autosomal recessive nonsyndromic deafness 24

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 RDX gene on chromosome 11q22.

Signs and symptoms

• Profound sensorineural hearing impairment

Also known as: DFNB24; autosomal recessive deafness 24