autosomal recessive nonsyndromic deafness 59

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 DFNB59 gene on chromosome 2q31.

Signs and symptoms

• Sensorineural hearing impairment

Also known as: DFNB59; autosomal recessive deafness 59