autosomal dominant nonsyndromic deafness 28

An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset with flat or gently downsloping audioprofiles and has_material_basis_in mutation in the GRHL2 gene on chromosome 8q22.

Signs and symptoms

• Sensorineural hearing impairment

Also known as: DFNA28; autosomal dominant deafness 28