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Autosomal Dominant Nonsyndromic Deafness 20
An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset with high frequency progressive hearing loss and is caused by mutation in the ACTG1 gene on chromosome 17q25.
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When to seek help
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Overview
An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset with high frequency progressive hearing loss and is caused by mutation in the ACTG1 gene on chromosome 17q25.
Resources
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Posts in this community reflect personal experiences, not medical advice. Always talk to your doctor before changing your treatment.