Epidermolysis bullosa acquisita following skin graft in donor and graft sites: A case report

Epidermolysis bullosa acquisita is a rare mucocutaneous autoimmune blistering disorder which usually presents in adulthood. The disease is mediated by antibodies against type VII collagen, though the precise inciting factors for autoantibody formation are unknown. Here, we present the case of a 69-y...

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Main Authors: Joyce Xia (Author), Alice J. Tan (Author), Gunnlaugur P. Nielsen (Author), Ruth K. Foreman (Author), Mai Hoang (Author), Sean A. Hickey (Author), Daniela Kroshinsky (Author)
Format: Knjiga
Izdano: Elsevier, 2023-10-01T00:00:00Z.
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