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Autosomal Recessive Nonsyndromic Deafness 110
An autosomal recessive nonsyndromic deafness characterized by prelingual, bilateral hearing loss that is caused by homozygous or compound heterozygous mutation in the COCH gene on chromosome 14q12.
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When to seek help
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Overview
An autosomal recessive nonsyndromic deafness characterized by prelingual, bilateral hearing loss that is caused by homozygous or compound heterozygous mutation in the COCH gene on chromosome 14q12.
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Posts in this community reflect personal experiences, not medical advice. Always talk to your doctor before changing your treatment.