hrp0097fc4.5 | Growth and syndromes (to include Turner syndrome) | ESPE2023

From thalidomide embryopathy to genetic defects of the upper limb, internal organs, cerebral midline, and pituitary: The phenotypic spectrum of SALL4

Kodytková Aneta , Anne Amaratunga Shenali , Zemková Daniela , Maratová Klára , Dušátková Petra , Plachý Lukáš , Průhová Štěpánka , Koloušková Stanislava , Lebl Jan

Introduction: In 1950s - 1960s, the thalidomide disaster resulted in congenital malformations in more than 10,000 children. Derivative of thalidomide interferes with early embryonic transcriptional regulation due to selective degradation of SALL4 protein and thus, thalidomide embryopathy phenocopies pathogenic variants of the SALL4 gene. Their phenotypes range from phocomelia, reduced radial ray, to defects of the heart, kidneys, eye, and cerebral mid...

hrp0097p2-288 | Late Breaking | ESPE2023

Validation of utility of a single LH measurement 40 minutes after depot Leuprolide acetate 3.75 mg and 11.25 mg in assessing gonadotropic activity in girls with CPP: Comparison with a standard GnRH stimulation test at diagnosis and during treatment.

Helvacıoğlu Didem , Demircioğlu Serap , Güran Tülay , Haliloğlu Belma , Türkmen Nilsu , Gurpınar Tosun Buşra , Kahveci Ahmet , Bereket Abdullah

Context: Intravenous Gonadotropin-Releasing-Hormone (GnRH) stimulation test has a central role in evaluating gonadotropic activation in the diagnosis and monitorization of the treatment in patients with central precocious puberty (CPP). However, this test is invasive, laborious, costly and availability of GnRH preparation is limited in some countries.Objective: To evaluate the utility of the LH level measured 40-minutes ...

hrp0098p1-32 | Diabetes and Insulin 2 | ESPE2024

Factors Associated with Pump Set Occlusion

Tuğçe Tunca Küçükali Elif , Kuşkanadı Büşra , Özdemir Uslu Zülal , Akın Agâh , Muratoğlu Şahin Nursel , Çetinkaya Semra

Introduction: The most common non-metabolic complication of insulin pump therapy is set occlusion, and the literature on factors associated with occlusion is limited. This study aims to investigate the factors influencing set occlusion.Methods: A total of 52 patients with type 1 diabetes using insulin pumps were included in the study. A 36-item questionnaire related to set occlusion was administered to the healthcare per...

hrp0098p2-282 | Thyroid | ESPE2024

Thyroid hormone profile and autoimmunity in down syndrome

Günay Aylin , Helvacıoğlu Didem , Yavaş Abalı Zehra , Gürpınar Tosun Büşra , Kahveci Ahmet , Kurt İlknur , Keleştemur Elif , Tuğba Canbaz Aylin , Haliloğlu Belma , Güran Tülay , Bereket Abdullah , Turan Serap

Down syndrome (DS) is the most common chromosomal disorder in live births (1/1500-1/700) and caused by a meiotic nondisjunction (trisomy 21). DS is associated with an increased risk of thyroid disorders in addition to other systemic problems. In this study, we aim ed to investigate the thyroid hormone profiles and associated autoimmune diseases in DS.Material and Method: DS patients, aged 0-18 years, who were followed for thyroid problem...