autosomal recessive nonsyndromic deafness 25

An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with moderate to profound, progressive hearing loss and has_material_basis_in mutation in the GRXCR1 gene on chromosome 4p13.

Signs and symptoms

• Hearing impairment
• Progressive sensorineural hearing impairment
• Abnormal vestibular function

Also known as: DFNB25; autosomal recessive deafness 25