Acute inflammatory demyelinating polyneuropathy (Q41364): Difference between revisions
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Fraqueza progressiva dos membros ao longo de alguns dias a 28 dias, déficit simétrico, arreflexia, distúrbio sensorial ausente ou leve, proteína do líquido cefalorraquidiano elevada e redução das velocidades de condução nervosa são as características principais. O transtorno pode ser precedido por infecção respiratória superior ou gastrointestinal ou imunização 1 a 4 semanas antes do início da doença. A paralisia bifacial pode estar presente. | |||
| description / en | description / en | ||
Progressive weakness of the limbs over a few days to 28 days, symmetrical deficit, areflexia, absent or mild sensory disturbance, elevated cerebrospinal fluid protein, and slowing of nerve conduction velocities are the cardinal features. The disorder may be preceded by upper respiratory or gastrointestinal infection or immunization 1 to 4 weeks prior to onset of the illness. Bifacial palsy may be present. | |||
Revision as of 07:30, 13 August 2026
Progressive weakness of the limbs over a few days to 28 days, symmetrical deficit, areflexia, absent or mild sensory disturbance, elevated cerebrospinal fluid protein, and slowing of nerve conduction velocities are the cardinal features. The disorder may be preceded by upper respiratory or gastrointestinal infection or immunization 1 to 4 weeks prior to onset of the illness. Bifacial palsy may be present.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | 8C01.0 |
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| English | Acute inflammatory demyelinating polyneuropathy |
Progressive weakness of the limbs over a few days to 28 days, symmetrical deficit, areflexia, absent or mild sensory disturbance, elevated cerebrospinal fluid protein, and slowing of nerve conduction velocities are the cardinal features. The disorder may be preceded by upper respiratory or gastrointestinal infection or immunization 1 to 4 weeks prior to onset of the illness. Bifacial palsy may be present. |
