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ey0020.10-9 | Metabolic Syndrome | ESPEYB20

10.9. The association of metabolic syndrome status with sensorineural hearing loss in pediatric obese patients

O Ozdemir , A Ucar , AD Cakir , E Misir , O Yigit

Brief summary: This study assessed the relation between the metabolic syndrome (MetS) and sensorineural hearing loss in children with obesity. Children with MetS were shown to have subclinical hearing loss compared to those without MetS.Comment: Associations between obesity and hearing loss have been reported in several adult studies.1 However, similar studies in adolescents have yielded conflicting results. The present study aimed to address ...

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ey0021.13-9 | Endocrinology | ESPEYB21

13.9. 17α Hydroxylase/17,20 lyase deficiency: clinical features and genetic insights from a large Turkey cohort

Z Siklar , E Camtosun , S Bolu , M Yildiz , A Akinci , F Bas , İ Dundar , A Bestas , E Unal , P Kocaay , T Guran , G Buyukyilmaz , AK Ugurlu , BG Tosun , I Turan , E Kurnaz , B Yuksel , D Turkkahraman , A Cayir , G Celmeli , EN Gonc , BS Eklioğlu , S Cetinkaya , SK Yilmaz , ME Atabek , M Buyukinan , E Arslan , E Mengen , EDP Cakir , M Karaoglan , N Hatipoglu , Z Orbak , A Ucar , N Akyurek , ED Akbas , E Isik , SB Kaygusuz , ZK Sutcu , G Seymen , M Berberoglu

Brief Summary: This retrospective cohort study analyzed data from 97 cases of 17α hydroxylase/17,20 lyase deficiency identified in Turkey. It focused on diagnostic testing, laboratory characteristics, long-term outcomes and therapeutic management.This nationwide study focuses on 17α-Hydroxylase/17,20-Lyase deficiency (17OHD), a rare form of congenital adrenal hyperplasia (CAH) caused by mutations in the CYP17A1 gene. The research aims to evalua...

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ESPE Yearbook of Paediatric Endocrinology

10.9. The association of metabolic syndrome status with sensorineural hearing loss in pediatric obese patients

13.9. 17α Hydroxylase/17,20 lyase deficiency: clinical features and genetic insights from a large Turkey cohort

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