Acute motor sensory axonal neuropathy (Q86236): Difference between revisions
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13 August 2026
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Latest 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. |
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CID11:ID_98367105
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dki-india-ID_98367105
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Concluído
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13 August 2026
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