Searchable abstracts of presentations at key conferences in endocrinology

ea0026p630 | Clinical case reports | ECE2011

A rare variant of Wolfram syndrome with diabetic microvascular disease, hypergonadotropic hypogonadism and palmar fibromatosis: case report

Preda C , Gaspar I , Ungureanu M-C , Leustean L , Cristea C , Moisii L , Mogos V , Vulpoi C

Introduction: Wolfram syndrome, a very rare condition, is a neurodegenerative disorder characterized by diabetes insipidus, diabetes mellitus, optic atrophy and deafness (DIDMOAD) which appear in childhood, hampering diagnosis and treatment. Others less frequent features as hypergonadotropic hypogonadism, microvascular disease and local fibromatosis are reported in a male patient diagnosed at the age of 18 years.Case report: An 18-year-old male patient d...