Publication:
Cor trıatrıatum assocıated wıth ebsteın malformatıon of atretıc mıtral valve and double outlet rıght ventrıcle

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dc.contributor.authorÖztunç, Funda
dc.contributor.authorAkalın, Figen
dc.contributor.authorBeşikçi, Resmiye
dc.contributor.authorIDTR175423en_US
dc.contributor.authorIDTR188943en_US
dc.contributor.departmentSub-department of Pediatric Cardiology, Department of Pediatrics, School of Medicine, Marmara University, Istanbul, Turkeyen_US
dc.date.accessioned2016-06-10T14:36:33Z
dc.date.accessioned2026-01-11T14:31:31Z
dc.date.available2016-06-10T14:36:33Z
dc.date.issued2000
dc.description.abstractCor triatriatum is a rare congenital cardiac anomaly and association of this pathology with Ebstein's malformation of atretic mitral valve and double outlet right ventricle has not been previously reported. We present an 11-day-old infant with this unique anomaly diagnosed by echocardiographic examination. The infant died before surgical intervention.en_US
dc.identifier.endpage225en_US
dc.identifier.issue4en_US
dc.identifier.startpage223en_US
dc.identifier.urihttps://hdl.handle.net/11424/4662
dc.identifier.volume13en_US
dc.language.isoengen_US
dc.relation.journalMarmara Medicial Journalen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectCor triatriatum, Ebstein anomaly, Mitral valve atresia, Double outlet right ventricleen_US
dc.titleCor trıatrıatum assocıated wıth ebsteın malformatıon of atretıc mıtral valve and double outlet rıght ventrıcleen_US
dc.typearticleen_US
dspace.entity.typePublication

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