Literature DB >> 25864580

Successful renal transplantation in a patient with a Wiskott-Aldrich syndrome protein (WASP) gene mutation.

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.
© 2015 Steunstichting ESOT.

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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


  1 in total

1.  Immune Complex-Mediated Glomerulonephritis in a Patient with Wiskott-Aldrich Syndrome.

Authors:  Tomonari Shigemura; Yozo Nakazawa; Hisashi Shimojo; Norimoto Kobayashi; Kazunaga Agematsu
Journal:  J Clin Immunol       Date:  2016-03-10       Impact factor: 8.317

  1 in total

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