Charcot-Marie-Tooth disease type 4A (Q104652): Difference between revisions
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A doença de Charcot-Marie-Tooth, tipo 4A (CMT4A) é uma forma grave de início precoce de polineuropatia periférica sensitivomotora da CMT desmielinizante caracterizada por retardo motor grave e escoliose progressiva. CMT4A é considerada a mais frequente de todas as formas autossômicas recessivas de CMT. | |||
| description / en | description / en | ||
Charcot-Marie-Tooth disease, type 4A (CMT4A) is a severe, early-onset form of demyelinating CMT peripheral sensorimotor polyneuropathy characterised by severe motor retardation and progressive scoliosis. CMT4A is considered as the most frequent of all autosomal recessive forms of CMT. | |||
Revision as of 10:31, 17 August 2026
Charcot-Marie-Tooth disease, type 4A (CMT4A) is a severe, early-onset form of demyelinating CMT peripheral sensorimotor polyneuropathy characterised by severe motor retardation and progressive scoliosis. CMT4A is considered as the most frequent of all autosomal recessive forms of CMT.
| Language | Label | Description | Also known as |
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| default for all languages | ID_1476665103 |
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| English | Charcot-Marie-Tooth disease type 4A |
Charcot-Marie-Tooth disease, type 4A (CMT4A) is a severe, early-onset form of demyelinating CMT peripheral sensorimotor polyneuropathy characterised by severe motor retardation and progressive scoliosis. CMT4A is considered as the most frequent of all autosomal recessive forms of CMT. |
