Factor V Leiden mutation and the prothrombin gene mutation (G20210A mutation) are the most common types of hereditary thrombophilia with marked risk of venous thromboembolism (VTE) incidence. Not ...

[9] Pregnant women with the most common heritable thrombophilias (i.e., heterozygosity for factor V Leiden [OR: 8.3; 95% CI: 5.4–12.7] or the prothrombin G20210A mutation [OR: 6.8; 95% CI ...

Genetic testing showed a heterozygous prothrombin G20210A mutation. He was treated with low-molecular-weight heparin followed by dabigatran. We hypothesise that NO use may increase the risk of ...

3By contrast, there is a striking association between both V Leiden and prothrombin G20210A mutations and cerebral venous ... In some patients, particularly those with the factor V Leiden mutation, it ...