Absence of Epidermal Antibodies in Stevens–Johnson Syndrome/Toxic Epidermal Necrolysis Patients but Beware of Single Positive Results

Background. Stevens–Johnson syndrome (SJS) and toxic epidermal necrolysis (TEN) are rare and potentially life-threatening mucocutaneous blistering diseases that clinically can resemble autoimmune bullous diseases. Moreover, it has been shown that autoantibodies against epidermal proteins are present...

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Bibliographic Details
Main Authors: Gilles F. H. Diercks, Joost M. Meijer, Maria C. Bolling, Sonja M. H. J. Scholtens-Jaegers, Jeroen Bremer, Barbara Horvath
Format: Article
Language:English
Published: Wiley 2024-01-01
Series:Dermatology Research and Practice
Online Access:http://dx.doi.org/10.1155/2024/5504462
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