Searchable abstracts of presentations at key conferences in endocrinology

ea0035p638 | Female reproduction | ECE2014

Wolfram syndrome with hypergonadotropic hypogonadism: case report

Sahin Murat , Oguz Ayten , Yilmaz Selda , Inanc Elif , Ozdemir Murat , Yilmaz Mehmet Alparslan , Gul Kamile

Introduction: Wolfram syndrome has characterized by central diabetes insipidus (DI), diabetes mellitus (DM), optic atrophy (OA) and deafness. In this report we presented a Wolfram syndrome with hypergonadotropic hypogonadism.Case: A 18-year-old girl who has diabetes for 6 years was hospitalized due to blood sugar irregularity. Her medical history revealed frequent urination and enuresis for 2–3 years and primary amenorrhea. Furthermore she had hear ...