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Autosomal Recessive Nonsyndromic Deafness 39
An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, downsloping hearing loss and is caused by mutation in the HGF gene on chromosome 7q21.
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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, downsloping hearing loss and is caused by mutation in the HGF gene on chromosome 7q21.
Resources
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