Charcot-Marie-Tooth disease type 2J (Q104261): Difference between revisions
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dki-india-ID_1498789307 | |||||||||||||||
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16 August 2026
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Latest revision as of 10:07, 17 August 2026
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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| default for all languages | ID_1498789307 |
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| English | 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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CID11:ID_1498789307
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dki-india-ID_1498789307
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Concluído
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16 August 2026
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