نتایج جستجو برای: g20210a
تعداد نتایج: 673 فیلتر نتایج به سال:
چکید ه سابقه و هدف ترومبوآمبولی وریدی یک بیماری شایع و خطرناک است. عواملی که سبب تمایل به ایجاد ترومبوز می شوند، ممکن است ارثی یا اکتسابی باشند. جهش پروترومبین g20210a که در منطقه ترجمه نشده ' 3 ژن فاکتور ii رخ می دهد، همراه با افزایش ابتلا به ترومبوز در جمعیت قفقازی دیده می شود، البته وجود این رابطه در جمعیت های دیگر هنوز مورد بحث است. سطح پروترومبین در افرادی که واریانت هتروزیگوت ژن پروتر...
OBJECTIVE/BACKGROUND Despite being an important risk factor for venous thromboembolism, the role of the prothrombin G20210A mutation in patients with arterial disease remains unclear. The aim of this review was to evaluate the association of prothrombin G20210A and lower extremity peripheral arterial disease (PAD). METHODS This was a systematic review and meta-analysis of case-control studies...
Factor V Leiden (FVLeiden) and prothrombin G20210A are the most common genetic causes of thrombophilia and established risk factors for different clinical manifestations of venous thromboembolism (VTE). This study investigated whether the clinical manifestation of VTE, the extension of deep vein thrombosis (DVT) and the presence of transient risk factors at the time of the first VTE, differed a...
It was the aim of the present study to investigate factor II levels in liver cirrhosis (LC) patients with portal vein thrombosis (PVT) carrying the heterozygous G20210A prothrombin (PT) mutation. Plasma concentrations of factor II, VII, X, V, protein C (PC) total protein S (tPS) antithrombin (AT) and D-dimers (DD) were measured in 13 LC patients with PVT heterozygous for PT G20210A, in 13 LC pa...
BACKGROUND Homozygous or double heterozygous factor V Leiden and/or prothrombin G20210A is a rare inherited thrombophilic trait. Whether individuals with this genetic background have an increased risk of recurrent venous thrombosis is uncertain. METHODS AND RESULTS A case-control design within a large cohort of families with thrombophilia was chosen to calculate the risk of recurrent venous t...
Background: There are many genetic and non-hereditary risk factors that are known to causes venous thromboembolic (VTE) disorders, Cardiovascular diseases and types of cancer. One of these is the Prothrombin G20210A mutation. Prothrombin mutation (guanine to adenine G→A) at nucleotide position 20210, which is present in the 3′ untranslated region of the prothrombin gene. Prothrombin G20210A mut...
BACKGROUND Factor V leiden and the -G20210A variant of prothrombin gene are associated to a higher risk of deep venous thrombosis. AIM To assess the frequency of factor V Leiden (G1691A) and prothrombin -G20210A alleles in patients with deep venous thrombosis (DVT) and in the general population from Spain. MATERIAL AND METHODS Factor V Leiden (g1691a) and prothrombin-g20210a alleles were ge...
Background—Homozygous or double heterozygous factor V Leiden and/or prothrombin G20210A is a rare inherited thrombophilic trait. Whether individuals with this genetic background have an increased risk of recurrent venous thrombosis is uncertain. Methods and Results—A case-control design within a large cohort of families with thrombophilia was chosen to calculate the risk of recurrent venous thr...
چکید ه سابقه و هدف ترومبوآمبولی وریدی یک بیماری شایع و خطرناک است. عواملی که سبب تمایل به ایجاد ترومبوز میشوند، ممکن است ارثی یا اکتسابی باشند. جهش پروترومبین G20210A که در منطقه ترجمه نشده ' 3 ژن فاکتور II رخ میدهد، همراه با افزایش ابتلا به ترومبوز در جمعیت قفقازی دیده میشود، البته وجود این رابطه در جمعیتهای دیگر هنوز مورد بحث است. سطح پروترومبین در افرادی که واریانت هتروزیگوت ژن پرو...
There are many genetic and acquired risk factors that are known to cause venous thromboembolic disorders (VTE). One of these is the Prothrombin G20210A mutation, which has been identified in 1996. Prothrombin G20210A mutation causes higher levels of the clotting factor prothrombin in the blood of carriers, which creates a higher tendency towards blood clotting (hypercoagulability), and therefor...
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