F0004
Factor II (Prothrombin) Mutation Detection
Test Details: Prothrombin gene mutation (or Factor II mutation or Prothrombin G20210A) is an inherited condition that increases predisposition to develop abnormal blood clots in the veins (deep vein thrombosis or DVT) and lungs (pulmonary embolism or PE). The test is indicated in patients with history of venous thrombosis, thrombosis at different sites, coronary artery disease, stroke of unknown etiology, women with recurrent pregnancy loss, unexplained severe pre-eclampsia, placenta abruption, fetal growth retardation.
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Category
Molecular Genetics
Pre-test Information
Clinical history is mandatory.
Report Delivery
4 working days
Gender
All
Organ
Blood
Factor II (Prothrombin) Mutation Detection
5000
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