autosomal recessive nonsyndromic deafness 79

An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, stable hearing loss and has_material_basis_in mutation in the TPRN gene on chromosome 9q34.

Signs and symptoms

• Delayed speech and language development
• Progressive sensorineural hearing impairment
• Sensorineural hearing impairment

Also known as: DFNB79; autosomal recessive deafness 79