Nonoyama S, Ochs H D
Department of Pediatrics, School of Medicine, Tokyo Medical and Dental University, 1-5-45, Yushima, Bunkyo-ku, Tokyo, 113-8519, Japan.
Curr Allergy Asthma Rep. 2001 Sep;1(5):430-7. doi: 10.1007/s11882-001-0028-0.
Wiskott-Aldrich syndrome (WAS) is an X-linked immunodeficiency characterized by thrombocytopenia with small platelets, eczema, recurrent infections, autoimmune disorders, IgA nephropathy, and an increased incidence of hematopoietic malignancies. The identification of the responsible gene, WASP (Wiskott-Aldrich Syndrome Protein), revealed clinical heterogeneity of the syndrome, and showed that X-linked thrombocytopenia without, or with only mild immunodeficiency and eczema, is also caused by mutations of WASP. The study of WASP and its mutations demonstrates how a single gene defect can cause multiple and complex clinical symptoms.
威斯科特-奥尔德里奇综合征(WAS)是一种X连锁免疫缺陷病,其特征为血小板减少伴小血小板、湿疹、反复感染、自身免疫性疾病、IgA肾病以及造血系统恶性肿瘤发病率增加。致病基因WASP(威斯科特-奥尔德里奇综合征蛋白)的鉴定揭示了该综合征的临床异质性,并表明无免疫缺陷或仅有轻度免疫缺陷及湿疹的X连锁血小板减少症也由WASP突变引起。对WASP及其突变的研究表明了单个基因缺陷如何导致多种复杂的临床症状。