Charcot-Marie-Tooth disease type 2A1 (Q104258): Difference between revisions
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A doença de Charcot-Marie-Tooth autossômica dominante tipo 2A1 (CMT2A1) é uma forma de doença de Charcot-Marie-Tooth axonal, uma neuropatia periférica sensitivomotora. O CMT2A se apresenta com uma fraqueza muscular mais proeminente nos membros inferiores do que nos superiores e tremor postural frequente. | |||
| description / en | description / en | ||
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. | |||
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 |
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| 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. |
