  Direct

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• HRP0094P2-130

  Blood lipid concentrations of newborns and their mothers with gestational diabetes

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  Abstract PDF

• HRP0094P2-131

  Comparison between hybrid diabetes (HD) and type 2 diabetes (T2DM) in children; Patient&grave;s characteristics at diagnosis: a retrospective observational study.

  Direct

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• HRP0094P2-132

  Features of the manifestation of type 1 diabetes in children in COVID-19 pandemic

  Direct

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• HRP0094P2-133

  Risk factors of autoimmune thyroid disease in children with type 1 diabetes mellitus

  Direct

  Abstract PDF

• HRP0094P2-134

  Does SARS-COV-2 outbreak increase diabetic ketoacidosis in new onset T1DM

  Direct

  Abstract PDF

• HRP0094P2-135

  Heterozygous mutation in the PAX4 gene: a first case description of MODY9 in Vietnam

  Direct

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• HRP0094P2-136

  Evaluation of the Effect of Carbohydrate Count on Nutritional Habits and Metabolic Control in Adolescents with Type 1 Diabetes

  Direct

  Abstract PDF

• HRP0094P2-137

  Nutritional evaluation of children with type 1 diabetes on admission to the Endocrinology-Diabetology and Nutrition Department

  Direct

  Abstract PDF

• HRP0094P2-138

  Correlation between antiinsulin autoantibodies and clinical presentation in T1DM

  Direct

  Abstract PDF

• HRP0094P2-139

  Different schemes of insulin therapy (CSII and MDII) in children with DM1 in a Dnipro city.

  Direct

  Abstract PDF

• HRP0094P2-140

  HbA1c of T1DM Patients before and after Transition - Single Center Experience

  Direct

  Abstract PDF

• HRP0094P2-141

  Glycated Hemoglobin Variability and Microvascular Complications in Patients with Type 1 Diabetes Mellitus

  Direct

  Abstract PDF

• HRP0094P2-142

  Affective response of newly diagnosed Type1 diabetes parents: An experience of a developing country.

  Direct

  Abstract PDF

• HRP0094P2-143

  Short-term glycaemic changes from continuous glucose monitoring among children and adolescents with type 1 diabetes mellitus during fasting in Ramadan month

  Direct

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• HRP0094P2-144

  Is Type 1 Diabetes Mellitus Predictable? Investigation of Predictive Markers n Siblings of Probands with Newly Diagnosed Type 1 Diabetes Mellitus

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  Abstract PDF

• HRP0094P2-145

  Dealing with hypoglycaemia during acute DKA management by paediatric residents from Bahrain, Iraq and Saudi Arabia

  Direct

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• HRP0094P2-146

  A Rare Clinical Case Of A Combination Of Monogenic And Autoimmune Diabetes Mellitus.

  Direct

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• HRP0094P2-147

  Thrombocytopaenia induced by diazoxide treatment in a toddler with Hyperinsulinism-Hyperammonemia syndrome: a rare side-effect

  Direct

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• HRP0094P2-148

  Nephrotic Syndrome and Type 1 Diabetes: a Therapeutic Approach

  Direct

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• HRP0094P2-149

  Assessment of the percentage of T lymphocytes and B lymphocytes with the expression of selected activation markers in patients with type 1 diabetes mellitus depending on the presence of antibodies against EBV antigens.

  Direct

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• HRP0094P2-150

  PIMS-TS [Paediatric Inflammatory Multisystem Syndrome Temporally associated with SARS-CoV-2 (Covid-19)] in a child with new onset type 2 diabetes

  Direct

  Abstract PDF

• HRP0094P2-151

  The impact of COVID-19 lockdown on glycaemic control and BMI in children with type 1 diabetes mellitus (T1DM)

  Direct

  Abstract PDF

• HRP0094P2-152

  Timing of Consulting Paediatric Endocrinologist or Diabetologist During the Management of Acute DKA; Response of Bahraini, Iraqi, and Saudi Paediatric Residents

  Direct

  Abstract PDF

• HRP0094P2-153

  Prevalence and factors associated with microalbuminuria in type 1 diabetic children and adolescents on follow up at Pediatric Endocrinology Clinic in Tikur Anbessa Specialized Hospital, Addis Ababa, Ethiopia

  Direct

  Abstract PDF

• HRP0094P2-154

  Neonatal Diabetes Secondary to Isolated Pancreatic Agenesis

  Direct

  Abstract PDF

• HRP0094P2-155

  Dyslipidaemia in children with type 1 diabetes mellitus

  Direct

  Abstract PDF

• HRP0094P2-156

  The relationship between metabolic parameters atherogenic parameters, atherogenic index and vitamin D levels in children with insulin-dependent diabetes mellitus

  Direct

  Abstract PDF

• HRP0094P2-157

  A case of severe hypertriglyceridaemia complicating new-onset type 1 diabetes mellitus

  Direct

  Abstract PDF

• HRP0094P2-158

  A novel variant HNF1A gene (HNF1A-MODY) in a patient presenting with hyperglycaemia and glycosuria

  Direct

  Abstract PDF

• HRP0094P2-159

  Glucose 6 phosphate dehydrogenase deficiency diagnosed with hemolytic anemia triggered by diabetes mellitus type 1

  Direct

  Abstract PDF

• HRP0094P2-160

  HbA1C stability - is posting samples reliable?

  Direct

  Abstract PDF

• HRP0094P2-161

  Not every obese child has type 2 Diabetes Mellitus

  Direct

  Abstract PDF

• HRP0094P2-162

  Does insulin pump therapy improve glycaemic control in type 1 diabetes children: one year follow up

  Direct

  Abstract PDF

• HRP0094P2-163

  Mauriac syndrome: a complication that still exists in children with type 1 diabetes. Report of a case.

  Direct

  Abstract PDF

• HRP0094P2-164

  The Impact of COVID 19 Pandemic on Type 1 Diabetes Mellitus: An experience of a Tertiary Care Hospital in a resource limited country

  Direct

  Abstract PDF

• HRP0094P2-165

  Co-existence of new onset diabetic ketoacidosis with severe hypertriglyceridemia in a 9 year old girl.

  Direct

  Abstract PDF

• HRP0094P2-166

  How Does Continuous Glucose Monitoring Systems Effect Metabolic Control In Type 1 Diabetes: Single Center Experience

  Direct

  Abstract PDF

• HRP0094P2-167

  Blood level of Vitamin D and metabolic control of type 1 diabetes mellitus

  Direct

  Abstract PDF

• HRP0094P2-168

  Newly-onset type 1 diabetes mellitus triggered by COVID-19: Original case report

  Direct

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• HRP0094P2-169

  Case of HNF1B MODY

  Direct

  Abstract PDF

• HRP0094P2-170

  Diabetes Ketoacidosis Recovery in Youth with Newly Diagnosed and Established Type 1 Diabetes

  Direct

  Abstract PDF

• HRP0094P2-171

  Association of calprotectin with obesity in prepubertal children

  Direct

  Abstract PDF

• HRP0094P2-172

  Metabolic syndrome and birth anthropometric data in Prader-Willi syndrome.

  Direct

  Abstract PDF

• HRP0094P2-173

  Evaluation of the BigO system during the COVID-19 outbreak in Greece

  Direct

  Abstract PDF

• HRP0094P2-174

  The relationship between sleep time and obesity in childhood

  Direct

  Abstract PDF

• HRP0094P2-175

  The relationship between acanthosis nigricans and vitamin D in obese children and adolescents

  Direct

  Abstract PDF

• HRP0094P2-176

  Exploring Urinary Bile Acids as Potential Markers of Metabolism: Reference Values in Children by Targeted LC-MS/MS

  Direct

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• HRP0094P2-177

  A novel mitochondrial tRNA<SUP>Thr</SUP> 15894G&#62;A mutation is potentially risk factor in a Chinese family with obesity

  Direct

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• HRP0094P2-178

  Obesity is potentially associated with a novel mitochondrial tRNA<SUP>Gly</SUP> 10029A&#62;G mutation in a Chinese family

  Direct

  Abstract PDF

• HRP0094P2-179

  Frequency of MC4R Pathway Variants in a Large US Cohort of Pediatric and Adult Patients with Severe Obesity

  Direct

  Abstract PDF

• HRP0094P2-180

  Impact of the COVID-19 pandemic and related lockdown measures on lifestyle behaviours and quality of life in children and adolescents with severe obesity

  Direct

  Abstract PDF

• HRP0094P2-181

  Longitudinal association of the anti-inflammatory serum marker GDF-15 with serum IgA and IgG in apparently healthy children

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• HRP0094P2-182

  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

  Direct

  Abstract PDF

• HRP0094P2-183

  Evaluation of the BigO system in a clinical setting in Greece

  Direct

  Abstract PDF

• HRP0094P2-184

  Assessment of DRD2 dopamine receptor gene rs6277 in pediatric obesity: a case-control study

  Direct

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• HRP0094P2-185

  A Comprehensive, Multidisciplinary, Personalized, Lifestyle Intervention Program is Associated with Increased Leukocyte Telomere Length in Children and Adolescents with Overweight and Obesity

  Direct

  Abstract PDF

• HRP0094P2-186

  Diagnostic accuracy of Tri-Ponderal mass index (kg/m<SUP>3</SUP>) for identifying glucose intolerance in obese children and adolescents.

  Direct

  Abstract PDF

• HRP0094P2-187

  Effect of Semaglutide on body weight in obese children with craniopharyngioma: a preliminary report

  Direct

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• HRP0094P2-188

  Development of a predictive normogram to assess the risk of liver steatosis in childhood obesity

  Direct

  Abstract PDF

• HRP0094P2-189

  Prospective evaluation of liver stiffness in obese children: the role of shear wave elastography.

  Direct

  Abstract PDF

• HRP0094P2-190

  Evaluation of the nutritional behavior of small and large for gestational age children

  Direct

  Abstract PDF

• HRP0094P2-191

  Resting energy expenditure and body composition in children and adolescents with severe obesity due to (suspected) medical causes: comparison between different subtypes of obesity

  Direct

  Abstract PDF

• HRP0094P2-192

  Exercise-induced expression of myokines in adolescents with simple obesity.

  Direct

  Abstract PDF

• HRP0094P2-193

  Early decline in Sertoli cell function during puberty in overweight and obese boys: a cross-sectional study

  Direct

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• HRP0094P2-194

  Vitamin D deficiency in obese children

  Direct

  Abstract PDF

• HRP0094P2-195

  Assessment of Hyperphagia in Patients with Monogenic Obesity

  Direct

  Abstract PDF

• HRP0094P2-196

  Machine Learning Quest for Predictive Markers of Lifestyle Modification Outcomes in Pediatric Obesity Treatment

  Direct

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• HRP0094P2-197

  Triponderal mass index for the categorisation of childhood obesity on the basis of 58.364 observations of 7.792 patients

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• HRP0094P2-198

  Successful weight loss and resolution of hepatic fibrosis in a girl with severe obesity

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• HRP0094P2-199

  Association of Thyroid-Stimulating Hormone and Free Thyroxine Concentrations with Cardiometabolic Risk Factors in Euthyroid Obese Children and Adolescents with Metabolic Syndrome

  Direct

  Abstract PDF

• HRP0094P2-200

  Impact of weight loss on gonadic function in overweight and obese boys

  Direct

  Abstract PDF

• HRP0094P2-201

  Weight status and body composition of children and adolescents during the COVID-19 pandemic

  Direct

  Abstract PDF

• HRP0094P2-202

  The challenges faced in the management of Congenital Generalized Lipodystrophy.

  Direct

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• HRP0094P2-203

  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)

  Direct

  Abstract PDF

• HRP0094P2-204

  Changes in objectively measured physical activity after 2-year lifestyle intervention in pediatric patients with abdominal obesity

  Direct

  Abstract PDF

• HRP0094P2-205

  Assessment of cardiometabolic risk factor clustering in obese children and adolescents with metabolic syndrome

  Direct

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• HRP0094P2-206

  HOMA-IR in obese children with BMI &#8805;2.5SDS, but not &#60;2.5SDS, differ significantly from normal weight children

  Direct

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• HRP0094P2-207

  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

  Direct

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• HRP0094P2-208

  OSAS in childhood obesity is a more frequent and earlier complication than expected

  Direct

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• HRP0094P2-209

  A novel homozygous variant of the leptin receptor (LEPR) gene causing familiar early-onset severe obesity in two siblings

  Direct

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• HRP0094P2-210

  Sleep quality and metabolic syndrome in pediatric patients with abdominal obesity

  Direct

  Abstract PDF

• HRP0094P2-211

  The lockdown effects on a pediatric obese population in the COVID-19 era

  Direct

  Abstract PDF

• HRP0094P2-212

  The Relationship between Acanthosis Nigricans and Vitamin D Levels in Obese Children

  Direct

  Abstract PDF

• HRP0094P2-213

  Influence of birth weight on cardiovascular risk factors in obese children and adolescents

  Direct

  Abstract PDF

• HRP0094P2-214

  A study on the Complications associated with Severe Obesity in Children and Young People

  Direct

  Abstract PDF

• HRP0094P2-215

  The Effectiveness of Indigenous Knowledge-Based Lifestyle Interventions in Preventing Obesity and Type 2 Diabetes Mellitus in Indigenous Children in Canada

  Direct

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• HRP0094P2-216

  The effects of dextroamphetamine treatment in children with hypothalamic obesity

  Direct

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• HRP0094P2-217

  Nutritional status in premature infants born small by gestational age in the first 5 years of life

  Direct

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• HRP0094P2-218

  Impact of overweight and obesity in pediatrics. Metabolic syndrome and its components

  Direct

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• HRP0094P2-219

  What do lipids tell us about the pandemic?

  Direct

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• HRP0094P2-220

  Characteristics of eating behavior in children with type 1 diabetes and obesity

  Direct

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• HRP0094P2-221

  [ldquo]Sleep Properly, Reduce Intake, aNd Get Stepping[rdquo] (SPRINGS): a multidisciplinary approach to managing paediatric morbid obesity with severe obstructive sleep apnoea

  Direct

  Abstract PDF

• HRP0094P2-222

  Design of a Phase 2, Double-Blind, Placebo-Controlled Trial of Setmelanotide in Patients With Genetic Variants in the Melanocortin-4 Receptor Pathway

  Direct

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• HRP0094P2-223

  Absence of dyslipidemia in obese children with BMI &#8805;2.5SDS and similar lipidemic profile to those with BMI &#60;2.5SDS or normal weight

  Direct

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• HRP0094P2-224

  Inflammation associated to body composition in European prepubertal children: Results from the IDEFICS study

  Direct

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• HRP0094P2-225

  A case report of sitosterolemia and the early differential diagnosis

  Direct

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• HRP0094P2-226

  Thyroid function in youth with metabolic syndrome

  Direct

  Abstract PDF

• HRP0094P2-227

  Global survey study of awareness, care and treatment of adolescents living with obesity, their caregivers and healthcare professionals: ACTION Teens

  Direct

  Abstract PDF

• HRP0094P2-228

  Lifestyle habits, consumption of non-nutritive sweeteners and obesity in students and young adults&#x2019; population in Latvia.

  Direct

  Abstract PDF

• HRP0094P2-229

  Influence of the basal metabolic profile on the evolution of the pediatric patient with obesity

  Direct

  Abstract PDF

• HRP0094P2-230

  The utility of continuous glucose monitoring systems in the management of children with persistent hypoglycaemia

  Direct

  Abstract PDF

• HRP0094P2-231

  Hyperinsulinaemic hypoglycaemia as a MEHMO syndrome component: a case report

  Direct

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• HRP0094P2-232

  Methylation of umbilical cord genes associates with gestational weight gain and offspring&#x2019;s cardio-metabolic profile

  Direct

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• HRP0094P2-233

  Diazoxide Responsive Congenital Hyperinsulinism

  Direct

  Abstract PDF

• HRP0094P2-234

  Continuous Glucose Monitoring (CGM) Reveals Undertreated Hypoglycemia in Patients with Congenital Hyperinsulinism

  Direct

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• HRP0094P2-235

  A Selective Nonpeptide Somatostatin Receptor 5 (SST5) Agonist Effectively Decreases Insulin Secretion in a KATPHI Mouse Model and in Human HI Islets

  Direct

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• HRP0094P2-236

  Placental <em>FRAT-1</em> methylation in women with gestational obesity is associated with the body composition in the offspring at 6 years of age

  Direct

  Abstract PDF

• HRP0094P2-237

  Placenta n-6/n-3 PUFA ratio is associated with visceral adiposity and cardiovascular risk in the offspring at 6 years of age

  Direct

  Abstract PDF

• HRP0094P2-238

  Analysis of Placental Steroidogenesis as a Cause of Recurrent Miscarriage

  Direct

  Abstract PDF

• HRP0094P2-239

  Antenatal Markers Related to Fetal Growth Restriction Can Predict Childhood Systolic Blood Pressure

  Direct

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• HRP0094P2-240

  Hypomethylation of the Prader-Willi imprinting control region associates with postnatal growth and visceral adiposity in healthy children

  Direct

  Abstract PDF

• HRP0094P2-241

  Incidence of early neonatal hypoglycemia and some related risk factors in Qatar. A cohort study over two years (2018 and 2019)

  Direct

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• HRP0094P2-242

  Long-term follow-up in a case with congenital hyperinsulinemic hypoglycemia with a novel p.Ser1389Pro mutation in ABCC8 gene

  Direct

  Abstract PDF

• HRP0094P2-243

  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.

  Direct

  Abstract PDF

• HRP0094P2-244

  Genetic Testing Access and Results for Patients with Congenital Hyperinsulinism as Conducted through the CHI and University of Exeter Partnership

  Direct

  Abstract PDF

• HRP0094P2-245

  Predictors of short stature in intrauterine growth retardation in a region of north Africa

  Direct

  Abstract PDF

• HRP0094P2-246

  Massive Open Online Learning - accelerating knowledge in digital health in the management of children with growth disorders

  Direct

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• HRP0094P2-247

  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

  Direct

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• HRP0094P2-248

  Reduction in pappalysin and stanniocalcin levels explain the decrease in IGF-I bioavailability in anorexia nervosa

  Direct

  Abstract PDF

• HRP0094P2-249

  Predictors of short stature in premature infants born small for gestational age

  Direct

  Abstract PDF

• HRP0094P2-250

  Patterns of suboptimal adherence to growth hormone treatment in children living in Italy

  Direct

  Abstract PDF

• HRP0094P2-251

  Screening of celiac disease among children with growth hormone deficiency and idiopathic short stature

  Direct

  Abstract PDF

• HRP0094P2-252

  Pappalysins and stanniocalcins in prenatal and postnatal life

  Direct

  Abstract PDF

• HRP0094P2-253

  GROWPATI Study: Growth and puberty description pattern in a well-characterized cohort of patients with growth retardation due to severe primary IGF1 deficiency

  Direct

  Abstract PDF

• HRP0094P2-254

  Clinic, laboratory and prognostic findings of patients who are diagnosed by Kowarski syndrome (biologically inactive growth hormone)

  Direct

  Abstract PDF

• HRP0094P2-255

  Prevalence of insulin-like growth factor 1 (IGF1) deficiency in prepubertal children with isolated short stature (ISS) and their response to GH therapy.

  Direct

  Abstract PDF

• HRP0094P2-256

  Thyroid function (TF) in short children with idiopathic short stature (ISS) treated with growth hormone (GH)versus those not treated; a controlled study.

  Direct

  Abstract PDF

• HRP0094P2-257

  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

  Direct

  Abstract PDF

• HRP0094P2-258

  Incidence of ALS deficiency in patients with growth hormone deficiency at tertiary pediatric endocrinology center

  Direct

  Abstract PDF

• HRP0094P2-259

  Presentation of IGF-1/IGFBP-3 molar ratio as an effective monitoring index during treatment of growth hormone deficient patients

  Direct

  Abstract PDF

• HRP0094P2-260

  Current growth hormone therapy practices in Belgium for the treatment of short children born small for gestational age

  Direct

  Abstract PDF

• HRP0094P2-261

  Increased height and IGF1 serum levels in children with non-neurofibromatosis type 1 gliomas

  Direct

  Abstract PDF

• HRP0094P2-262

  A Survey on Clinician Perceptions of Long-Acting Growth Hormone Analogs

  Direct

  Abstract PDF

• HRP0094P2-263

  Pituitary gland volume measured by Magnetic Resonance Imaging as diagnostic predictor of persistent Childhood-onset growth hormone deficiency

  Direct

  Abstract PDF

• HRP0094P2-264

  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.

  Direct

  Abstract PDF

• HRP0094P2-265

  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.

  Direct

  Abstract PDF

• HRP0094P2-266

  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.

  Direct

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• HRP0094P2-267

  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.

  Direct

  Abstract PDF

• HRP0094P2-268

  Growth response to growth hormone therapy in short children in relation to their distance from mid-parental heights (MPHt).

  Direct

  Abstract PDF

• HRP0094P2-269

  Immunogenicity of recombinant growth hormone therapy in the children with short stature and consequences on growth-promoting effect

  Direct

  Abstract PDF

• HRP0094P2-270

  Unified training materials to improve adherence to GH-treatment

  Direct

  Abstract PDF

• HRP0094P2-271

  Linear growth of prepubertal children born small for gestational age on growth hormone therapy for 3 years

  Direct

  Abstract PDF

• HRP0094P2-272

  Evaluation of the clinical and laboratory parameters and final adult height in patients treated with recombinant human growth hormone.

  Direct

  Abstract PDF

• HRP0094P2-273

  The results of treatment with growth hormone in a patient with growth hormone deficiency and type 1 diabetes

  Direct

  Abstract PDF

• HRP0094P2-274

  Aetiology and different clinical conditions of GHD in children in a region of North Africa

  Direct

  Abstract PDF

• HRP0094P2-275

  Growth hormone therapy in short stature: The variability of responses to treatment after one year. About 41 cases

  Direct

  Abstract PDF

• HRP0094P2-276

  Growth Hormone Resistance; The Iraqi experience

  Direct

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• HRP0094P2-277

  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

  Direct

  Abstract PDF

• HRP0094P2-278

  Effects of growth hormone therapy on serum concentrations of IGF-1 in patients with Turner syndrome: High IGF-1 concentrations despite optimal dose?

  Direct

  Abstract PDF

• HRP0094P2-279

  The Effect of Hospital Admission and Nutritional Rehabilitation (NR) on Growth and Metabolic abnormalities in adolescent females with severe Anorexia Nervosa (AN)

  Direct

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• HRP0094P2-280

  Outcomes in growth hormone-treated Noonan syndrome children: impact of PTPN11 mutation status

  Direct

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• HRP0094P2-281

  Endocrinological assessment in patients with fanconi anemia

  Direct

  Abstract PDF

• HRP0094P2-282

  Brain-derived neurotrophic factor and matrix metalloproteinases as markers of metabolic status in girls with Turner syndrome.

  Direct

  Abstract PDF

• HRP0094P2-283

  Assessment of genetic defects, baseline characteristics and adverse events reported in the Increlex&#174; registry

  Direct

  Abstract PDF

• HRP0094P2-284

  Associations between height and health-related quality of life (HRQoL) and functional independence in children with achondroplasia

  Direct

  Abstract PDF

• HRP0094P2-285

  COVID 19 impact on Pediatric Endocrinology care - a short story from Romania

  Direct

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• HRP0094P2-286

  Single nucleotide variations associated with short stature in Baka Pygmies as identified by Whole Exome Sequence (WES)

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• HRP0094P2-287

  Novel <em>LZTR1</em> 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 <em>in vitro</em>

  Direct

  Abstract PDF

• HRP0094P2-288

  Comorbidities in Turner Syndrome patients controlled in our center since the 80&#x2019;s

  Direct

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• HRP0094P2-289

  Familial Mosaic Turner Syndrome with short stature and spontaneous puberty due to a ring X chromosome with distal Xp22.3 and distal Xq26 deletion

  Direct

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• HRP0094P2-290

  Linear growth response to growth hormone therapy in underweight versus normal-weight children with idiopathic short stature (ISS)

  Direct

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• HRP0094P2-291

  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 hypoglycemia)

  Direct

  Abstract PDF

• HRP0094P2-292

  Timing of infancy-childhood growth spurt in healthy Turkish children

  Direct

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• HRP0094P2-293

  Effects of GH replacement therapy on body composition and muscle health in children and adolescents with GH deficiency: one-year prospective case-control study.

  Direct

  Abstract PDF

• HRP0094P2-294

  The spectrum of the Prader-Willi-like pheno- and genotype

  Direct

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• HRP0094P2-295

  An Italian survey on GH stimulation tests and their adverse side effects.

  Direct

  Abstract PDF

• HRP0094P2-296

  Comparing the efficacy of nutritional supplementation of different caloric concentrations on linear growth and weight gain in late childhood, a longitudinal study.

  Direct

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• HRP0094P2-297

  The efficacy and safety of recombinant biosimilar growth hormone treatment in children with GHD and SGA: a Czech retrospective national longitudinal study

  Direct

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• HRP0094P2-298

  A qPCR based approach for rapid detection of Turner Syndrome and its variants

  Direct

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• HRP0094P2-299

  Case report: Tall stature, obesity and hip dysplasia in Weaver syndrome due to a loss-of-function variant in <em>EHZ2</em>

  Direct

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• HRP0094P2-300

  Association of Daily Growth Hormone Injection Adherence and Height among Children with Growth Hormone Deficiency

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• HRP0094P2-301

  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.

  Direct

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• HRP0094P2-302

  Two Sibling Cases with Growth Hormone Receptor Mutation: Variable Clinical Expressivity in Laron Syndrome

  Direct

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• HRP0094P2-303

  A literature review of the potency and selectivity of FGFR-selective tyrosine kinase inhibitors, such as infigratinib, in the potential treatment of achondroplasia

  Direct

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• HRP0094P2-304

  Impact of estrogen therapy on pubertal growth in Turner syndrome

  Direct

  Abstract PDF

• HRP0094P2-305

  Anastrozole improves height prediction and near final height as monotherapy or in combination with growth hormone

  Direct

  Abstract PDF

• HRP0094P2-306

  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?

  Direct

  Abstract PDF

• HRP0094P2-307

  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.

  Direct

  Abstract PDF

• HRP0094P2-308

  Evidence that non-syndromic familial tall stature has an oligogenic origin including ciliary genes

  Direct

  Abstract PDF

• HRP0094P2-309

  Early-onset growth hormone treatment in Prader-Willi syndrome attenuates the risk of transition to severe obesity

  Direct

  Abstract PDF

• HRP0094P2-310

  Incidental pituitary adenoma detection in two patients affected by Williams Syndrome: only a coincidence?

  Direct

  Abstract PDF

• HRP0094P2-311

  Efficacy of recombinant growth hormone therapy in TRPS 1 syndrome coexisting with growth hormone deficiency.

  Direct

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• HRP0094P2-312

  Results from the Implementation of a Growth Disorders Related Twinning Programme (Partners4Growth) at tertiary pediatric endocrinology clinics

  Direct

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• HRP0094P2-313

  Co-occurrence of Turner (46,X-ring/45,X0 mosaicism) and Mayer-Rokitansky-Kuster-Hauser Syndromes: a case report

  Direct

  Abstract PDF

• HRP0094P2-314

  Shox Gene Pathologies In Children With Short Stature And Madelung Deformity

  Direct

  Abstract PDF

• HRP0094P2-315

  Characteristics of Patients with Noonan Syndrome Carrying a PTPN11 Mutation: The Recombinant Growth Hormone Treatment and Long-Term Follow-up

  Direct

  Abstract PDF

• HRP0094P2-316

  Determining factors of a good response to treatment with growth hormone for the first 2 years

  Direct

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• HRP0094P2-317

  Noonan syndrome patients with short stature at a single pediatric endocrinology centre

  Direct

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• HRP0094P2-318

  Thyroid status in children with Turner syndrome

  Direct

  Abstract PDF

• HRP0094P2-319

  Rare case report: A Chinese boy with MDPL syndrome cause by <em>POLD1</em> gene mutation

  Direct

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• HRP0094P2-320

  An Unusual Case of Gastrointestinal Bleeding; Expecting the Unexpected

  Direct

  Abstract PDF

• HRP0094P2-321

  Alterations in Metabolic profile and Body Composition in children with Silver Russell syndrome

  Direct

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• HRP0094P2-322

  Growth abnormalities in patients with Type 1 diabetes

  Direct

  Abstract PDF

• HRP0094P2-323

  A novel CEP57 mutation of mosaic variegated aneuploidy syndrome in a Chinese girl: a case report and review of literature

  Direct

  Abstract PDF

• HRP0094P2-324

  A Patient with Turner Syndrome (45X/46XX) and Congenital Adrenal Hyperplasia: A Case Report and Literature Review

  Direct

  Abstract PDF

• HRP0094P2-325

  Impact of oral nutritional supplements on growth outcomes in underweight children (5: 12 years) with no systemic disease.

  Direct

  Abstract PDF

• HRP0094P2-326

  Differential diagnosis of pre- and postnatal short stature revisited: 3-M syndrome

  Direct

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• HRP0094P2-327

  A case of a Floating-Harbor syndrome in a child with severe short stature.

  Direct

  Abstract PDF

• HRP0094P2-328

  Excessive body hair, short stature and advanced bone age in a girl: Hypertrichosis versus adrenarche?

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  Abstract PDF

• HRP0094P2-329

  Cornelia de Lange syndrome: a case report

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  Abstract PDF

• HRP0094P2-330

  Short stature and efficacy of growth hormone treatment in a child with Nail-Patella Syndrome. A case report.

  Direct

  Abstract PDF

• HRP0094P2-331

  Final and Near-final Adult Height and BMI after Long-term Growth Hormone Treatment in Patients with Turner Syndrome (TS)

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  Abstract PDF

• HRP0094P2-332

  Evaluating Safety, Efficacy, and Pharmacokinetics of Weekly TransCon CNP in Children with Achondroplasia: Design of the ACcomplisH Trial

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  Abstract PDF

• HRP0094P2-333

  An Early Diagnosis of Prohormone Convertase Deficiency

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  Abstract PDF

• HRP0094P2-334

  Serologic Testing for Celiac Disease and Gluten Intolerance in a Singaporean paediatric endocrine and growth clinic.

  Direct

  Abstract PDF

• HRP0094P2-335

  Obesity, vaginal bleeding and ovarian mass in a 5-year-old female girl with autoimmune hypothyroidism

  Direct

  Abstract PDF

• HRP0094P2-336

  Endocrine and metabolic complications according to genotype in Prader-Willi syndrome

  Direct

  Abstract PDF

• HRP0094P2-337

  Van Wyk Grumbach Syndrome in an Egyptian Female Pediatric Patient: a rare presentation of a common disease

  Direct

  Abstract PDF

• HRP0094P2-338

  Diagnostic and Follow-up Problems of Medical Care for Prader-Willi Syndrome Children in Resourse-Limited Settings

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  Abstract PDF

• HRP0094P2-339

  Three generations of MEN-1: the importance of family screening

  Direct

  Abstract PDF

• HRP0094P2-340

  Follow-up and management of endocrine and metabolic disorders after hematopoietic stem cell transplantation in a patient followed for Fanconi anemia

  Direct

  Abstract PDF

• HRP0094P2-341

  Neonatal McCune Albright Syndrome Presenting with Diabetes Mellitus

  Direct

  Abstract PDF

• HRP0094P2-342

  Combined pituitary hormone deficiency associated with Graves&#x2019; disease

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  Abstract PDF

• HRP0094P2-343

  Autoimmune polyendocrine syndrome type 2 and precocious puberty: a rare association

  Direct

  Abstract PDF

• HRP0094P2-344

  Thermoregulatory delays in Greek PCOS adolescents

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  Abstract PDF

• HRP0094P2-345

  Endocrine manifestations in familial neurofibromatosis type 1: a case report

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  Abstract PDF

• HRP0094P2-346

  The clinical and biochemical spectrum of pituitary lesions in children compared to adults: experience from a single tertiary center

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  Abstract PDF

• HRP0094P2-347

  Optic tract glioma and endocrine disorders- comparison between patients with and without NF1- a single center experience

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  Abstract PDF

• HRP0094P2-348

  Endocrine manifestations of paediatric intracranial germ cell tumour: from diagnosis to long-term follow-up

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  Abstract PDF

• HRP0094P2-349

  Machine learning to detect the Klinefelter syndrome endocrine profile

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  Abstract PDF

• HRP0094P2-350

  Nuchal Skinfold Thickness in Pediatric Brain Tumor Patients

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  Abstract PDF

• HRP0094P2-351

  Growth hormone deficiency in 52 children with brain Magnetic Resonance Imaging Abnormalities

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  Abstract PDF

• HRP0094P2-352

  Patients with PWS and related syndromes display differentially methylated regions involved in neurodevelopmental and nutritional trajectory.

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  Abstract PDF

• HRP0094P2-353

  Clinical course of primary empty sella in children: a 10-year single-center experience

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  Abstract PDF

• HRP0094P2-354

  Relation between specific pubertal growth and breast maturation - a longitudinal study in healthy girls

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  Abstract PDF

• HRP0094P2-355

  Did Central Precocious Puberty Increase in COVID 19 Pandemic?

  Direct

  Abstract PDF

• HRP0094P2-356

  Delayed diagnosis of paediatric intracranial germ cell tumour (IC-GCTs)

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  Abstract PDF

• HRP0094P2-357

  Gonadotropin-releasing hormone analog treatment in children with idiopathic central precocious puberty: a pharmacovigilance study in a pediatric population.

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  Abstract PDF

• HRP0094P2-358

  Pubertal induction in girls with hypogonadism: preliminary prospective data of efficacy in patients with/without initial overnight estrogen replacement

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  Abstract PDF

• HRP0094P2-359

  Evaluation of pituitary/cranial imaging results of central-puberty precocious cases

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• HRP0094P2-360

  In vivo magnetic resonance spectroscopy as a non-invasive tool for the identification of a sellar tumour in a boy with precocious puberty.

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  Abstract PDF

• HRP0094P2-361

  Rahman Syndrome: Hypopituitarism might be responsible for changing height pattern

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• HRP0094P2-362

  Congenital hypopituitarism: the role of genetics

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  Abstract PDF

• HRP0094P2-363

  Pedigree analysis is essential for clarifying oligogenic transmission in a family with congenital hypogonadotropic hypogonadism (CHH)

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• HRP0094P2-364

  Congenital hypogonadotropic hypogonadism associated with X-linked ichthyosis due to X-chromosome microdeletion identified by chromosomal microarray

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• HRP0094P2-365

  Gonadotropin Flare with Different Depot GnRH Agonists: Comparative Analysis.

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  Abstract PDF

• HRP0094P2-366

  Hypothalamic obesity in children with craniopharyngioma

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  Abstract PDF

• HRP0094P2-367

  Duplication of Pituitary Gland-plus Syndrome presenting with a Transcranial Nasal Dermoid Cyst

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  Abstract PDF

• HRP0094P2-368

  Sterile Abscess Formation with Two Different GnRH Analogues: Three Case Reports

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  Abstract PDF

• HRP0094P2-369

  6-Month GnRHa Formulations Are a Good Choice During the COVID-19 Pandemic and Beyond

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  Abstract PDF

• HRP0094P2-370

  Size Matters: CAG Repeat Length of the Androgen Receptor Gene, Testosterone, and Male Adolescent Depression Severity

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  Abstract PDF

• HRP0094P2-371

  Is quail egg a potential endocrine disruptor?

  Direct

  Abstract PDF

• HRP0094P2-372

  The impact of the Covid-19 pandemic on the UK National Hypothalamic-pituitary Axis Tumour (HPAT) multidisciplinary meeting

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  Abstract PDF

• HRP0094P2-373

  Evaluation of Clinical, Laboratory and Radiological Findings in the Differential Diagnosis of Premature Telarche and Central Puberty Precocious

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  Abstract PDF

• HRP0094P2-374

  Crooke Cell Adenoma as a Rare Cause of Recurrent Cushing Disease: A Challenge in Treatment and Follow-up

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  Abstract PDF

• HRP0094P2-375

  Salivary sex steroids as markers of puberty in boys during late childhood and adolescence

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• HRP0094P2-376

  Efficacy of cabergoline in the treatment of pituitary macroadenoma complicated in a 14-year-old girl.

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• HRP0094P2-377

  Use of Tolvaptan in a child with SIADH post pituitary surgery

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• HRP0094P2-378

  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.

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• HRP0094P2-379

  An Observational, Retrospective Study to Evaluate Long Term Safety and Effectiveness of Leuprorelin in the Treatment of Central Precocious Puberty

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• HRP0094P2-381

  Characterization of puberty development in a large cohort of patients with Noonan syndrome with molecular diagnosis

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  Abstract PDF

• HRP0094P2-382

  Pituitary tumors in children and adolescents: clinical and etiological profile

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  Abstract PDF

• HRP0094P2-383

  Langerhans Cell Histiocytosis with Isolated Central Diabetes Insipidus, Low Grade Fever and Sellar Erosion

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  Abstract PDF

• HRP0094P2-384

  Basal LH as a screening test for diagnosis of central precocious puberty

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  Abstract PDF

• HRP0094P2-385

  A Practical Method for the Evaluation of Childhood Hypophysitis: Pituitary Stalk/Basilary Artery Ratio

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  Abstract PDF

• HRP0094P2-386

  Blood Pressure in Girls with Central Precocious Puberty and GnRH Analog Therapy

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  Abstract PDF

• HRP0094P2-387

  Isolated central diabetes insipidus and periventricular nodular heterotopia in a 9-year-old girl

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  Abstract PDF

• HRP0094P2-388

  Central precocious puberty: clinical, etiologic and therapeutic features

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  Abstract PDF

• HRP0094P2-389

  Atypical Presentation of Pituitary Macroadenoma in an adolescent girl: Central Hypothyroidism and Attenuated Pubertal Growth Spurt.

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  Abstract PDF

• HRP0094P2-390

  A case of partially Empty Sella with hypopituitarism in a child

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  Abstract PDF

• HRP0094P2-391

  Cushing&#x2019;s disease in paediatric patients: Diagnosis and evolution

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  Abstract PDF

• HRP0094P2-392

  Late Puberty In Children

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  Abstract PDF

• HRP0094P2-393

  First Morning Voided Urinary Gonadotropin Measurements for the Early Screening, Diagnosis and Follow-up of Central Precocious Puberty Patients

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  Abstract PDF

• HRP0094P2-394

  SRY negative 46XX male syndrome: case report

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  Abstract PDF

• HRP0094P2-395

  Cognitive function and linear growth in Prednisone-treated children with salt-wasting congenital adrenal hyperplasia

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  Abstract PDF

• HRP0094P2-396

  Combining big data science with clinics: Novel approach for understanding human sex development and its variants.

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  Abstract PDF

• HRP0094P2-397

  Vascular dysfunction and increased cardiovascular risk in hypospadias

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  Abstract PDF

• HRP0094P2-398

  Evaluation of genomic copy number variations in the etiology of syndromic patients with diferences of sex development (DSD)

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  Abstract PDF

• HRP0094P2-399

  Self-reported Feelings of Adult Patients with Differences of Sex Development (DSD) Regarding Genital Surgical Procedures

  Direct

  Abstract PDF

• HRP0094P2-400

  Peripheral Precocious Puberty in girls affected by McCune-Albright Syndrome: safety and efficacy retrospective study on letrozole treatment

  Direct

  Abstract PDF

• HRP0094P2-401

  Two sisters with primary hypergonadotrophic hypogonadism, pubertal progress and deletion of 61.5MB of &#x3A7;q21.33q28 region

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  Abstract PDF

• HRP0094P2-402

  Description of a new variant in the MAMLD1 gene in an infant with microphallus and hypospadias

  Direct

  Abstract PDF

• HRP0094P2-403

  Surgical aspects of the multicentric and interdisciplinary study in minors with different sexual development

  Direct

  Abstract PDF

• HRP0094P2-404

  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

  Direct

  Abstract PDF

• HRP0094P2-405

  Serum high mobility group box 1 (HMGB1) levels are independently associated with glucose clamp-derived measures of insulin resistance in PCOS

  Direct

  Abstract PDF

• HRP0094P2-406

  <em>ZSWIM7</em> is associated with human female meiosis and familial primary ovarian insufficiency

  Direct

  Abstract PDF

• HRP0094P2-407

  Is the recommended dual therapy for transsexual boys harmless?

  Direct

  Abstract PDF

• HRP0094P2-408

  Plexiform neurofibroma of the penis as an infrequent manifestation debut in a pediatric patient

  Direct

  Abstract PDF

• HRP0094P2-409

  Surprising X Chromosomes: Unusual Mosaicism

  Direct

  Abstract PDF

• HRP0094P2-410

  Puberty delay in girls: etiological structure of the disease

  Direct

  Abstract PDF

• HRP0094P2-411

  Rationale for a reduced dexamethasone dose in prenatal congenital adrenal hyperplasia therapy based on pharmacokinetic modelling

  Direct

  Abstract PDF

• HRP0094P2-412

  45,X/46,XY mosaicism: Phenotypic characteristics, growth, and gonadal features

  Direct

  Abstract PDF

• HRP0094P2-413

  Challenges faced by children and adolescents with Differences in Sex Development (DSD) managed at a tertiary care specialized university center in Sri Lanka

  Direct

  Abstract PDF

• HRP0094P2-414

  A novel mutation of SOX2 gene in an idiopathic hypogonadotropic hypogonadism patient with olfactory bulb agenesis

  Direct

  Abstract PDF

• HRP0094P2-415

  Obesity, ovarian mass, vaginal bleeding and hypothyroidism in a 5-year-old female girl

  Direct

  Abstract PDF

• HRP0094P2-416

  Ovarian Juvenile Granulosa Cell Tumor in 9-Month-Old female Infant presented with Isosexual Pseudo Puberty: Case Report

  Direct

  Abstract PDF

• HRP0094P2-417

  A case report of Non-syndromic 46, XX testicular DSD presenting as a genital ambiguity - Clinical, molecular and cytogenetic analysis

  Direct

  Abstract PDF

• HRP0094P2-418

  46 XX, SRY negative testicular DSD presenting with VACTERL Syndrome

  Direct

  Abstract PDF

• HRP0094P2-419

  A late revelation of Sexual differentiation disorder 46XX due to 11 beta hydroxylase deficiency

  Direct

  Abstract PDF

• HRP0094P2-420

  Gonadal tumor risk, bone mineral density, and genetics, clinical, hormonal, and psychosexual aspects of a large androgen insensitivity syndrome cohort

  Direct

  Abstract PDF

• HRP0094P2-421

  Radiological evaluation of children with atypical genitalia due to disorders of sex development (46, XY DSD) in a resource-limited setup

  Direct

  Abstract PDF

• HRP0094P2-422

  17-hydroxylase deficiency and diabetes in a case with 46 XY female

  Direct

  Abstract PDF

• HRP0094P2-423

  Diagnostic dilemma in a patient with central precocious puberty: Ovarian steroid cell tumor

  Direct

  Abstract PDF

• HRP0094P2-424

  Dimensional approach to gender dysphoria in nigeria: Association with socio-demographics and psycho-sexual variables

  Direct

  Abstract PDF

• HRP0094P2-425

  Puberty delay in girls: Analyses of disease structure depending on clinical characteristics

  Direct

  Abstract PDF

• HRP0094P2-426

  Uterus agenesia in a patient with CATCH 22 Syndrome. Purpose of a case

  Direct

  Abstract PDF

• HRP0094P2-427

  High throughput screening of DSD candidate genes with the help of the powerful model <em>Drosophila melanogaster</em>

  Direct

  Abstract PDF

• HRP0094P2-428

  Case series: Use of tamoxifen in the management of gynaecomastia in three adolescent boys with 46 XY DSD

  Direct

  Abstract PDF

• HRP0094P2-429

  4-year-old female patient with mixed germ cell tumor and underlying Cowden syndrome

  Direct

  Abstract PDF

• HRP0094P2-430

  A comparison between Androstanolone and Testosterone Enanthate for penile augmentation in patients with idiopathic micropenis

  Direct

  Abstract PDF

• HRP0094P2-431

  Combination therapy of hypogonadotropic hypogonadism with rFSH and hCG &#x2013; case report

  Direct

  Abstract PDF

• HRP0094P2-432

  46,XY DSD due to biallelic DHX37 gene mutations

  Direct

  Abstract PDF

• HRP0094P2-433

  Novel mutation in an iranian family with 17-&#x3B2; hydroxysteroid dehydrogenase type 3 deficiency

  Direct

  Abstract PDF

• HRP0094P2-434

  A case of gender developmental disorder with difficulty in molecular diagnosis: New variant in NR5A1 gene

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  Abstract PDF

• HRP0094P2-435

  Two pedigrees with congenital bilateral anorchia in one sibling and testicular torsion at adolescence in another: a shared genetic predisposition?

  Direct

  Abstract PDF

• HRP0094P2-436

  Importance of testicular biopsy for validation of diagnosis; cryptorchidism, analyzing prescrotal undescended testes

  Direct

  Abstract PDF

• HRP0094P2-437

  Rare genetic disorder associated with microphallus

  Direct

  Abstract PDF

• HRP0094P2-438

  Congenital adrenal hyperplasia in detail: A multicentric and interdisciplinary study in minors with different sexual development

  Direct

  Abstract PDF

• HRP0094P2-439

  Sex assignment at birth: is it always easy?

  Direct

  Abstract PDF

• HRP0094P2-440

  Combination therapy of hypogonadotropic hypogonadism in boys with rFSH and hCG &#x2013; case reports analyses

  Direct

  Abstract PDF

• HRP0094P2-441

  Clinical case of premature ovarian failure in combination with blepharophimosis-ptosis-epicanthus inversus due to mutation in <em>FOXL2</em> gene

  Direct

  Abstract PDF

• HRP0094P2-442

  Persistent M&#xFC;llerian duct syndrome presenting with bilateral cryptorchidism and obstructed inguinal hernia

  Direct

  Abstract PDF

• HRP0094P2-443

  5 alpha-reductase type 2 deficiency: A case report

  Direct

  Abstract PDF

• HRP0094P2-444

  An unexplained cause of unilateral gynecomastia in a 3-year-old boy

  Direct

  Abstract PDF

• HRP0094P2-445

  Could intramuscular testosterone differentiate between partial androgen insensitivity and 5 alpha reductase type 2 deficiency?

  Direct

  Abstract PDF

• HRP0094P2-446

  The efficacy and short- and long-term side effects of radioactive iodine treatment in pediatric Graves&#x2019; disease: a systematic review

  Direct

  Abstract PDF

• HRP0094P2-447

  Incidentally detected papillary thyroid cancer with elevated calcitonin in a 15 year-old female: A case report

  Direct

  Abstract PDF

• HRP0094P2-448

  Methimazole-induced remission rates in pediatric graves&#x2019; disease: A systematic review

  Direct

  Abstract PDF

• HRP0094P2-449

  Congenital multinodular goiter causing acute airway obstruction in a newborn: a case report

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  Abstract PDF

• HRP0094P2-450

  Initial response to thionamide medication in young people with newly diagnosed thyrotoxicosis

  Direct

  Abstract PDF

• HRP0094P2-451

  A girl with Trisomy 21 presents with Van Wyk-Grumbach syndrome. A rare diagnosis

  Direct

  Abstract PDF

• HRP0094P2-452

  Complications after pediatric thyroidectomy: lymph node dissection is a risk factor for permanent hypocalcemia

  Direct

  Abstract PDF

• HRP0094P2-453

  Kinetics of FT4 serum concentrations in newborns and infants with congenital hypothyroidism during follow-up differ in the three severity groups

  Direct

  Abstract PDF

• HRP0094P2-454

  Thyroid dysfunction in small for gestational age infants: a need for second screening?

  Direct

  Abstract PDF

• HRP0094P2-455

  Expression of Zinc transporter 8 in thyroid tissues from patient with immune and non-immune thyroid diseases

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  Abstract PDF

• HRP0094P2-456

  Hashimoto Thyroiditis: long term follow-up from childhood to young adulthood

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• HRP0094P2-457

  A case of complete atrioventricular block after initiation of methimazole in a patient with Graves&#x27; disease associated with Down&#x27;s syndrome previously undergoing cardiac surgery

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  Abstract PDF

• HRP0094P2-458

  Unilateral autoimmune ophthalmopathy as a first symptom in manifestation of autoimmune thyroiditis and systemic lupus erythematosus in an adolescent girl. Case report.

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  Abstract PDF

• HRP0094P2-459

  Incidence and etiology of primary congenital hypothyroidism in Flanders

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  Abstract PDF

• HRP0094P2-460

  Re-evaluation of the prevalence of permanent congenital hypothyroidism in Niigata, Japan: A retrospective study

  Direct

  Abstract PDF

• HRP0094P2-461

  Early reassessment in congenital hypothyroidism

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  Abstract PDF

• HRP0094P2-462

  Growth impairment in children with severe autoimmune primary hypothyroidism and pituitary hyperplasia without goiter

  Direct

  Abstract PDF

• HRP0094P2-463

  The Use Of Intravenous Introduction Of Glucocorticoids In The Active Stage Of Graves&#x2019; Ophthalmopathy In Childhood. Clinical Case

  Direct

  Abstract PDF

• HRP0094P2-464

  Atypical presentation of acute suppurative thyroiditis in a 6 year old child

  Direct

  Abstract PDF

• HRP0094P2-465

  Allan-Herndon-Dudley syndrome: case report of a rare disorder

  Direct

  Abstract PDF

• HRP0094P2-466

  Direct

  Abstract PDF

• HRP0094P2-467

  Direct

  Abstract PDF

• HRP0094P2-468

  Thyroid function in preterm infants admitted to the neonatal intensive care unit: a single center study

  Direct

  Abstract PDF

• HRP0094P2-469

  Thyroid dysfunction in Beta-thalassemia patients

  Direct

  Abstract PDF

• HRP0094P2-470

  Victim pathologies of the pandemic. Severe acquired hypothyroidism

  Direct

  Abstract PDF

• HRP0094P2-471

  Mitigating thyroid cancer risk in multinodular hyperplasia secondary to a 10q23.31 deletion (PTEN Hamartoma Tumour Syndrome)

  Direct

  Abstract PDF

• HRP0094P2-472

  Thyroid dysfunction and autoimmune thyroiditis in children with new-onset diabetes mellitus

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  Abstract PDF

• HRP0094P2-473

  A rare cause of congenital hypothyroidism: Brain-lung-thyroid syndrome

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• HRP0094P2-474

  Recurrent fractures in a child with Graves&#x27; disease

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• HRP0094P2-475

  Case study of 13- year-old boy suffering from papillary thyroid cancer in stage pT3aN1bMX

  Direct

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• HRP0094P2-476

  Evaluation of general characteristics of children with hypothyroidism

  Direct

  Abstract PDF

• HRP0094P2-477

  L-T4 absorption test in 14-year-old patient with severe refractory hypothyroidism after total thyroidectomy

  Direct

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• HRP0094P2-478

  A child with anti-thyroid arthritis syndrome

  Direct

  Abstract PDF

• HRP0094P2-479

  Thyroglobulin deficiency: a rare cause of neonatal stridor

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  Abstract PDF

• HRP0094P2-480

  TBG deficiency and Central Congenital Hypothyroidism (CCH): Our experience in neonatal screening with TSH and T4

  Direct

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• HRP0094P2-481

  A case of hypothyroidism post bone marrow transplantation

  Direct

  Abstract PDF

• HRP0094P2-482

  Iodine status and autoimmune thyroiditis in children; a case-control study in Sri Lanka

  Direct

  Abstract PDF

• HRP0094P2-483

  A 9-year-old girl with Van Wyk and Grumbach syndrome: precocious puberty as a rare consequence of hypothyroidism

  Direct

  Abstract PDF

• HRP0094P2-484

  Iodine Deficiency Cretinism in Tuva Republic

  Direct

  Abstract PDF

• HRP0094P2-485

  Prevalence and associated factors of Congenital Hypothyroidism in Bogot&#xE1;, Colombia. 2014 - 2020

  Direct

  Abstract PDF

• HRP0094P2-486

  Aetiology and different clinical condition of hypothyroidism in children and adolescents

  Direct

  Abstract PDF

• HRP0094P2-487

  Influenza A induced Thyrotoxic Storm Post Haematopoietic Stem Cell Transplantation

  Direct

  Abstract PDF

• HRP0094P2-488

  The state of iodine deficiency in Krasnoyarsk territory according to results of neonatal TSH screening in 2019

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  Abstract PDF

• HRP0094P2-489

  Thyrotropic cell hyperplasia secondary to prolonged uncontrolled primary hypothyroidism

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• HRP0094P2-490

  Thyroid dyshormonogenesis: a case report of two siblings with a heterozygous variant in the TPO gene.

  Direct

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• HRP0094P2-491

  Pediatric Graves&#x2019; disease in southern Tunisia

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