Epidermolysis bullosa acquisita (Q43783): Difference between revisions

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description / pt-brdescription / pt-br
 
A epidermólise bolhosa adquirida é uma doença bolhosa adquirida não familiar caracterizada pela presença de autoanticorpos para colágeno VII na zona da membrana basal da epiderme, como demonstrado por imunofluorescência direta. Há um amplo espectro de manifestações clínicas, incluindo uma variante induzida por trauma e uma variante mais inflamatória.
description / endescription / en
 
Epidermolysis bullosa acquisita is an acquired non-familial blistering disease characterised by the presence of autoantibodies to collagen VII at the epidermal basement membrane zone, as demonstrated by direct immunofluorescence. There is a wide spectrum of clinical manifestations including a trauma-induced variant and a more inflammatory variant.
Property / Canonical URI
 
Property / Canonical URI: https://id.who.int/icd/entity/2034586329 / rank
 
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Property / CURIE
 
CID11:EB43
Property / CURIE: CID11:EB43 / rank
 
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Property / Canary Token
 
dki-india-EB43
Property / Canary Token: dki-india-EB43 / 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: L12.3 / rank
 
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Latest revision as of 10:56, 13 August 2026

Epidermolysis bullosa acquisita is an acquired non-familial blistering disease characterised by the presence of autoantibodies to collagen VII at the epidermal basement membrane zone, as demonstrated by direct immunofluorescence. There is a wide spectrum of clinical manifestations including a trauma-induced variant and a more inflammatory variant.
Language Label Description Also known as
default for all languages
EB43
    English
    Epidermolysis bullosa acquisita
    Epidermolysis bullosa acquisita is an acquired non-familial blistering disease characterised by the presence of autoantibodies to collagen VII at the epidermal basement membrane zone, as demonstrated by direct immunofluorescence. There is a wide spectrum of clinical manifestations including a trauma-induced variant and a more inflammatory variant.

      Statements

      CID11:EB43
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      dki-india-EB43
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      Concluído
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      13 August 2026
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