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Charcot-Marie-Tooth disease, axonal, Type 2B2 (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. Type 2B2 has an autosomal dominant inheritance and involves a defect located on chromosome 19.
See also:
Charcot-Marie-Tooth disease, Type 2B2:
»Introduction: Charcot-Marie-Tooth disease, Type 2B2
»Symptoms of Charcot-Marie-Tooth disease, Type 2B2
These medical condition or symptom topics may be relevant to medical information for Charcot-Marie-Tooth disease, axonal, Type 2B2:
Charcot-Marie-Tooth disease, axonal, Type 2B2 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 2B2, or a subtype of Charcot-Marie-Tooth disease, axonal, Type 2B2,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
Charcot-Marie-Tooth disease, axonal, Type 2B2: Another name for Charcot-Marie-Tooth disease, Type 2B2 (or close medical condition association).
»Introduction: Charcot-Marie-Tooth disease, Type 2B2
»Symptoms of Charcot-Marie-Tooth disease, Type 2B2
Some of the symptoms of Charcot-Marie-Tooth disease, axonal, Type 2B2 incude:
Source - NIH
Search to find out more about Charcot-Marie-Tooth disease, axonal, Type 2B2:
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