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Results 1 - 10 of 37 for Prothrombin deficiency
  1. Prothrombin deficiency is a bleeding disorder that slows the blood clotting process. People with this condition often experience ...
  2. Prothrombin deficiency is a disorder caused by a lack of a protein in the blood called prothrombin. It ... or factor II, is one such coagulation factor. Prothrombin deficiency runs in families (inherited) and is very rare. ...
  3. ... Partial thromboplastin time ( PTT ) Plasma factor VII activity Prothrombin time ( PT ) Mixing study, a special PTT test to confirm factor VII deficiency
  4. ... the F2 gene have been found to cause prothrombin deficiency. Most of these mutations change one protein building ... analysis of nine novel mutations in patients with prothrombin deficiency. Thromb Haemost. 2000 Dec;84(6):989-97. ...
  5. ... is not inherited. F7 deficiency Hypoproconvertinemia Proconvertin deficiency Prothrombin conversion accelerator deficiency Serum prothrombin conversion accelerator deficiency Genetic Testing Registry: ...
  6. Bleeding Disorders (National Library of Medicine)  
    Normally, if you get hurt, your body forms a blood clot to stop the bleeding. For blood to clot, your body needs cells called platelets and proteins known as clotting ...
  7. Rare Clotting Factor Deficiencies (World Federation of Hemophilia)  
    Bleeding Disorders/Specifics ... Bleeding Disorders ... Vitamin K/Learn More ... Vitamin K ... World Federation of Hemophilia
  8. ... Hyperprothrombinemia Prothrombin G20210A Thrombophilia Genetic Testing Registry: Congenital prothrombin deficiency Prothrombin-related thrombophilia National Organization for Rare Disorders ( ...
  9. ... Congenital platelet function defects Disseminated intravascular coagulation (DIC) Prothrombin deficiency Factor V deficiency Factor VII deficiency Factor X ...
  10. ... Hoek B, Rosendaal FR. Factor V Leiden mutation, prothrombin gene mutation, and deficiencies in coagulation inhibitors associated with Budd-Chiari syndrome ...
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