Recurrent Acute Coronary Syndromes With Normal Homocystein Level: A Mutation of MTHFR Gene

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dc.contributor.authorGurel, Ozgul Malcok
dc.contributor.authorDemircelik, Muhammed Bora
dc.contributor.authorGunes, Mahmut
dc.contributor.authorEryonucu, Beyhan
dc.date.accessioned2025-10-24T18:09:35Z
dc.date.available2025-10-24T18:09:35Z
dc.date.issued2014
dc.departmentMalatya Turgut Özal Üniversitesi
dc.description.abstractA 29-year-old female patient, complaining of squeezing retrosternal chest pain, was admitted to our emergency department. Her angina pectoris had started fifteen days ago and accentuated during the last two days. In her medical history, it was determined that during the last four years she had been admitted to hospitals with the same complaint twice, troponins were found to be elevated, she was hospitalized and coronary angiography (CAG) was totally normal. The young woman with recurrent acute coronary syndrome had a mutation in the MTHFR gene. On the determination of normal coronary arteries, we have demonstrated the localization of myocardial infarction via magnetic resonance imaging. In our case we have found no other risk factors except MTHFR 1298 gene mutation for coronary artery disease. MTHFR 1298 gene mutation may cause this state of hypercoagulopathy.
dc.identifier.doi10.12996/gmj.2014.09
dc.identifier.endpage36
dc.identifier.issn2147-2092
dc.identifier.issue1
dc.identifier.scopus2-s2.0-84940276256
dc.identifier.scopusqualityQ4
dc.identifier.startpage35
dc.identifier.trdizinid166030
dc.identifier.urihttps://doi.org/10.12996/gmj.2014.09
dc.identifier.urihttps://search.trdizin.gov.tr/tr/yayin/detay/166030
dc.identifier.urihttps://hdl.handle.net/20.500.12899/3717
dc.identifier.volume25
dc.identifier.wosWOS:000217468400009
dc.identifier.wosqualityN/A
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakTR
dc.language.isoen
dc.publisherGazi Univ, Fac Med
dc.relation.ispartofGazi Medical Journal
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/openAccess
dc.snmzKA_20251023
dc.subjectAcute coronary syndrome; cardiac emboli; heterozygous mutation of MTHFR A1298C gene; young patient
dc.titleRecurrent Acute Coronary Syndromes With Normal Homocystein Level: A Mutation of MTHFR Gene
dc.typeArticle

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