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Epidermolysis bullosa acquisita: current diagnosis and therapy

Epidermolysis bullosa acquisita (EBA) is an acquired, autoimmune subepidermal blistering disease with an approximate prevalence of 0,2/million people. The hallmark of EBA is the presence of autoantibodies (mainly IgG class) to anchoring fibril collagen (type VII collagen) located at the dermal-epide...

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Hlavní autoři: Christine R. Mehren, Robert Gniadecki
Médium: Artigo
Jazyk:Inglês
Vydáno: PAGEPress Publications 2011-11-01
Edice:Dermatology Reports
Témata:
On-line přístup:http://www.pagepress.org/journals/index.php/dr/article/view/2476
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