Mobile right heart thrombus as a manifestation of homozygous mutation of MTHFR 1298 A > C
Yükleniyor...
Dosyalar
Tarih
2012
Dergi Başlığı
Dergi ISSN
Cilt Başlığı
Yayıncı
Turkish Soc Cardiology
Erişim Hakkı
info:eu-repo/semantics/openAccess
Özet
Mobile right heart thrombus (MRHT) is uncommon pathology but the true prevalence is still unknown. Previous studies reported that MRHT occurs in 7% to 18% of patients with pulmonary embolism with high mortality rate (44.7%) (1). The main manifestations of venous thromboembolism (VTE) are deep venous thrombosis (DVT) and pulmonary embolism. In addition, genetic factors play an important role in pathogenesis of VTE. The relationship between common genetic mutations such as factor V Leiden, prothrombin factor II G 20210A, methylenetetrahydrofolate reductase (MTHFR), deficiencies of protein C, protein S, and antithrombin III, and VTE have been reported (2).
Açıklama
Anahtar Kelimeler
Kaynak
Anatolian Journal of Cardiology
WoS Q Değeri
N/A
Scopus Q Değeri
Q3
Cilt
12
Sayı
6
Künye
Gül, E. E., Erdoğan, H. İ., Bayram, U. T., Özdemir, K., Taşçı, İ., (2012). Mobile Right Heart Thrombus as a
Manifestation of Homozygous Mutation of Mthfr 1298 a>c. Anatolian Journal of Cardiology, 12(6), 527-528. Doi:10.5152/akd.2012.167
