autosomal dominant nonsyndromic deafness 82

An autosomal dominant nonsyndromic deafness characterized by onset of rapidly progressive bilateral sensorineural hearing loss usually early in the first decade that has_material_basis_in heterozygous mutation in the ATP2B2 gene on chromosome 3p25.1.

Signs and symptoms

• Sensorineural hearing impairment
• Tinnitus

Also known as: DFNA82; autosomal dominant deafness 82