Higher VTE-risk inherited thrombophilias |
Antithrombin (AT) deficiency |
Factor V Leiden (FVL) variant homozygote |
Prothrombin G20210A variant homozygote* |
Concurrent heterozygosity for both FVL and prothrombin G20210A variants |
Rare combined thrombophilias (eg, AT deficiency and FVL) |
Lower VTE-risk inherited thrombophilias |
FVL variant heterozygote |
Prothrombin G20210A variant heterozygote |
Protein C deficiency |
Protein S deficiency |
VTE: venous thromboembolism.
* Also called the prothrombin gene mutation (PGM).آیا می خواهید مدیلیب را به صفحه اصلی خود اضافه کنید؟