autosomal recessive nonsyndromic deafness 32

An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, stable hearing loss and male infertility in some affected men that has_material_basis_in mutation in the CDC14A gene on chromosome 1p21.2.

Signs and symptoms

• Sensorineural hearing impairment
• Abnormal sperm morphology
• Male infertility
• Immotile sperm

Also known as: DFNB32; HIIMS; autosomal recessive deafness 105; autosomal recessive deafness 32; hearing impairment infertile male syndrome