autosomal dominant nonsyndromic deafness 23

An autosomal dominant nonsyndromic deafness that is characterized by prelingual onset with high frequency progressive hearing loss and has_material_basis_in mutation in the SIX1 gene on chromosome 14q23.

Signs and symptoms

• Conductive hearing impairment
• Vesicoureteral reflux
• Sensorineural hearing impairment
• Preauricular pit

Also known as: DFNA23; autosomal dominant deafness 23