autosomal dominant nonsyndromic deafness 10

An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset in the third or forth decade of life with a flat or gently downsloping audioprofiles and has_material_basis_in mutation in the EYA4 gene on chromosome 6q23.

Signs and symptoms

• Sensorineural hearing impairment

Also known as: DFNA10; autosomal dominant deafness 10