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CMT1A (medical condition): CMT is an inherited neurological disease characterized by the gradual...more »
CMT1A is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that CMT1A, or a subtype of CMT1A,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
CMT1A: Another name for Charcot-Marie-Tooth disease, Type 1A (or close medical condition association).
»Introduction: Charcot-Marie-Tooth disease, Type 1A
»Symptoms of Charcot-Marie-Tooth disease, Type 1A
CMT1A: CMT1A is listed as a type of (or associated with) the following medical conditions in our database:
Some of the symptoms of CMT1A incude:
Source - NIH
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