🔬Visit our branches until December 31 and get -50% discount on Genetic testing for Hereditary Thrombophilia‼
👉Thrombophilia is a condition of the body in which the ability of blood to clot is increased.
👉Thrombophilia is mostly caused by genetics and is asymptomatic. The appearance of symptoms is associated with the formation of clots in the body, as a result of which the risk of deep vein thrombosis and pulmonary embolism increases.
👉Thrombophilia may increase the risk of developing thrombosis in pregnant women, so timely diagnosis can prevent such complications as:
⚠️ prematurely terminated pregnancies;
⚠️eclampsia/preeclampsia;
⚠️Premature discharge of a normally attached placenta; birth of a premature newborn;
⚠️ fetal growth retardation and others.
🔍Genetic thrombophilia 6 gene mutation is diagnosed by PCR method.
🔬 The research is conducted on the following genes:
✅FACTOR V LEIDEN (G1691A)
✅FACTOR V (H1299R)
✅FII (G20210A) (PROTHROMBIN)
✅MTHFR (A1298C)
✅MTHFR (C6777T)
✅ PAI-1 4G/5G
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