autosomal dominant nonsyndromic deafness 15

An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset with high frequency progressive hearing loss and has_material_basis_in mutation in the POU4F3 gene on chromosome 5q32.

Signs and symptoms

• Hearing impairment

Also known as: DFNA15; DFNA52; autosomal dominant deafness 15; autosomal dominant deafness 52; autosomal dominant nonsyndromic deafness 52