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HMSN IIA1 (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 2A1 has an autosomal dominant inheritance and involves a defect in the KIF1B gene on chromosome 1p36.
See also:
Charcot-Marie-Tooth disease, Type 2AI:
»Introduction: Charcot-Marie-Tooth disease, Type 2AI
»Symptoms of Charcot-Marie-Tooth disease, Type 2AI
These medical condition or symptom topics may be relevant to medical information for HMSN IIA1:
HMSN IIA1: Another name for Charcot-Marie-Tooth disease, Type 2AI (or close medical condition association).
»Introduction: Charcot-Marie-Tooth disease, Type 2AI
»Symptoms of Charcot-Marie-Tooth disease, Type 2AI
Some of the symptoms of HMSN IIA1 incude:
See full list of 21 symptoms of HMSN IIA1 (Charcot-Marie-Tooth disease, Type 2AI)
Search to find out more about HMSN IIA1:
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