Epidermolysis bullosa acquisita (Q43783): Difference between revisions
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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. |
