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  2. Complement deficiency - Wikipedia

    en.wikipedia.org/wiki/Complement_deficiency

    Complement deficiency is an immunodeficiency of absent or suboptimal functioning of one of the complement system proteins. [4] Because of redundancies in the immune system, many complement disorders are never diagnosed. Some studies estimate that less than 10% are identified. [5]

  3. Complement 4 deficiency - Wikipedia

    en.wikipedia.org/wiki/Complement_4_deficiency

    Complement tests C4 ... Complement 4 deficiency is a genetic condition affecting complement component 4. [1] It can present with lupus-like symptoms. [2 ...

  4. 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]

  5. 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.

  6. Hereditary angioedema - Wikipedia

    en.wikipedia.org/wiki/Hereditary_angioedema

    There are three types of hereditary angioedema (HAE). HAE types I and II are both caused by a deficiency of complement C1-inhibitor (C1-INH), a plasma protein that is an important inhibitor of several serine proteases, specially of the complement system and the contact activation/kallikrein-kinin pathway, but also the fibrinolytic system.

  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. Can I be iron deficient but not anemic? What to know. - AOL

    www.aol.com/iron-deficient-not-anemic-know...

    Before iron deficiency anemia sets in, “the body will do everything it can to retain the right number of red blood cells. So, it will deplete the storage iron before it depletes the red blood ...

  9. Complement system - Wikipedia

    en.wikipedia.org/wiki/Complement_system

    The complement system, also known as complement cascade, is a part of the humoral, innate immune system and enhances (complements) the ability of antibodies and phagocytic cells to clear microbes and damaged cells from an organism, promote inflammation, and attack the pathogen's cell membrane. [1]