Multiple thromboses at multiple sites A known hereditary disease emerging late but suddenly and extensively

Ozcan, F.Sen, N.Turak, O.Okten, S.Ozlu, M. F.2024-09-182024-09-1820120340-9937https://doi.org/10.1007/s00059-011-3565-xhttps://hdl.handle.net/20.500.12483/10597Hyperhomocysteinemia is a significant independent, usually heritable, prothrombotic risk factor for atherothrombotic cardiovascular, cerebrovascular, and peripheral vascular disease. We report a 42-year-old woman who had multiple embolic events.eninfo:eu-repo/semantics/closedAccessHyperhomocysteinemiaMethylenetetrahydrofolate reductase gene mutationMyocardial infarctionHypercoagulabilityThrombolytic therapyMultiple thromboses at multiple sites A known hereditary disease emerging late but suddenly and extensivelyArticle37445345510.1007/s00059-011-3565-x221939482-s2.0-84864253500Q3WOS:000305737700013Q4