- Complement 3 deficiency
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Complement 3 deficiency Classification and external resources OMIM 120700 DiseasesDB 1869 Complement 3 deficiency is a genetic condition affecting complement component 3.
It can cause systemic lupus erythematosus-like symptoms.[1]
It can lead to an increase in pyogenic infections[2] from encapsulated bacteria.[3]
References
- ^ Matsuyama W, Nakagawa M, Takashima H, Muranaga F, Sano Y, Osame M (December 2001). "Molecular analysis of hereditary deficiency of the third component of complement (C3) in two sisters". Intern. Med. 40 (12): 1254–8. doi:10.2169/internalmedicine.40.1254. PMID 11813855. http://joi.jlc.jst.go.jp/JST.Journalarchive/internalmedicine1992/40.1254?from=PubMed.
- ^ Parija (2009-01-01). Textbook of Microbiology & Immunology. Elsevier India. pp. 125–. ISBN 9788131221631. http://books.google.com/books?id=HcgGLfxDJSQC&pg=PA125. Retrieved 13 November 2010.
- ^ Sherwood L. Gorbach; John G. Bartlett; Neil R. Blacklow (2004). Infectious diseases. Lippincott Williams & Wilkins. pp. 11–. ISBN 9780781733717. http://books.google.com/books?id=91altE1evAsC&pg=PA11. Retrieved 30 May 2010.
Immune disorders: Lymphoid and complement immunodeficiency (D80–D85, 279.0–4) Primary IgA deficiency · IgG deficiency · IgM deficiency · Hyper IgM syndrome (2, 3, 4, 5) · Wiskott-Aldrich syndrome · Hyper-IgE syndromeOtherthymic hypoplasia: hypoparathyroid (Di George's syndrome) · euparathyroid (Nezelof syndrome, Ataxia telangiectasia)x-linked: X-SCID
autosomal: Adenosine deaminase deficiency · Omenn syndrome · ZAP70 deficiency · Bare lymphocyte syndromeAcquired Leukopenia:
LymphocytopeniaComplement deficiency C1-inhibitor (Angioedema/Hereditary angioedema) · Complement 2 deficiency/Complement 4 deficiency · MBL deficiency · Properdin deficiency · Complement 3 deficiency · Terminal complement pathway deficiency · Paroxysmal nocturnal hemoglobinuria · Complement receptor deficiencyCategories:- Medicine stubs
- Complement deficiency
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