Wolfram-like syndrome autosomal dominant

Wolfram-like syndrome autosomal dominant

A condition (OMIM:614296) characterised by the clinical triad of congenital progressive hearing impairment (of low- and middle-frequency ranges, with onset in the first decade of life), diabetes mellitus and optic atrophy.
Molecular pathology
Defects of WFS1, which encodes a transmembrane protein that regulates Ca2+ homeostasis, cause Wolfram-like syndrome autosomal dominant.