Inherited thrombophilia, a condition most frequently caused by Factor V Leiden (G1691A) or Factor II Prothrombin (G20210A) gene mutations, is a predisposition to develop thrombosis and potentially lead to Venous Thromboembolism (VTE). Evaluation of a patient’s risk for hereditary thrombophilia through Factor II and Factor V genotyping is critical for the diagnosis and clinical management of patients with thrombophilia.

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