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Autosomal Recessive Nonsyndromic Deafness 77
An autosomal recessive nonsyndromic deafness that is characterized by postlingual onset with moderate to profound, progressive hearing loss and is caused by mutation in the LOXHD1 gene on chromosome 18q21.
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When to seek help
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Overview
An autosomal recessive nonsyndromic deafness that is characterized by postlingual onset with moderate to profound, progressive hearing loss and is caused by mutation in the LOXHD1 gene on chromosome 18q21.
Resources
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