An Infantile Case of Early Manifestation of SLE-like Symptoms in Complete C1q Deficiency
Author:
Affiliation:
1. Department of Pediatrics, Graduate School of Medicine, Nippon Medical School
2. Department of Pediatrics, Nippon Medical School
Publisher
Medical Association of Nippon Medical School
Subject
General Medicine
Link
http://www.jstage.jst.go.jp/article/jnms/78/5/78_5_322/_pdf
Reference18 articles.
1. 1. Walport MJ, Davies KA, Botto M: C1q and systemic lupus erythematosus. Immunobiology 1998; 199: 265-285.
2. 2. Berkel AI, et al.: Molecular, genetic and epidemiologic studies on selective complete C1q deficiency in Turkey. Immunobiology 2000; 201: 347-355.
3. 3. Barilla-LaBarca ML, Atkinson JP: Rheumatic syndromes associated with complement deficiency. Current opinion in rheumatology 2003; 15: 55-60.
4. 4. Arkwright PD, Abinun M, Cant AJ: Autoimmunity in human primary immunodeficiency diseases. Blood 2002; 99: 2694-2702.
5. 5. Jonsson G, et al.: Rheumatological manifestations, organ damage and autoimmunity in hereditary C2 deficiency. Rheumatology 2007; 46: 1133-1139.
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