Charcot-Marie-Tooth disease type 2D (Q104264): Difference between revisions
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dki-india-ID_1617529678 | |||||||||||||||
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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 2D (CMT2D) is a form of axonal Charcot-Marie-Tooth disease, a peripheral sensorimotor neuropathy, characterised by distal weakness primarily and predominantly occurring in the upper limbs and tendon reflexes absent or reduced in the arms and decreased in the legs. Progression is slow.
| Language | Label | Description | Also known as |
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| default for all languages | ID_1617529678 |
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| English | Charcot-Marie-Tooth disease type 2D |
Autosomal dominant Charcot-Marie-Tooth disease type 2D (CMT2D) is a form of axonal Charcot-Marie-Tooth disease, a peripheral sensorimotor neuropathy, characterised by distal weakness primarily and predominantly occurring in the upper limbs and tendon reflexes absent or reduced in the arms and decreased in the legs. Progression is slow. |
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CID11:ID_1617529678
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dki-india-ID_1617529678
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Concluído
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16 August 2026
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