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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