[Hearing loss due to mutations in the genes responsible for Usher syndrome].

Abstract excerpt

Usher syndrome is characterized by congenital bilateral sensorineural hearing loss and progressive retinitis pigmentosa, and has an autosomal recessive type of inheritance. The purpose of this work is to summarize the modern data of a clinical picture of Usher syndrome and analyse hearing impairment properties. The frequency of the syndrome among children suffering from hearing loss and deafness is from 3 to 10%....

Topics

Share this publication in a Topic to start or enrich a Post.

• Share to Child
• Share to Hearing Tests
• Share to Mutation