Genetic thrombophilia in young women with mesenchymal dysplasia

The pubertat period in young women with mesenchymal dysplasia in combination with the thrombogenic genetic defects in the system of hemostasis is characterized of high frequency of menstrual rhythm infringements. In the current research it was found that every second patient having undifferentiated forms of mesenchymal dysplasia and the disorders of menstruations in the pubertat period was the carrier of combined forms of innate thrombophilia. This fact allows to appropriate this category to the group of high thrombogenic risk.