| Literature DB >> 25864580 |
Zita Chovancova1,2, Milan Kuman3, Marcela Vlkova1,2, Jiri Litzman1,2.
Abstract
Wiskott-Aldrich syndrome (WAS) is a rare primary immunodeficiency disorder caused by mutations in the WAS protein (WASP) gene. Renal disease progressing to renal failure is a well-recognized complication in patients with WAS. Only a few case reports of renal transplantation have been reported to date. Here, we present a patient with a WASP mutation who suffered from severe atopic eczema, mild thrombocytopenia and only a slightly increased frequency of infections, who then developed IgA nephropathy and consequently underwent renal transplantation, which was successful. This study demonstrates that renal transplantation is possible in patients with WAS, regardless of conceivable complications.Entities:
Keywords: IgA nephropathy; Wiskott-Aldrich syndrome; immunodeficiency; renal transplantation
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Year: 2015 PMID: 25864580 DOI: 10.1111/tri.12583
Source DB: PubMed Journal: Transpl Int ISSN: 0934-0874 Impact factor: 3.782