Abstract
Thrombosis significantly impact on the overall morbidity and mortality in all age groups. The cause of stroke remains unknown in approximately 20% of cases. The article presents a brief review of the most common hereditary and acquired thrombophilia. One of the methods of etiologic diagnostic of thrombophilia is revealing the markers of hereditary or acquired diseases with molecular and genetic typing of haemostatic system factors. We present a case report of recurrent cerebral thrombosis in both vascular regions of the brain due to multigenic thrombophilia. The final objective of the research is not only to reveal the possible causes and risk factors of thrombosis but also to implement effective secondary prevention of thrombotic events.
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