Wednesday, June 20, 2018

Usher syndrome

usher syndrome -

Usher syndrome is a rare genetic disease caused by mutations in one of the ten genes, causing hearing loss and visual impairment (and being one of the causes of deafness). Currently Usher syndrome is still not cured.

Other names of Usher syndrome are Hallgren syndrome, Usher-Hallgren syndrome, retinitis pigmentosa-disaciusis syndrome, and retinal dysphagia distrophia syndrome.