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  2. Complement 4 deficiency - Wikipedia

    en.wikipedia.org/wiki/Complement_4_deficiency

    Complement 4 deficiency; Specialty: Immunology: Complement tests C4 ... Complement 4 deficiency is a genetic condition affecting complement component 4. [1]

  3. Complement deficiency - Wikipedia

    en.wikipedia.org/wiki/Complement_deficiency

    C4: C4 deficiency is highly associated with systemic lupus erythematosus. [3] Aβ42, a protein involved in Alzheimer's disease, can cause activation of C4 (even in plasma deficient of C1q). [18] At least one study indicates that the genetic variation of C4 plays a role in schizophrenia. [19]

  4. Complement component 4 - Wikipedia

    en.wikipedia.org/wiki/Complement_component_4

    Complement component 4 (C4), in humans, is a protein involved in the intricate complement system, originating from the human leukocyte antigen (HLA) system. It serves a number of critical functions in immunity, tolerance, and autoimmunity with the other numerous components.

  5. Complement component 5 - Wikipedia

    en.wikipedia.org/wiki/Complement_component_5

    Complement component 5 is a protein that in humans is encoded by the C5 gene. [5] Complement component 5 is involved in the complement system. It is cleaved into C5a and C5b: C5a plays an important role in chemotaxis. [6] C5b forms the first part of the complement membrane attack complex. Deficiency is thought to cause Leiner's disease.

  6. Terminal complement pathway deficiency - Wikipedia

    en.wikipedia.org/wiki/Terminal_complement...

    Terminal complement pathway deficiency is a genetic condition affecting the complement membrane attack complex (MAC). It involves deficiencies of C5, C6, C7, and C8. (While C9 is part of the MAC, and deficiencies have been identified, [1] it is not required for cell lysis. [2]) People with this condition are prone to meningococcal infection. [3]

  7. C4A - Wikipedia

    en.wikipedia.org/wiki/C4A

    The trimer provides a surface for interaction between the antigen-antibody complex and other complement components. The alpha chain may be cleaved to release C4 anaphylatoxin, a mediator of local inflammation. Deficiency of this protein is associated with systemic lupus erythematosus and type I diabetes mellitus.

  8. A vet’s guide to Von Willebrand Disease in dogs - AOL

    www.aol.com/vet-guide-von-willebrand-disease...

    Type 1 von Willebrand Disease in dogs. Type 1 von Willebrand Disease is the most common type, and also the mildest. It occurs when dogs have a mild deficiency in all the proteins making up their ...

  9. Properdin deficiency - Wikipedia

    en.wikipedia.org/wiki/Properdin_deficiency

    In particular, the use of ELISA proves to be one of the most effective methods of detecting properdin deficiency, as the average healthy male is expected to show properdin antigen levels of around 128.0 ELISA units/ml, and obligate carrier females (recall that properdin deficiency is an X-linked disease) tend to show an average of 45.6 units/ml ...