ea0037ep1265 | Clinical Cases–Thyroid/Other | ECE2015
Ozdemir Didem
, Polat Sefika Burcak
, Bestepe Nagihan
, Ozbek Saliha
, Ersoy Reyhan
, Cakir Bekir
Introduction: Leri–Weill dyschondrosteosis (LWD) is a rare autosomal dominant dyschondrosteosis characterised by Madelung deformity and mesomelic dwarfism. Majority of cases are associated with haploinsufficiency of the short-stature homeobox-containing (SHOX) gene. Here we report a patient with LWD and diabetes mellitus (DM).Case report: A 31 years old man applied with polyuria and polydipsia. He did not have any chronic disease. In family history,...