Myocardial infarction and venous thrombosis in a 42-year old woman with heterozygous methylenetetrahydrofolate reductase (MTHRF) gene mutation, hyperhomocysteinemia, and protein C deficiency
dc.contributor.author | Çakır, Ömer | |
dc.contributor.author | Ayyıldız, Orhan | |
dc.contributor.author | Göz, Mustafa | |
dc.contributor.author | Şit, Dede | |
dc.contributor.author | Eren, Nesimi | |
dc.date.accessioned | 2024-04-24T17:56:08Z | |
dc.date.available | 2024-04-24T17:56:08Z | |
dc.date.issued | 2007 | |
dc.department | Dicle Üniversitesi, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü, İç Hastalıkları Ana Bilim Dalı | en_US |
dc.description.abstract | Objective: Hyperhomocysteinemia and protein C deficiency have synergistic effect on the onset of thrombotic disease. Methods: We report a 42-year old woman with myocardial infarction and venous thrombosis in whom recognition of heterozygous MTHRF gene mutation, hyperhomocysteinemia, and protein C deficiency. Results: The patient was treated successfully with coronary artery bypass graft surgery and systemic anticoagulation. Conclusions: Our report emphasize that a combined hyperhomocysteinemia, and protein C deficiency may be a high risk factor for arterial and venous thromboembolic events in young adults. These patients might be candidates for indefinite anticoagulation. | en_US |
dc.identifier.citation | Çakır, Ö., Ayyıldız, O., Göz, M., Şit, D. ve Eren, N. (2007). Myocardial infarction and venous thrombosis in a 42-year old woman with heterozygous methylenetetrahydrofolate reductase (MTHRF) gene mutation, hyperhomocysteinemia, and protein C deficiency. International Journal of Cardiology, 117(3), e98-e100. | |
dc.identifier.doi | 10.1016/j.ijcard.2006.11.204 | |
dc.identifier.endpage | e100 | en_US |
dc.identifier.issn | 0167-5273 | |
dc.identifier.issue | 3 | en_US |
dc.identifier.pmid | 17360059 | en_US |
dc.identifier.scopus | 2-s2.0-33947716365 | en_US |
dc.identifier.scopusquality | Q1 | en_US |
dc.identifier.startpage | e98 | en_US |
dc.identifier.uri | https://doi.org/10.1016/j.ijcard.2006.11.204 | |
dc.identifier.uri | https://hdl.handle.net/11468/23313 | |
dc.identifier.uri | https://www.sciencedirect.com/science/article/pii/S0167527307002288?via%3Dihub | |
dc.identifier.volume | 117 | en_US |
dc.indekslendigikaynak | Scopus | en_US |
dc.indekslendigikaynak | PubMed | en_US |
dc.institutionauthor | Ayyıldız, Orhan | |
dc.language.iso | en | en_US |
dc.relation.ispartof | International Journal of Cardiology | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | Hyperhomocysteinemia | en_US |
dc.subject | Mthrf gene mutation | en_US |
dc.subject | Protein C deficiency | en_US |
dc.title | Myocardial infarction and venous thrombosis in a 42-year old woman with heterozygous methylenetetrahydrofolate reductase (MTHRF) gene mutation, hyperhomocysteinemia, and protein C deficiency | en_US |
dc.type | Article | en_US |
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