Inflammatory polyneuropathy (Q41360): Difference between revisions

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Neuropatias periféricas inflamatórias adquiridas são de etiologia imune presumida e são classificadas com base em seu curso clínico: polineuropatia inflamatória desmielinizante aguda (PIDA ou síndrome de Guillain-Barré) com o déficit motor atingindo um nível máximo em 28 dias e polineuropatia inflamatória desmielinizante crônica (PIDC) que tem um curso lentamente progressivo de dois ou mais meses ou um curso remitente recorrente. Existem muitas variantes de PIDA e PIDC.
description / endescription / en
 
Acquired inflammatory peripheral neuropathies are of a presumed immune etiology and are classified on the basis of their clinical course: acute inflammatory demyelinating polyneuropathy (AIDP or Guillain-Barré syndrome) with the motor deficit reaching a maximal level by 28 days, and chronic inflammatory demyelinating polyneuropathy (CIDP) which has a slowly progressive course of two or more months or a relapsing remitting course. There are many variants of AIDP and CIDP.
Property / Canonical URI
 
Property / Canonical URI: https://id.who.int/icd/entity/1719029386 / rank
 
Normal rank
Property / CURIE
 
CID11:8C01
Property / CURIE: CID11:8C01 / rank
 
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Property / Canary Token
 
dki-india-8C01
Property / Canary Token: dki-india-8C01 / rank
 
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Property / Verification Status
 
Concluído
Property / Verification Status: Concluído / rank
 
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Property / Knowledge Architect
 
Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank
 
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Property / Collection date
 
13 August 2026
Timestamp+2026-08-13T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0
Property / Collection date: 13 August 2026 / rank
 
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Property / Linked ICD 10
 
Property / Linked ICD 10: G61 / rank
 
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Latest revision as of 07:29, 13 August 2026

Acquired inflammatory peripheral neuropathies are of a presumed immune etiology and are classified on the basis of their clinical course: acute inflammatory demyelinating polyneuropathy (AIDP or Guillain-Barré syndrome) with the motor deficit reaching a maximal level by 28 days, and chronic inflammatory demyelinating polyneuropathy (CIDP) which has a slowly progressive course of two or more months or a relapsing remitting course. There are many variants of AIDP and CIDP.
Language Label Description Also known as
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8C01
    English
    Inflammatory polyneuropathy
    Acquired inflammatory peripheral neuropathies are of a presumed immune etiology and are classified on the basis of their clinical course: acute inflammatory demyelinating polyneuropathy (AIDP or Guillain-Barré syndrome) with the motor deficit reaching a maximal level by 28 days, and chronic inflammatory demyelinating polyneuropathy (CIDP) which has a slowly progressive course of two or more months or a relapsing remitting course. There are many variants of AIDP and CIDP.

      Statements

      CID11:8C01
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      dki-india-8C01
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      Concluído
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      13 August 2026
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