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- W2340023365 endingPage "489" @default.
- W2340023365 startingPage "481" @default.
- W2340023365 abstract "Distribution of hereditary thrombophilic gene mutations differs globally. Prothrombin gene mutation G20210A is a common prothrombotic single-nucleotide polymorphism. In this systematic review, we provide a comprehensive report of the prevalence of prothrombin G20210A across the globe. Databases [Pubmed, Web of Science, Embase] were interrogated from their inception through December 2015 for articles reporting prothrombin G20210A prevalence rates and ethnicity. Prevalence rates were organized by continent and ethnoracial ancestry. A total of 113 articles were included with a total 61 876 participants tested for prothrombin G20210A. Reported prevalence rates varied from 0 to 15.9% among ethnic groups, with higher rates seen in the thromboembolism affected cohort compared with the unaffected cohort. Carrier rate distribution is supported by known historical migration patterns of global populations. This review of prothrombin G20210A prevalence may guide resourceful screening for identification of hereditary thrombophilia in female populations of interest with hypercoagulable states." @default.
- W2340023365 created "2016-06-24" @default.
- W2340023365 creator A5011998743 @default.
- W2340023365 creator A5024703876 @default.
- W2340023365 date "2016-07-01" @default.
- W2340023365 modified "2023-10-16" @default.
- W2340023365 title "Global prevalence of prothrombin gene mutation G20210A and implications in women's health" @default.
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