autosomal recessive nonsyndromic deafness 28

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 TRIOBP gene on chromosome 22q13.

Signs and symptoms

• Severe sensorineural hearing impairment

Also known as: DFNB28; autosomal recessive deafness 28