Factor Ii (Prothrombin) Mutation Detection

7,000.00

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The Factor II (Prothrombin) Mutation Detection Test is a genetic test used to identify a mutation in the prothrombin gene (G20210A). This mutation can increase the risk of developing abnormal blood clots (a condition called thrombophilia). The test is typically done using a blood sample or a cheek swab.

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    Description

    Why It’s Done

    This test may be ordered if you:
    • Have experienced unexplained blood clots (especially deep vein thrombosis or pulmonary embolism).
    • Have a family history of thrombophilia or known prothrombin gene mutation.
    • Have had recurrent miscarriages, particularly in the second or third trimester.
    • Are planning hormonal therapy (e.g., oral contraceptives or hormone replacement therapy) and have a clotting history.
    • Are undergoing surgery or prolonged immobilization and have a personal/family history of clotting disorders.
    The results help assess your risk of developing blood clots and may guide treatment or lifestyle recommendations.

    Preparation

    • No special preparation is typically needed.
    • Inform your doctor if you’ve had a recent blood transfusion, as it might affect the test results.
    • Genetic counseling may be recommended before and after the test to understand the implications of the results.