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Autosomal Dominant Nonsyndromic Deafness 12
An autosomal dominant nonsyndromic deafness that is characterized by prelingual onset and mid-frequency hearing loss and is caused by mutation in the TECTA gene on chromosome 11q23.
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When to seek help
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Overview
An autosomal dominant nonsyndromic deafness that is characterized by prelingual onset and mid-frequency hearing loss and is caused by mutation in the TECTA gene on chromosome 11q23.
Resources
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Posts in this community reflect personal experiences, not medical advice. Always talk to your doctor before changing your treatment.