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

Yükleniyor...
Küçük Resim

Tarih

2014

Dergi Başlığı

Dergi ISSN

Cilt Başlığı

Yayıncı

İnönü Üniversitesi Tıp Fakültesi Dergisi

Erişim Hakkı

info:eu-repo/semantics/openAccess

Özet

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.

Açıklama

[Turgut Özal Tıp Merkezi Dergisi, (2014).21 (4)]

Anahtar Kelimeler

Protein S Eksikliği, Herediter Trombofilia, Serebral Sinüs Trombozu, Gebelik, Protein S Deficiency, Hereditary Thrombophilia, Cerebral Sinus Trombosis, Pregnancy

Kaynak

Turgut Özal Tıp Merkezi Dergisi

WoS Q Değeri

Scopus Q Değeri

Cilt

21

Sayı

4

Künye

Bulanık, M., Dağ, Z. Özcan.,Demiray, D.,Dağ, E.,Şimşek, Y.,(2014).Gebelite protein-s eksikliği ile ilişkili serebral sinüs trombozu: nadir bir olgu sunumu.Turgut Özal Tıp Merkezi Dergisi, 21 (4).307-309 ss.