hrp0084p3-1167 | Puberty | ESPE2015

In a Severe Precocious Puberty Case Who Treated with Frequent Leuprolid Acetate Injections, a Rare Adverse Effect: Sterile Abscess

Keskin Mehmet , Karaoglan Murat , Demir Korcan , Keskin Ozlem

Introduction: GnRH analogues common used in precocious puberty are highly effective agents. The drug dose and injection frequency should be designed for each case. However these agents are common well tolerated, some rare adverse effects may be occur. We present a case of frequent leuprolid acetate injections-related sterile abscess.Case: The case was 16-month-old boy. He had rapid growth, big penis, and excessive pubic hair. These symptoms have appeared...

hrp0084p3-1192 | Thyroid | ESPE2015

The Comparing of Thyroid Volumes between Healthy and Obese Children in Respect of Anthropometric, Biochemical, and Metabolic Parameters

Keskin Mehmet , Karaoglan Murat , Balci Onur , Ozkur Ayhan , Keskin Ozlem

Objective: There have no been studies enough about thyroid volumes of obese and adolescent children. In this study, we purposed comparing of thyroid volumes in respect of anthropometric, biochemical, metabolic parameters in following groups: Overweight, obese, morbid obese, and healthy children.Method: Two groups were compared: The first group consisted of 190 children whose BMIs are above the 85th percentile. The second group was 90 children with normal...

hrp0084p3-1219 | Thyroid | ESPE2015

Unilateral Graves’ Disease in an Adolescent: Case Report

Eklioglu Beray Selver , Atabek Mehmet Emre , Akyurek Nesibe , Tastekin Gungor

Background: GravesÂ’ disease is a rare autoimmune thyroid disease that characterized by hyperthyroidism, diffuse goitre and ophthalmopathy. It generally involved both lobes of the thyroid, unilateral involvement was rare.Case report: A 18 year old girl presented with weakness, alopecia, menstruel irregularity. In physical examination moist skin, increased pulse rate (116/min) and enlargement of the right lobe of the thyroid was determined. Her blood ...

hrp0094p2-476 | Thyroid | ESPE2021

Evaluation of general characteristics of children with hypothyroidism

Bulut Eman , Eklioglu Beray Selver , Atabek Mehmet Emre

Aim: This study aimed to investigate retrospectively the demographic, clinical and laboratory data of patients followed up for hypothyroidism and to determine the insidance of persistent hypothyroidism.Materials and Methods: A total of 209 patients with hypothyroidism were included retrospectively in this study. Demographic data, clinical features, laboratory results, thyroid volume, follow-up time, treatment drug were recorded. These patients were divid...

hrp0094p2-156 | Diabetes and insulin | ESPE2021

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

Zenger Gulberil , Selver Eklioglu Beray , Emre Atabek Mehmet , Kurban Sevil ,

Objective: Vitamin D plays an important role in hyperlipidemia, cardiovascular disease risk, and glucose/insulin metabolism. The aim of this study is; to investigate the relationship between serum vitamin D levels and metabolic profiles of children with T1DM, atherogenic index, and cardiovascular disease risk.Materials and Methods: T1DM patients were included in the study retrospectively. Anthropometric and clinical measurements, biochem...

hrp0094p2-212 | Fat, metabolism and obesity | ESPE2021

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

Daye Munise , Selver Eklioglu Beray , Atabek Mehmet Emre ,

Aim: Acanthosis nigricans (AN) is the most important skin complication of obesity. In our study, the relationship of acanthosis nigricans and vitamin D levels was evaluated in children.Methods: Obese children aged between 6 and 18 years old, who were examined in the pediatric endocrinology outpatient clinic, were included. The patientsÂ’ anthropometric measurements and laboratory results and vitamin D levels were rec...

hrp0097p1-30 | Bone, Growth Plate and Mineral Metabolism | ESPE2023

A Novel Stop Codon Mutation in Exon 6 (c.508A>T) of TRAPPC2 gene in a Patient with X-Linked Spondyloepiphyseal Dysplasia Tarda: A Case Report

Yaşar Deniz , Güleray Lafcı Naz , Karacan Küçükali Gülin , Araslı Yılmaz Aslıhan , Özkaya Dönmez Beyhan , Tahir Yazar Burak , Uçan Berna , Okur İclal , Sarıkaya Özdemir Behiye , Kurnaz Erdal , Keskin Melikşah , Savaş Erdeve Şenay

Spondyloepiphyseal dysplasia tarda (SEDT) is an inherited disorder that is diagnosed in childhood or adolescence presents with disproportionate short stature and premature osteoarthritis with frequently affecting men. Here, we described a novel nonsense mutation, c.508A>T; p.Lys170Ter, in TRAPPC2 in a Turkish patient with X-linked SEDT. The patient is a 15-year-old boy from Turkish non-consanguineous parents, presented decreasing height velocity last three years and also th...

hrp0095p1-437 | Diabetes and Insulin | ESPE2022

The Relationship between Visceral Adipose Index and Metabolic Syndrome in Children with Type 1 Diabetes Mellitus

Albayrak Serpil , Karaoglan Murat , Keskin Mehmet , Yıldırım Ahmet

Background/Aim: Prediction of metabolic syndrome (Mets) plays important role in cardiovascular disease risk prevention. Although Mets is relatively common in children with T1DM, diagnosis and prediction are ignored. Visceral Adiposity Index VAI) has been defined as a new cardiometabolic risk marker reflecting abdominal fat distribution and dyslipidemia. The aim of the study is to reveal the relationship between Mets and components of VAI in patients with T1DM....

hrp0095p2-303 | Late Breaking | ESPE2022

Donohue syndrome in a Turkish infant: Mild clinical course despite severe genetic mutation

Tepe Derya , Kocaay Pinar , Cakir Gundogan Secil , Sirma Dokuzboy Refika , Boyraz Mehmet

Donohue syndrome(DS) is a rare and often lethal autosomal recessive disease. Its prevalence is estimated less than one in a million live births. Mutations in the insulin reseptor (INSR) gene cause rare severe INSR-related insulin resistance syndromes such as DS. It is characterized by severe insulin resistance (hyperinsulinemia, fasting hypoglycemia and postprandial hyperglycemia), intrauterine and postnatal growth retardation, hypotonia, organomegaly including heart, liver, k...

hrp0092rfc8.1 | Pituitary, Neuroendocrinology and Puberty Session 1 | ESPE2019

Trade-Off Between Olfactory Bulb and Eyeball Volume in Precocious Puberty

Karaoglan Murat , Colakoglu Er Hale , Aytaç Kaplan Emel , Keskin Mehmet

Context: Olfactory bulb (OB) and eyeball size change depending on age and puberty. There is well-established trade-off between sensory structures of brain such as eye and olfactory bulb.Objective: The aim of this study is to analyze the potential reciprocal changes between OB and eyeball volumes (EV) in girls with precocious puberty (PP), as a sign of early pubertal onset.Design: A...