- Complement 4 deficiency
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Complement 4 deficiency Classification and external resources OMIM 120820 DiseasesDB 1873 Complement 4 deficiency is a genetic condition affecting complement component 4.[1]
Complement tests C4 (C) FB (A) C3 CH50 Conditions · ↓ ↓ ↓ PSG, C3 NeF AA ↓ · ↓ · HA, C4D · · · ↓ TCPD ↓ · /↓ ↓ ↓ SLE ↑ ↑ ↑ ↑ inflammation It can present with lupus-like symptoms.[2]
References
- ^ Parija. Textbook of Microbiology & Immunology. Elsevier India. pp. 125–. ISBN 9788131221631. http://books.google.com/books?id=HcgGLfxDJSQC&pg=PA125. Retrieved 13 November 2010.
- ^ David L. Rimoin; J. Michael Connor; Reed E. Pyeritz; Bruce R. Korf (15 December 2006). Principles and Practice of Medical Genetics: Continually Updated Online Reference. Elsevier Health Sciences. pp. 1860–. ISBN 9780443068706. http://books.google.com/books?id=uc9fmqARPf8C&pg=PA1860. Retrieved 13 November 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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