Charcot-Marie-Tooth disease, Type 2B: CMT is an inherited neurological disease characterized by the gradual degeneration of nerves which starts in the hands and feet and results in progressive numbness, muscle weakness and loss of function. Type 2B has an autosomal dominant inheritance and involves a defect in the gene for the protein RAB 7 located on chromosome 3. More detailed information about the symptoms, causes, and treatments of Charcot-Marie-Tooth disease, Type 2B is available below.
See full list of 6 symptoms of Charcot-Marie-Tooth disease, Type 2B
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Charcot-Marie-Tooth disease, Type 2B is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Charcot-Marie-Tooth disease, Type 2B, or a subtype of Charcot-Marie-Tooth disease, Type 2B,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
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