Frequently Asked Questions
Everything you wonder about thrombophilia
Thrombophilia is an inherited or acquired condition in which blood has an increased tendency to clot. It can arise from genetic factors (Factor V Leiden, prothrombin mutation, etc.) or from acquired causes.
People with a family history of thrombosis, recurrent pregnancy loss, thrombosis at a young age, women planning to use oral contraceptives or HRT, and those needing pre-surgical risk assessment should be tested.
It is performed on a small blood sample drawn from your arm. In our laboratory, DNA is isolated and genetic mutations (Factor V Leiden, Prothrombin G20210A, MTHFR, etc.) are analyzed using PCR and sequencing.
Results are usually ready within 7-10 business days. The report covers the identified mutations and clinical recommendations.
Yes, some types (Factor V Leiden, prothrombin mutation, Protein C/S deficiency, antithrombin deficiency) are inherited, and screening family members is recommended.
Thrombophilia is usually a lifelong condition, but it can be managed effectively with blood thinners, lifestyle changes and regular follow-up. Treatment is personalized to the mutation type and clinical picture.
Thrombophilia can increase the risk of miscarriage, preeclampsia, placental abruption and other pregnancy complications. Close medical follow-up is essential for patients planning pregnancy.
Yes, regular exercise generally helps circulation. However, contact sports are best avoided, especially while on blood thinners. Ask your doctor to build a suitable exercise plan.
The fee depends on the scope of the requested panel. For detailed pricing, contact us at +90 312 920 13 62 or [email protected].
Usually no fasting or special preparation is required. If you use blood thinners or other medications, inform the laboratory. Your physician will advise on your specific situation.