Charcot-Marie-Tooth disease, axonal, Type 2A (medical condition): 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.
See also:
Charcot-Marie-Tooth disease, Type 2A:
»Introduction: Charcot-Marie-Tooth disease, Type 2A
»Symptoms of Charcot-Marie-Tooth disease, Type 2A
These medical condition or symptom topics may be relevant to medical information for Charcot-Marie-Tooth disease, axonal, Type 2A:
Charcot-Marie-Tooth disease, axonal, Type 2A 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, axonal, Type 2A, or a subtype of Charcot-Marie-Tooth disease, axonal, Type 2A,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
Charcot-Marie-Tooth disease, axonal, Type 2A: Another name for Charcot-Marie-Tooth disease, Type 2A (or close medical condition association).
»Introduction: Charcot-Marie-Tooth disease, Type 2A
»Symptoms of Charcot-Marie-Tooth disease, Type 2A
Some of the symptoms of Charcot-Marie-Tooth disease, axonal, Type 2A incude:
Source - NIH
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