• Factor V Leiden (rs6025 or F5 p.R506Q) is a variant (mutated form) of human factor V (one of several substances that helps blood clot), which causes an...
    21 KB (2,524 words) - 15:37, 15 January 2024
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    hemorrhage, while some mutations (most notably factor V Leiden) predispose for thrombosis. The gene for factor V is located on the first chromosome (1q24)...
    14 KB (1,819 words) - 15:32, 9 May 2024
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    identified in 1965, while the most common abnormalities (including factor V Leiden) were described in the 1990s. The most common conditions associated...
    43 KB (5,067 words) - 17:24, 19 January 2024
  • disorder called factor V Leiden. In factor V Leiden, a G1691A nucleotide replacement results in an R506Q amino acid mutation. Factor V Leiden increases the...
    25 KB (3,112 words) - 19:03, 28 February 2024
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    with normal plasma), coagulation factor assays, antiphospholipid antibodies, D-dimer, genetic tests (e.g. factor V Leiden, prothrombin mutation G20210A)...
    61 KB (5,960 words) - 15:41, 29 April 2024
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    form is Factor V Leiden, which is responsible for more than 95% of cases. Other genetic causes include Factor V Cambridge (VThr306) and the factor V HR2 haplotype...
    11 KB (1,036 words) - 23:10, 29 January 2023
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    County, Illinois, USA Leiden scale, for measuring extreme low temperatures. Factor V Leiden is named after the city of Leiden where it was discovered...
    55 KB (5,457 words) - 22:28, 7 May 2024
  • clotting pathway mutations that increase the risk of clots include factor V Leiden. Prothrombin G20210A was identified in the 1990s. About 2% of Caucasians...
    14 KB (1,496 words) - 18:54, 12 April 2024
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    rates. Genetic factors include non-O blood type, deficiencies of antithrombin, protein C, and protein S and the mutations of factor V Leiden and prothrombin...
    144 KB (14,621 words) - 23:44, 23 January 2024
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    hormone therapy and hormonal contraceptives) Genetic thrombophilia (factor V Leiden, prothrombin mutation G20210A, protein C deficiency, protein S deficiency...
    86 KB (9,695 words) - 03:17, 26 April 2024
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    Thrombin (redirect from Factor II)
    Prothrombin G20210A is not usually accompanied by other factor mutations (i.e., the most common is factor V Leiden). The gene may be inherited heterozygous (1 pair)...
    26 KB (2,946 words) - 11:32, 24 March 2024
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    types Pheochromocytoma Livedoid vasculopathy and its association with factor V Leiden mutation FILS syndrome (polymerase ε1 mutation in a human syndrome...
    25 KB (2,547 words) - 05:54, 8 March 2024
  • Thumbnail for Virchow's triad
    triad of Virchow (/ˈfɪərkoʊ/) describes the three broad categories of factors that are thought to contribute to thrombosis. Hypercoagulability Hemodynamic...
    10 KB (707 words) - 12:59, 20 December 2023
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    (December 2017). "Laboratory assessment of Activated Protein C Resistance/Factor V-Leiden and performance characteristics of a new quantitative assay". Transfus...
    9 KB (954 words) - 04:40, 9 April 2024
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    may be appropriate to check the antithrombin, protein C, protein S, factor V Leiden, prothrombin G20210A, and antiphospholipid antibodies.[citation needed]...
    12 KB (1,438 words) - 04:01, 7 April 2024
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    clotting disorders such as protein S deficiency, protein C deficiency, or factor V Leiden are also at increased risk of thrombophlebitis. Thrombophlebitis can...
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  • hypercoagulability. Hereditary APC resistance is usually caused by the factor V Leiden mutation, whereas acquired APC resistance has been linked to antiphospholipid...
    15 KB (1,523 words) - 11:50, 24 January 2024
  • Gurgey A. (1999). "Clinical manifestations in thrombotic children with factor V Leiden mutation". Pediatr Hematol Oncol. 16 (3): 233–237. doi:10.1080/088800199277281...
    21 KB (2,455 words) - 08:10, 12 December 2023
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    autoimmune diseases such as lupus, various inherited thrombophilias such as Factor V Leiden, renal disease, multiple gestation (twins or multiple birth), and advanced...
    93 KB (10,069 words) - 22:29, 9 April 2024
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    polycythemia vera (high red blood cell counts), and is an additional risk factor for complications.[citation needed] A very small number of people report...
    11 KB (1,066 words) - 01:55, 17 March 2024
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    to pulmonary embolism Ischemic stroke Hypercoagulable states (e.g., Factor V Leiden) — can lead to deep vein thrombosis Mechanical heart valves Myocardial...
    78 KB (8,726 words) - 15:18, 29 April 2024
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    might be involved in cancer progression. A SNP in the F5 gene causes Factor V Leiden thrombophilia. rs3091244 is an example of a triallelic SNP in the CRP...
    57 KB (6,179 words) - 04:47, 27 April 2024
  • such as antiphospholipid antibodies, and congenital ones, including factor V Leiden, prothrombin mutation, proteins C and S deficiencies, and antithrombin...
    21 KB (2,228 words) - 13:37, 23 November 2023
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    vein. It most commonly affects leg veins, such as the femoral vein. Three factors are important in the formation of a blood clot within a deep vein—these...
    47 KB (4,703 words) - 20:33, 3 April 2024
  • prior thrombotic event or who were genetically coded for clot risk (factor V Leiden or prothrombin mutation). In 2001, the U.S. Food and Drug Administration...
    92 KB (11,257 words) - 03:16, 2 May 2024
  • OMIM. It can present in conjunction with protein S deficiency and factor V Leiden. It is not currently known if sticky platelet syndrome is a distinct...
    7 KB (669 words) - 10:08, 27 August 2023
  • 1997 Lay MJ, Wittwer CT. (1997) Real-time fluorescence genotyping of factor V Leiden during rapid-cycle PCR. Clin Chem. 1997 Dec;43(12):2262-7 "Universal...
    12 KB (1,448 words) - 07:05, 11 March 2024
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    such as Factor V Leiden, antiphospholipid syndrome), malignancy (such as pancreatic cancer) or metastasis, or a combination of these factors. In some...
    12 KB (1,229 words) - 22:44, 3 December 2023
  • RAD51C, XPF 1:130,000 Fabry disease GLA (Xq22.1) P 1:117,000-476,000 Factor V Leiden thrombophilia Fatal familial insomnia PRNP dominant Familial adenomatous...
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  • Thumbnail for Budd–Chiari syndrome
    Budd–Chiari syndrome. Factor V Leiden is responsible for 8% of cases. Other less common inherited disorders leading to the condition include factor II mutation...
    19 KB (2,142 words) - 02:37, 6 September 2023