This article briefly presents the existing types of thrombophilia, which are based on both hereditary and acquired forms of hemostasis.
The most common and genetically determined (hereditary) cause of thrombophilia during pregnancy is APC-P and factor V mutation - Leidena and the progression of the prothrombin gene G20210A
Among the acquired forms of thrombophilia, the most common is the APS, which occurs in a wide range of diseases, so it is regarded as a nonspecific process, in which the blood pressure decreases, leading to a blockade of microcirculation in organs and tissues.
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