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Charcot-Marie-Tooth Disease Type 2A2B
A Charcot-Marie-Tooth disease type 2 characterized by onset of peripheral neuropathy in the first years of life that is caused by homozygous or compound heterozygous mutation in the MFN2 gene on chromosome 1p36.22.
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When to seek help
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Overview
A Charcot-Marie-Tooth disease type 2 characterized by onset of peripheral neuropathy in the first years of life that is caused by homozygous or compound heterozygous mutation in the MFN2 gene on chromosome 1p36.22.
Resources
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Posts in this community reflect personal experiences, not medical advice. Always talk to your doctor before changing your treatment.