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Factor II (Prothrombin) - Molecular Detection of G20210A Mutation

Includes 1 test
Blood
55€

Molecular screening of the coagulation factor II gene G20210A (prothrombin) is performed to assess the risk of thrombosis in asymptomatic patients with a familial history or in patients who have already experienced a thromboembolic episode.

Prothrombin or otherwise factor II is a key enzyme in the processes of hemostasis and thrombosis. Recently, a point mutation (replacement of guanine by adenosine at nucleotide position 20210) has been discovered that has been associated with deep vein thrombosis.Heterozygous carriers of the mutation have a 3 times higher risk of thrombosis while for homozygous mutants, this relative risk is being investigated.

This mutation is the second most common cause of hereditary thrombophilia and in the Caucasian race it is 1-2%.

Thrombophilia is an acquired or congenital disorder associated with thrombosis. The clinical appearance of an underlying thrombophilia mainly involves venous thromboembolism, which is manifested as deep vein thrombosis, pulmonary embolism, or superficial vein thrombosis. Other events associated with thrombophilia include prolonged (recurrent) miscarriages and complications of pregnancy such as severe preeclampsia, placental abruption, and fetal endometrial death. The demographic and environmental characteristics that contribute to the risk of venous thromboembolism in people predisposed to thrombophilia include: old age, gender (more commonly in men), obesity, surgery, trauma, hospitalization, malignant neoplasms, prolonged immobility (such as long plane trips), use of certain medications (such as contraceptives, estrogens, tamoxifen and raloxifene) and certain drugs used to treat hypoglycemia equality.

 

 
 
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Additional information
Tests includedIncludes 1 test
Sample Blood
Procedure completion test
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