Ischemic Stroke in a Young Man With Mthfr A1298c and Ace I/D Polymorphism
| dc.authorscopusid | 56286078700 | |
| dc.authorscopusid | 37087441500 | |
| dc.authorscopusid | 35564273500 | |
| dc.contributor.author | Çilingir, V. | |
| dc.contributor.author | Milanlioǧlu, A. | |
| dc.contributor.author | Tombul, T. | |
| dc.date.accessioned | 2025-05-10T17:00:01Z | |
| dc.date.available | 2025-05-10T17:00:01Z | |
| dc.date.issued | 2014 | |
| dc.department | T.C. Van Yüzüncü Yıl Üniversitesi | en_US |
| dc.department-temp | Çilingir V., Yüzüncüyil University, Faculty of Medicine, Department of Neurology, Van, Turkey; Milanlioǧlu A., Yüzüncüyil University, Faculty of Medicine, Department of Neurology, Van, Turkey; Tombul T., Yüzüncüyil University, Faculty of Medicine, Department of Neurology, Van, Turkey | en_US |
| dc.description.abstract | Ischemic stroke is a leading cause of death and disability worldwide. Mutations in several candidate genes involving angiotensin-converting enzyme (ACE) and methylenetetrahydrofolate reductase (MTHFR) gene have been found to be associated with ischemic stroke. This report describes the case of a 29 year-old man who presented with sudden onset left hemiparesis and hemihipoestesia. Magnetic resonance imaging investigations showed acute ischemic infarct in the right parietal region. Mutation analysis revealed homozygout MTHFR A1298C and ACE I/D polymorphisms and laboratory invastigations showed mild hyperhomocysteinemia. No other risk factor was detected for ischemic stroke etiology. | en_US |
| dc.identifier.doi | 10.5505/tbdhd.2014.96658 | |
| dc.identifier.endpage | 76 | en_US |
| dc.identifier.issn | 1301-1375 | |
| dc.identifier.issue | 2 | en_US |
| dc.identifier.scopus | 2-s2.0-84907370128 | |
| dc.identifier.scopusquality | N/A | |
| dc.identifier.startpage | 73 | en_US |
| dc.identifier.uri | https://doi.org/10.5505/tbdhd.2014.96658 | |
| dc.identifier.uri | https://hdl.handle.net/20.500.14720/4838 | |
| dc.identifier.volume | 20 | en_US |
| dc.identifier.wosquality | N/A | |
| dc.language.iso | en | en_US |
| dc.publisher | Turkish Society of Cerebrovascular Diseases | en_US |
| dc.relation.ispartof | Turk Serebrovaskuler Hastaliklar Dergisi | en_US |
| dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
| dc.rights | info:eu-repo/semantics/openAccess | en_US |
| dc.subject | Ace I/D Polymorphism | en_US |
| dc.subject | Etiology | en_US |
| dc.subject | Genetic Etiology | en_US |
| dc.subject | Genetic Polymorphism | en_US |
| dc.subject | Ischemic Stroke | en_US |
| dc.subject | Mthfr A1298C Polymorphism | en_US |
| dc.title | Ischemic Stroke in a Young Man With Mthfr A1298c and Ace I/D Polymorphism | en_US |
| dc.type | Article | en_US |