Clinical Aspects and Molecular Analysis of Chinese Patients with Wiskott-Aldrich Syndrome in Taiwan

Background: Wiskott-Aldrich syndrome (WAS) is an X-linked immunodeficiency, characterized by microthrombocytopenia, eczema and recurrent infections. More than 441 patient mutations have been described all over the world, mainly based on Caucasian and Japanese people. There have been few reported cas...

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Veröffentlicht in:	International archives of allergy and immunology 2008-01, Vol.145 (1), p.15-23
Hauptverfasser:	Lee, Wen-I, Yang, Chang-Yo, Jaing, Tang-Her, Huang, Jing-Long, Chien, Yin-Hsiu, Chang, Kuei-Wen
Format:	Artikel
Sprache:	eng
Schlagworte:	Adult Anti-Bacterial Agents - therapeutic use Asian Continental Ancestry Group - genetics Asian people Autoimmune diseases B-Lymphocytes - metabolism Biological and medical sciences Cell Line Child Child, Preschool Cytomegalovirus Fundamental and applied biological sciences. Psychology Fundamental immunology Genes Genotype Genotype & phenotype Humans Immunodeficiencies Immunodeficiencies. Immunoglobulinopathies Immunoglobulins - blood Immunoglobulins, Intravenous - therapeutic use Immunopathology Infant Leukocytes, Mononuclear - metabolism Lymphocyte Count Male Medical sciences Mutation Original Paper Phenotype Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis Stem Cell Transplantation T-Lymphocytes - metabolism Taiwan - epidemiology Wiskott-Aldrich Syndrome - genetics Wiskott-Aldrich Syndrome - immunology Wiskott-Aldrich Syndrome - metabolism Wiskott-Aldrich Syndrome - therapy Wiskott-Aldrich Syndrome Protein - genetics Wiskott-Aldrich Syndrome Protein - metabolism
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