Charcot-Marie-Tooth disease type 2J (Q104261)

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Autosomal dominant Charcot-Marie-Tooth disease type 2J (CMT2J) is a form of axonal Charcot-Marie-Tooth disease, a peripheral sensorimotor neuropathy, characterised by a relatively late onset, papillary abnormalities and deafness, in most patients, associated with distal weakness and muscle atrophy.
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    Charcot-Marie-Tooth disease type 2J
    Autosomal dominant Charcot-Marie-Tooth disease type 2J (CMT2J) is a form of axonal Charcot-Marie-Tooth disease, a peripheral sensorimotor neuropathy, characterised by a relatively late onset, papillary abnormalities and deafness, in most patients, associated with distal weakness and muscle atrophy.

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