Charcot-Marie-Tooth disease type 2A1 (Q104258): Difference between revisions
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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 2A1 (CMT2A1) is a form of axonal Charcot-Marie-Tooth disease, a peripheral sensorimotor neuropathy. CMT2A presents with a more prominent muscle weakness in lower than upper limbs and frequent postural tremor.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_2087067372 |
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| English | Charcot-Marie-Tooth disease type 2A1 |
Autosomal dominant Charcot-Marie-Tooth disease type 2A1 (CMT2A1) is a form of axonal Charcot-Marie-Tooth disease, a peripheral sensorimotor neuropathy. CMT2A presents with a more prominent muscle weakness in lower than upper limbs and frequent postural tremor. |
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CID11:ID_2087067372
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dki-india-ID_2087067372
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Concluído
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16 August 2026
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