Charcot-Marie-Tooth disease type 2I (Q104262): Difference between revisions
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dki-india-ID_1858507973 | |||||||||||||||
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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 2I (CMT2I) is a form of axonal Charcot-Marie-Tooth disease, a peripheral sensorimotor neuropathy, characterised by a late onset with severe sensory loss (paraesthesia and hypoesthesia) associated with distal weakness, mainly of the legs, and absent or reduced deep tendon reflexes.
| Language | Label | Description | Also known as |
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| default for all languages | ID_1858507973 |
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| English | Charcot-Marie-Tooth disease type 2I |
Autosomal dominant Charcot-Marie-Tooth disease type 2I (CMT2I) is a form of axonal Charcot-Marie-Tooth disease, a peripheral sensorimotor neuropathy, characterised by a late onset with severe sensory loss (paraesthesia and hypoesthesia) associated with distal weakness, mainly of the legs, and absent or reduced deep tendon reflexes. |
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CID11:ID_1858507973
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dki-india-ID_1858507973
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Concluído
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16 August 2026
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