Table I.
Items | Results | (Refs.) |
---|---|---|
Inherited thrombophilia | Factor V Leiden mutation; Prothrombin gene (G20210) mutation; Protein C, S, and antithrombin III (AT III) deficiency; Hyperhomocysteinemia | (13) |
Acquired thrombophilia | Myeloproliferative disorders (JAK2 mutation, essential thrombocythemia, polycythemia vera, myelofibrosis); Antiphospholipid antibody syndrome/lupus anticoagulant; Paroxysmal nocturnal hemoglobinuria. | (14,15) |