autosomal dominant nonsyndromic deafness 44

An autosomal dominant nonsyndromic deafness that is characterized postlingual onset with low to mild frequency progressive hearing loss and has_material_basis_in mutation in the CCDC50 gene on chromosome 3q28.

Signs and symptoms

• Sensorineural hearing impairment
• Abnormal vestibular function
• Tinnitus
• Abnormal inner ear morphology

Also known as: DFNA44; autosomal dominant deafness 44