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Autosomal Recessive Nonsyndromic Deafness 22
An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, stable hearing loss and is caused by mutation in the OTOA gene on chromosome 16p12.
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When to seek help
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Overview
An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, stable hearing loss and is caused by mutation in the OTOA gene on chromosome 16p12.
Resources
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Posts in this community reflect personal experiences, not medical advice. Always talk to your doctor before changing your treatment.