Gebelite protein-s eksikliği ile ilişkili serebral sinüs trombozu: nadir bir olgu sunumu

Abstract

Hereditary thrombophylic mutations are seen in 10% of the general population and many cases are diagnosed as a result of complications that occur during pregnancy. Of these, Protein S deficiency is a rare hereditary trombophilia with severe thrombogenic features. Pregnancies accompanying protein S deficiency often result in loss of fetus. In this paper, we present the case of a protein S deficiency patient who eventually had a live birth despite the cerebral sinus thrombosis in the 30th week of her pregnancy and discuss the case with references to the relevant literature.

Hereditary thrombophylic mutations are seen in 10% of the general population and many cases are diagnosed as a result of complications that occur during pregnancy. Of these, Protein S deficiency is a rare hereditary trombophilia with severe thrombogenic features. Pregnancies accompanying protein S deficiency often result in loss of fetus. In this paper, we present the case of a protein S deficiency patient who eventually had a live birth despite the cerebral sinus thrombosis in the 30th week of her pregnancy and discuss the case with references to the relevant literature.