ESPE Abstracts

ESPE Abstracts

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60th Annual ESPE (ESPE 2022)

Rome, Italy
15 Sept 2022 - 17 Sept 2022

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The 60th ESPE Annual Meeting will now be taking place in Rome, Italy.

Poster Category 1

Thyroid

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Sex Differentiation, Gonads and Gynaecology, and Sex Endocrinology
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Late Breaking

hrp0095p1-187 | Thyroid

Analysis of miR-15a-5p, miR-126-3p, miR-142-5p and miR-150-5p levels in blood of children and adolescents with thyroid diseases

hrp0095p1-188 | Thyroid

A case report of Hirschsprung Disease and C Cell Hyperplasia: a new RET gene variant?

hrp0095p1-189 | Thyroid

Resistance to Thyroid Hormone β in an infant with a novel de novo mutation of the THRB gene

hrp0095p1-190 | Thyroid

Genetic spectrum of 26 Korean patients with congenital hypothyroidism by targeted next-generation sequencing

hrp0095p1-191 | Thyroid

Hyperthyroidism leading to Idiopathic Intracranial Hypertension in a Child – A Case Report

hrp0095p1-192 | Thyroid

Hashimoto’s Encephalopathy in children: a case report

hrp0095p1-193 | Thyroid

Diagnostic Features and Risk Factors for Childhood Thyroid Cancers

hrp0095p1-194 | Thyroid

Response to initial treatment in a pediatric cohort of patients with papillary thyroid cancer (PTC): changes after 3 years of follow up

hrp0095p1-195 | Thyroid

Molecular Characterisation of Patients with Thyroid Dyshormonogenesis and Variants in DUOX2

hrp0095p1-196 | Thyroid

Diffuse Sclerosing Variant of Papillary Thyroid Cancer in a boy with Goldenhar Syndrome

hrp0095p1-197 | Thyroid

A familial case of PAX8 gene variant with incomplete penetrance

hrp0095p1-198 | Thyroid

FT3:FT4 ratio be used to predict relapse and remission? Single Centre Experience

hrp0095p1-199 | Thyroid

Thyroid Hormone Receptor Resistance Alpha: Case Report

hrp0095p1-200 | Thyroid

Severe and Non Severe Forms of Autoimmune Hypothyroidism in Childhood: A Retrospective Analysis of 256 Cases

hrp0095p1-386 | Thyroid

Relationships of urinary bisphenol A in childhood on thyroid hormone function in adolescents

hrp0095p1-387 | Thyroid

Pediatric Graves Disease (PGD): presentation, treatment and follow up. A single center Argentine perspective

hrp0095p1-388 | Thyroid

Next Generation Sequencing Analysis of Congenital Hypothyroidism Patients in A Single Tertiary Center

hrp0095p1-389 | Thyroid

Increasing incidence of Pediatric Graves’ Disease

hrp0095p1-390 | Thyroid

Does serum thyroglobulin predict thyroxine requirement during infancy in athyreosis and thyroid ectopia?

hrp0095p1-391 | Thyroid

Biochemical Indicators of Euthyroid Sick Syndrome in Critically Ill Children

hrp0095p1-392 | Thyroid

Clinical Features, Risk Classifications and Long-Term Follow Up Of Childhood Differentiated Thyroid Cancer(DTC): A Single Reference-Center Experience

hrp0095p1-393 | Thyroid

Urinary Iodine Concentration and Thyroid Function in Children by Age

hrp0095p1-394 | Thyroid

Analysis on the influencing factors of neonatal serum FT3, FT4 and TSH

hrp0095p1-395 | Thyroid

Liquid formulations of Levothyroxine with and without ethanol in the treatment of congenital hypothyroidism: similar TSH and fT4 values in the first six months of follow up

hrp0095p1-396 | Thyroid

A rare cause of acquired von Willebrand factor deficiency: Primary hypothyroidism due to autoimmune thyroiditis

hrp0095p1-397 | Thyroid

Molecular Diagnosis of Non-Autoinmune Subclinical Hypothyroidism in Paediatrics

hrp0095p1-398 | Thyroid

Unusually Enlarged Ovaries Associated with Severe Hypothyroidism - Van Wyk and Grumbach Syndrome Case Report

hrp0095p1-399 | Thyroid

Evaluation of Childhood Thyroid Nodules: A Single Center Experience

hrp0095p1-400 | Thyroid

Total thyroidectomies for endocrinologic indication: Experience in a third level hospital

hrp0095p1-586 | Thyroid

Newborn screening for congenital hypothyroidism through dried blood spot in Low middle income country (LMIC):experience from a tertiary care center

hrp0095p1-587 | Thyroid

Sensitivity to Thyroid Hormones and Metabolic Syndrome in Pediatric Patients with Neuromotor Disability

hrp0095p1-588 | Thyroid

Thyrotoxicosis in children and adolescence in Iceland: A twenty-year retrospective study

hrp0095p1-589 | Thyroid

Familial Dysalbuminemic Hyperthyroxinemia (FDH) in Asymptomatic Child with High Free T4 and Normal TSH

hrp0095p1-590 | Thyroid

Immunoglobulin Superfamily 1 (IGSF1) Deficiency: A Rare Cause of Isolated Congenital Hypothyroidism in Two Siblings

hrp0095p1-591 | Thyroid

Evaluation of Permanent and Transient Congenital Hypothyroidism in Cases Referred from National Neonatal Screening Program

hrp0095p1-592 | Thyroid

Development of delayed thyrotropin elevation in small-for-gestational-age infants: Is a second screening needed?

hrp0095p1-593 | Thyroid

Genetic and Functional Studies of Patients with Thyroid Dyshormonogenesis Associated with Defects in The TSH Receptor (TSHR)

hrp0095p1-594 | Thyroid

Unexpected fast growth velocity in a child with a thyroid hormone receptor beta mutation

hrp0095p1-595 | Thyroid

Treatment of Graves' Disease in Children and adolecents with Long-Term Antithyroid Drugs: A 20-Year Single-Center Experience

hrp0095p1-596 | Thyroid

Central and peripheral sensitivity to thyroid hormones and glucose metabolism in childhood obesity.

hrp0095p1-597 | Thyroid

Congenital hypothyroidism: outcome of a 26 year screening (1996-2021)

hrp0095p1-598 | Thyroid

Retrospective analysis and literature review of five cases of thyroid hormone resistance syndrome caused by THRB gene mutation

hrp0095p1-599 | Thyroid

Twin pregnancy with a hydatiform mole and coexisting liveborn infant, with maternal hyperthyroidism and neonatal hypothyroidism

hrp0095p1-600 | Thyroid

Response to Growth Hormone Therapy in Turner And Noonan Syndrome: First Year And Final Height

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