hrp0098p1-103 | Thyroid 1 | ESPE2024

The Relationship Between Antiepileptic Drug Use and Central and Peripheral Thyroid Hormone Sensitivity

Ali Oktay Mehmet , Tuğçe Tunca Küçükali Elif , Döğer Esra , Arhan Ebru , Demir Ercan , Orhun Çamurdan Mahmut , Bideci Aysun

Introduction: There is a complex and multifaceted relationship between antiepileptic drugs (AEDs) and the neuroendocrine system. Thyroid hormone (TH) sensitivity reflects thyroid homeostasis more comprehensively than serum hormone levels. It is clear whether TH sensitivity is associated with the use of AEDs. In this study, the evaluation of thyroid hormone sensitivity is aimed in euthyroid cases treated with antiepileptic drug therapy. In this study, the evalu...

hrp0098p2-107 | Fat, Metabolism and Obesity | ESPE2024

Xq27.3-q28 Duplication Containing FMR1 Gene: Case Presentation and Literature Review of Familial X-linked Hypogonadism, Gynecomastia, Short Stature, Intellectual Disability and Obesity Syndrome

Ali Oktay Mehmet , Tuğçe Tunca Küçükali Elif , Kayhan Gülsüm , Döğer Esra , Orhun Çamurdan Mahmut , Bideci Aysun

Introduction: Syndromic obesities are characterized by malformations, dysmorphic features, and/or neurodevelopmental disorders. This paper reports the clinical characterization of a duplication showing familial transmission in the Xq27.3q28 region containing the FMR1 gene, presenting symptoms such as obesity, hypogonadism, gynecomastia, short stature, and intellectual disability.Case Presentation: A 17-year-old male pati...

hrp0098p2-179 | Growth and Syndromes | ESPE2024

An Uncommon Cause of Short Stature: 18q Deletion

Tuğçe Tunca Küçükali Elif , Ali Oktay Mehmet , Kayhan Gülsüm , Döğer Esra , Orhun Çamurdan Mahmut , Bideci Aysun

Introduction: 18q deletion is one of the rare causes of short stature, characterized by intellectual disability, short stature, hypotonia, hearing loss, and foot deformities. Patients with this condition are also found to have an increased susceptibility to autoimmune diseases, which can lead to associated endocrinopathies. Here, we present a case diagnosed with 18q deletion and followed in our clinic due to short stature.Case:</...

hrp0098p2-253 | Sex Differentiation, Gonads and Gynaecology, and Sex Endocrinology | ESPE2024

A Rarely Detected Variant in 46,XX Disorders of Sex Development: Recurrent p.Arg92Trp Variant in NR5A1

Ali Oktay Mehmet , Akın Agah , Döğer Esra , Kayhan Gülsüm , Eşme Kocaman Gizem , Orhun Çamurdan Mahmut , Bideci Aysun

Introduction: 46,XX testis/ovotesticular (OT) disorders of sex development (DSD) are rare conditions where gonadal differentiation in 46,XX individuals leads towards testicular development. SRY-negative 46,XX OT-DSD is even rarer compared to other DSDs.Case Presentation: A male patient presented at the age of 3 due to micropenis. Physical examination revealed penile hypospadias and bifid scrotum; phallus length was 2.2 c...

hrp0098p3-139 | GH and IGFs | ESPE2024

Growth Hormone Therapy in Congenital Tufting Enteropathy: A Case Report and Literature Review

Ali Oktay Mehmet , Orhun Çamurdan Mahmut , Eğritaş Gürkan Ödül , Alan Tehçi Başak , Döğer Esra , Bideci Aysun

Introduction: Congenital tufting enteropathy (CTE) is a rare autosomal recessive enteropathy that typically presents in early life and is often characterized by persistent diarrhea. Height standard deviation scores (SDS) and body mass indexes are generally low in patients with CTE. However, information about the effects of growth hormone (GH) therapy in these patients is lacking.Case Presentation: A 13-year-old girl with...