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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Bibliographic Details
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: Book
Published: Elsevier, 2023-10-01T00:00:00Z.
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3rd Floor Main Library

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Call Number: A1234.567
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