Both hereditary and acquired factors increase the risk of venous thromboembolism, thus the
clinical management of affected patients involves evaluation of genetic factors that …

Factor V Leiden is the most common genetic defect associated with venous
thromboembolism. Its clinical expression is limited and shows a wide intrafamilial and …

Factor V Leiden and factor II G20210A mutations are two frequent genetic risk factors
involved in venous thromboembolism (VTE). The goal of this pooled analysis of 8 case …

Factor V Leiden (F5 1691A) and prothrom-bin 20210 A (F2 20210A) are established risk
factors for venous thrombembolism, with factor V Leiden as the most commonly inherited …

Background—Homozygous or double heterozygous factor V Leiden and/or prothrombin
G20210A is a rare inherited thrombophilic trait. Whether individuals with this genetic …

Abstract Factor V Leiden (FVL) and factor II c.* 97G> A mutation are the two most common
genetic factors predisposing to hereditary thrombophilia. Being extremely rare, it used to be …

Physicians usually do not suspect pulmonary thromboembolism in younger patients except
in those who have thrombophilia. In those latter patients some special conditions such as …

Factor V Leiden and prothrombin G20210A are clinically relevant genetic risk factors for
venous thrombosis. Molecular diagnostic testing for factor V Leiden and prothrombin …

Background Point mutations in the factor V gene (factor V Leiden) and the prothrombin gene
(the substitution of A for G at position 20210) are the most common causes of inherited …

Factor V Leiden (FVLeiden) and prothrombin G20210A are the most common genetic
causes of thrombophilia and established risk factors for different clinical manifestations of …