Charcot-Marie-Tooth disease type 2K (Q104260): Difference between revisions
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A doença de Charcot-Marie-Tooth autossômica dominante, tipo 2K (CMT2K) é uma polineuropatia periférica sensitivomotora de CMT axonal. CMT2K é uma forma rara de CMT com fenótipo leve, início durante a segunda década de vida e progressão muito lenta. | |||
| description / en | description / en | ||
Autosomal dominant Charcot-Marie-Tooth disease, type 2K (CMT2K) is an axonal CMT peripheral sensorimotor polyneuropathy. CMT2K is a rare form of CMT with a mild phenotype, onset during the second decade of life and very slow progression. | |||
Revision as of 10:07, 17 August 2026
Autosomal dominant Charcot-Marie-Tooth disease, type 2K (CMT2K) is an axonal CMT peripheral sensorimotor polyneuropathy. CMT2K is a rare form of CMT with a mild phenotype, onset during the second decade of life and very slow progression.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1720211658 |
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| English | Charcot-Marie-Tooth disease type 2K |
Autosomal dominant Charcot-Marie-Tooth disease, type 2K (CMT2K) is an axonal CMT peripheral sensorimotor polyneuropathy. CMT2K is a rare form of CMT with a mild phenotype, onset during the second decade of life and very slow progression. |
