autosomal dominant nonsyndromic deafness 11

An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset in the first decade of life with a flat or gently downsloping audioprofiles and has_material_basis_in mutation in the MYO7A gene on chromosome 11q13.

Signs and symptoms

• Bilateral sensorineural hearing impairment
• Abnormal vestibular function
• Vertigo

Also known as: DFNA11; autosomal dominant deafness 11