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dc.contributor.authorGüdücü, Nilgün
dc.contributor.authorKutay, Salih Serdar
dc.contributor.authorÖzenç, Ebru
dc.contributor.authorÇiftçi, Çavlan
dc.contributor.authorBaşgül Yiğiter, Alin
dc.contributor.authorİşçi, Herman
dc.date.accessioned2014-12-29T14:50:35Z
dc.date.available2014-12-29T14:50:35Z
dc.date.issued2011
dc.identifier.citationGuducu N, Kutay SS, Ozenc E, Ciftci C, Yigiter AB, Isci H. Management of a rare case of arrhythmogenic right ventricular dysplasia in pregnancy: a case report. Journal of Medical Case Reports. 2011; 5: 300. doi: 10.1186/1752-1947-5-300.en_US
dc.identifier.issn1752-1947en_US
dc.identifier.urihttp://www.jmedicalcasereports.com/content/5/1/300en_US
dc.identifier.urihttps://hdl.handle.net/11446/638en_US
dc.descriptionİstanbul Bilim Üniversitesi, Tıp Fakültesi.en_US
dc.description.abstractArrhythmogenic right ventricular dysplasia is a heritable disease of the heart muscle characterized by fibrofatty degeneration of cardiomyocytes. Patients present with ventricular arrhythmias or congestive heart failure, and sometimes sudden cardiac death occurs. Prenatal diagnosis has become possible with the detection of mutations, but, to the best of our knowledge, no case of prenatal diagnosis has been reported previously. There is little information about the management of arrhythmogenic right ventricular dysplasia in pregnancy, and the preferred mode of delivery is not certain; therefore, we present the case of a patient with arrhythmogenic right ventricular dysplasia and discuss the prenatal diagnosis, patient management and prognosis in pregnancy.en_US
dc.language.isoengen_US
dc.publisherBioMed Centralen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.titleManagement of a rare case of arrhythmogenic right ventricular dysplasia in pregnancy: a case reporten_US
dc.typereporten_US
dc.relation.journalJournal of Medical Case Reportsen_US
dc.departmentDBÜ, Tıp Fakültesien_US
dc.identifier.volume5
dc.contributor.authorIDTR123126en_US
dc.contributor.authorIDTR143675en_US
dc.contributor.authorIDTR115014en_US
dc.contributor.authorIDTR122849en_US
dc.contributor.authorIDTR123093en_US
dc.relation.publicationcategoryDiğeren_US


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