Is thrombophilia a major risk factor for deep vein thrombosis of the lower extremities among Lebanese patients?
Author(s) -
Raghid Kreidy,
Noha IraniHakime
Publication year - 2009
Publication title -
vascular health and risk management
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.892
H-Index - 68
eISSN - 1178-2048
pISSN - 1176-6344
DOI - 10.2147/vhrm.s6184
Subject(s) - medicine , thrombophilia , factor v leiden , thrombosis , deep vein , methylenetetrahydrofolate reductase , risk factor , venous thrombosis , factor v , surgery , prothrombin g20210a , population , pediatrics , genotype , environmental health , biochemistry , chemistry , gene
Factor V Leiden (R506Q) mutation is the most commonly observed inherited genetic abnormality related to vein thrombosis. Lebanon has one of the highest frequencies of this mutation in the world with a prevalence of 14.4% in the general population. The aim of this study is to define risk factors including inherited genetic abnormalities among Lebanese patients with lower extremity deep vein thrombosis. We report the clinical outcome of patients with thrombophilia.
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