autosomal recessive nonsyndromic deafness 94

An autosomal recessive nonsyndromic deafness characterized by prelingual profound sensorineural hearing loss that has_material_basis_in homozygous or compound heterozygous mutation in the NARS2 gene on chromosome 11q14.1.

Signs and symptoms

• Bilateral sensorineural hearing impairment
• Abnormal vestibular function

Also known as: DFNB94; autosomal recessive deafness 94