hrp0092p2-198 | Growth and Syndromes (to include Turner Syndrome) | ESPE2019

Evaluation of Diagnosis, Follow-up and Treatment Results of Growth Hormone in Rare Diseases; 10 Year Single Center Experience

Aycan Zehra , Arasli Yilmaz Aslihan , Yel Servet , Savas Erdeve Senay , Çetinkaya Semra

Introduction: Growth hormone therapy (GHT); have been used in rare diseases such as growth hormone deficiency (GHD), panhipopituitarism (PHP), intrauterine growth retardation (IUGR), Turner Syndrome(TS) for many years while the effects of diagnostic timing on the treatment results are known. However,data on the diagnosis and treatment processes of these diseases are limited in our country. The aim of this study was to evaluate the results of diagnosis, follow-...

hrp0098p3-216 | Pituitary, Neuroendocrinology and Puberty | ESPE2024

A Case of Adipsic Diabetes Insipidus with Craniopharyngioma

Korkmaz Vural Meltem , Karacan Küçükali Gülin , Sarıkaya Özdemir Behiye , Yel Servet , Aslı Bala Keziban , Keskin Meliksah , Kurnaz Erdal , Savas Erdeve Senay

Introduction: Adipsic diabetes insipidus (ADI) arises from the destruction of both antidiuretic hormone (ADH) neurons and osmoreceptors in the hypothalamus. This condition is characterized by polyuria, loss of thirst sensation and hypernatremia. Managing serum sodium levels is particularly challenging, often resulting in fluctuations in serum sodium and osmolality, which elevate the risk of morbidity and mortality. This report presents the clinical follow-up o...

hrp0098p3-242 | Sex Differentiation, Gonads and Gynaecology, and Sex Endocrinology | ESPE2024

Efficacy of Letrozole in Managing Prepubertal Gynecomastia Associated with Peutz-Jeghers Syndrome: A Case Study

Yel Servet , Bora Ulukapi Hasan , Kurnaz Erdal , Keskin Meliksah , Asli Bala Keziban , Ozbay Hosnut Ferda , Dere Gunal Yasemin , Gokce Cinar Hasibe , Savas Erdeve Senay

Introduction: Peutz-Jeghers syndrome (PJS) is a disorder characterized by autosomal dominant inheritance, hamartomatous polyps in the gastrointestinal system, mucocutaneous pigmentation, and a predisposition to malignancies, caused by mutations in the STK11 gene. In male patients, large cell calcifying Sertoli cell tumors associated with prepubertal gynecomastia can be observed. We present a case of prepubertal gynecomastia that led to a diagnosis of PJS durin...