Back to matchesWe found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleOmenn syndrome due to mutation of the RAG2 gene.AuthorsKtiouet, S; Bertrand, Y; Rival-Tringali, AL; Kanitakis, J; Malcus, C; Poitevin, F; Picard, C; Claudy, A; Faure, MAbstractA letter to the editor is presented which discusses the diagnosis of diffuse, finely scaly erythroderma in a newborn baby girl.SubjectsLETTERS to the editor; IMMUNOLOGICAL deficiency syndromesPublicationJournal of the European Academy of Dermatology & Venereology, 2009, Vol 23, Issue 12, p1449ISSN0926-9959Publication typeLetterDOI10.1111/j.1468-3083.2009.03232.x