Acute motor sensory axonal neuropathy (Q86236): Difference between revisions
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Neuropatia axonal sensitivo-motora aguda (AMSAN) é uma forma axonal sensitivo-motora da síndrome de Guillain-Barré (GBS) com um quadro clínico (fraqueza muscular e déficits sensoriais) semelhante ao da forma desmielinizante mais frequente de SGB (polirradiculoneuropatia desmielinizante inflamatória aguda; AIDP), mas com um curso de doença mais grave. | |||
| description / en | description / en | ||
Acute motor-sensory axonal neuropathy (AMSAN) is a motor-sensory, axonal form of Guillain-Barré syndrome (GBS) with a clinical picture (muscle weakness and sensory deficits) similar to that of the more frequent demyelinating form of GBS (acute inflammatory demyelinating polyradiculoneuropathy; AIDP) but with a more severe disease course. | |||
Revision as of 11:36, 15 August 2026
Acute motor-sensory axonal neuropathy (AMSAN) is a motor-sensory, axonal form of Guillain-Barré syndrome (GBS) with a clinical picture (muscle weakness and sensory deficits) similar to that of the more frequent demyelinating form of GBS (acute inflammatory demyelinating polyradiculoneuropathy; AIDP) but with a more severe disease course.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_98367105 |
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| English | Acute motor sensory axonal neuropathy |
Acute motor-sensory axonal neuropathy (AMSAN) is a motor-sensory, axonal form of Guillain-Barré syndrome (GBS) with a clinical picture (muscle weakness and sensory deficits) similar to that of the more frequent demyelinating form of GBS (acute inflammatory demyelinating polyradiculoneuropathy; AIDP) but with a more severe disease course. |
