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  2. Fibrinogen - Wikipedia

    en.wikipedia.org/wiki/Fibrinogen

    Fibrinogen (coagulation factor I) is a glycoprotein complex, produced in the liver, [1] that circulates in the blood of all vertebrates. [2] During tissue and vascular injury, it is converted enzymatically by thrombin to fibrin and then to a fibrin-based blood clot. Fibrin clots function primarily to occlude blood vessels to stop bleeding ...

  3. Factor VIII - Wikipedia

    en.wikipedia.org/wiki/Factor_VIII

    Coagulation factor VIII (Factor VIII, FVIII, also known as anti-hemophilic factor (AHF)) is an essential blood clotting protein. In humans, it is encoded by F8 gene . [ 5 ] [ 6 ] Defects in this gene result in hemophilia A , an X-linked bleeding disorder .

  4. Coagulation - Wikipedia

    en.wikipedia.org/wiki/Coagulation

    If a coagulation factor is part of the contact activation or tissue factor pathway, a deficiency of that factor will affect only one of the tests: Thus hemophilia A, a deficiency of factor VIII, which is part of the contact activation pathway, results in an abnormally prolonged aPTT test but a normal PT test. Deficiencies of common pathway ...

  5. Hyperfibrinolysis - Wikipedia

    en.wikipedia.org/wiki/Hyperfibrinolysis

    The classical coagulation tests such as PT (prothrombin time), aPTT (activated partial thromboplastin time) or thrombin time are not very sensitive for hyperfibrinolysis, and influenced by numerous other variables. The euglobulin lysis time test is very time-consuming and complex.

  6. Thromboelastometry - Wikipedia

    en.wikipedia.org/wiki/Thromboelastometry

    EXTEM test mildly activates haemostasis via the physiological activator tissue factor. The result is influenced by extrinsic coagulation factors, platelets and fibrinogen. EXTEM is a screening test for the (extrinsic) haemostasis system. This assay is not influenced by heparin (heparin inhibitor included in the EXTEM reagent).

  7. Haemophilia - Wikipedia

    en.wikipedia.org/wiki/Haemophilia

    Haemophilia A is a recessive X-linked genetic disorder resulting in a deficiency of functional clotting Factor VIII. [39] Haemophilia B is also a recessive X-linked genetic disorder involving a lack of functional clotting Factor IX. [42] Haemophilia C is an autosomal genetic disorder involving a lack of functional clotting Factor XI.

  8. Coagulation screen - Wikipedia

    en.wikipedia.org/wiki/Coagulation_screen

    TCT or fibrinogen assay for final common pathway (THROMBIN TIME) Two other tests are regularly performed at the same time: blood count, to detect other hematological abnormalities; liver function tests to exclude liver disease as a cause of coagulation factor deficiency; These tests may miss mild abnormalities but they will detect major disorders.

  9. Fibrinolysis - Wikipedia

    en.wikipedia.org/wiki/Fibrinolysis

    FDPs compete with thrombin, and thus slow down clot formation by preventing the conversion of fibrinogen to fibrin. This effect can be seen in the thrombin clotting time (TCT) test, which is prolonged in a person that has active fibrinolysis. FDPs, and a specific FDP, the D-dimer, can be measured using antibody-antigen technology. This is more ...

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