Membranoproliferative glomerulonephritis in Wiskott-Aldrich syndrome: improvement by alternative day methylprednisolone therapy.

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[The Wiskott-Aldrich syndrome].

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BACKGROUND Wiskott Aldrich syndrome (WAS) is a rare X-linked primary immunodeficiency. This complex disease is characterised by microthrombocytopenia, recurrent infections, eczema and is associated with a high incidence of autoimmunity and of lymphoid malignancies. WAS is attracting growing attention not only because it highlights the rich cellular and systems biology revolving around cytoskele...

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Wiskott-Aldrich syndrome (WAS) is a fully penetrant X-linked recessive disorder characterized by thrombocytopenia with small platelets, eczema, and defects of both T-cell and B-cell immunity. Obligate carriers of this disorder show no signs of the gene defect because in the cell lineages primarily affected by the disorder they demonstrate preferential use of the normal, nonmutant X as the activ...

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ژورنال

عنوان ژورنال: Japanese Journal of Clinical Immunology

سال: 1993

ISSN: 0911-4300,1349-7413

DOI: 10.2177/jsci.16.305