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