autosomal recessive nonsyndromic deafness 77

An autosomal recessive nonsyndromic deafness that is characterized by postlingual onset with moderate to profound, progressive hearing loss and has_material_basis_in mutation in the LOXHD1 gene on chromosome 18q21.

Signs and symptoms

• Bilateral sensorineural hearing impairment
• Abnormal vestibular function
• Tinnitus

Also known as: DFNB77; autosomal recessive deafness 77