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Lookup NU author(s): Professor Andrew GenneryORCiD, Dr Terence Flood, Dr Mario Abinun, Professor Andrew Cant
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Congenital immunodeficiency in hyper IgE syndrome is characterised by a markedly raised IgE level, recurrent staphylococcal skin infection and pneumatoceles. Standard treatments include anti-staphylococcal antibiotics. We report a severely affected patient in whom successful bone marrow transplantation was followed by reappearance of the immunodeficiency. We conclude that bone marrow transplantation does not cure the immunological features of the hyper IgE syndrome.
Author(s): Gennery AR, Flood TJ, Abinun M, Cant AJ
Publication type: Article
Publication status: Published
Journal: Bone Marrow Transplantation
Year: 2000
Volume: 25
Issue: 12
Pages: 1303-1305
ISSN (print): 0268-3369
ISSN (electronic): 1476-5365
Publisher: Nature Publishing Group
URL: http://dx.doi.org/10.1038/sj.bmt.1702446
DOI: 10.1038/sj.bmt.1702446
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