Charcot-Marie-Tooth disease type 2I (Q104262): Difference between revisions
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A doença de Charcot-Marie-Tooth autossômica dominante tipo 2I (CMT2I) é uma forma de doença de Charcot-Marie-Tooth axonal, uma neuropatia periférica sensitivomotora, caracterizada por um início tardio de perda sensitiva grave (parestesia e hipoestesia) associada a fraqueza distal, principalmente das pernas e reflexos tendinosos profundos ausentes ou reduzidos. | |||
| description / en | description / en | ||
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. | |||
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 |
|---|---|---|---|
| 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. |
