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  2. Complement factor I - Wikipedia

    en.wikipedia.org/wiki/Complement_factor_I

    Complement factor I, also known as C3b/C4b inactivator, is a protein that in humans is encoded by the CFI gene. Complement factor I (factor I) is a protein of the complement system , first isolated in 1966 in guinea pig serum , [ 5 ] that regulates complement activation by cleaving cell-bound or fluid phase C3b and C4b. [ 6 ]

  3. Atypical hemolytic uremic syndrome - Wikipedia

    en.wikipedia.org/wiki/Atypical_hemolytic_uremic...

    [1] [4] [5] The complement system activation may be due to mutations in the complement regulatory proteins (factor H, factor I, or membrane cofactor protein (CD46)), [6] [5] [7] or occasionally due to acquired neutralizing autoantibody inhibitors of these complement system components (e.g. anti–factor H antibodies).

  4. 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.

  5. 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.

  6. Period-Like Cramps Can Actually Be A Sign Of A UTI - AOL

    www.aol.com/got-cramps-no-period-may-163400125.html

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  7. Fibrinogen deficiency - Wikipedia

    en.wikipedia.org/wiki/Fibrinogen_deficiency

    Fibrinogen deficiency, also known as factor I deficiency, is a rare inherited bleeding disorder related to fibrinogen function in the coagulation cascade. It is typically subclassified into four distinct fibrinogen disorders : afibrinogenemia, hypofibrinogenemia, dysfibrinogenemia, and hypodysfibrinogenemia.

  8. Hemolytic disease of the newborn (anti-Kell) - Wikipedia

    en.wikipedia.org/wiki/Hemolytic_disease_of_the...

    Newborn Screening Tests - Transfusion with donor blood during pregnancy or shortly after birth can affect the results of the Newborn Screening Tests. It is recommended to wait and retest 10–12 months after last transfusion. In some cases, DNA testing from saliva can be used to rule out certain conditions. [citation needed]

  9. Complement component 3 - Wikipedia

    en.wikipedia.org/wiki/Complement_component_3

    First, the proteolytic component of the convertase, Bb, is removed by complement regulatory proteins having decay-accelerating factor (DAF) activity. Next, C3b is broken down progressively to first iC3b, then C3c + C3dg, and then finally C3d. Factor I is the protease cleaves C3b but requires a cofactor (e.g Factor H, CR1, MCP or C4BP) for activity.