Thrombophilia is a disorder of the blood coagulation system and is found with a frequency of 1/7 in the Greek population. The presence of thrombophilia multiplies the risk of circulatory system disorders such as venous thrombosis, stroke and pregnancy complications (placental abruption, early miscarriages, underweight fetuses, etc.). It can be attributed to environmental or genetic factors.
In the second case, the risk of developing thrombophilia and heart diseases in general is linked to mutations of one or more coagulation factors.
In our laboratory the molecular analysis of thrombophilia and cardiovascular diseases includes the detection of a series of mutations of coagulation factors covering a wide genetic spectrum.
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