Epidermolysis bullosa acquisita (Q43783): Difference between revisions
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| description / pt-br | description / 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 / en | description / 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. | |||
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 |
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| 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. |
