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 / endescription / 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.
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Property / Canonical URI: https://id.who.int/icd/entity/98367105 / rank
 
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CID11:ID_98367105
Property / CURIE: CID11:ID_98367105 / rank
 
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dki-india-ID_98367105
Property / Canary Token: dki-india-ID_98367105 / rank
 
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Concluído
Property / Verification Status: Concluído / rank
 
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Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank
 
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13 August 2026
Timestamp+2026-08-13T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
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Property / Collection date: 13 August 2026 / rank
 
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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.
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    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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