Epidermolysis bullosa acquisita (Q43783): Difference between revisions

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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.
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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.

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      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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