Results for « 腓骨肌萎缩征 » (cmn)
14208587-n
腓骨肌萎缩征
Charcot-Marie-Tooth disease, hereditary motor and sensory neuropathy
     a form of neuropathy that can begin between childhood and young adulthood; characterized by weakness and atrophy of the muscles of the hands and lower legs; progression is slow and individuals affected can have a normal life span; inheritance is X-linked recessive or X-linked dominant

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