autosomal dominant nonsyndromic deafness 20

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 ACTG1 gene on chromosome 17q25.

Signs and symptoms

• Bilateral sensorineural hearing impairment
• Progressive sensorineural hearing impairment

Also known as: DFNA20; DFNA26; autosomal dominant deafness 20