Publication:
Both coronary arteries originating from the pulmonary artery: A case report [Her iki koroner arterin pulmoner arterden köken almasi: Bir vaka takdimi]

dc.contributor.authorsAkalin F., Topçu B.
dc.date.accessioned2022-03-28T14:56:36Z
dc.date.accessioned2026-01-10T19:10:53Z
dc.date.available2022-03-28T14:56:36Z
dc.date.issued2009
dc.description.abstractBoth coronary arteries originating from the pulmonary artery is an extremely rare potentially fatal condition reported in only a few cases, causing dilated cardiomyopathy in early infancy. We report a three-month-old patient presenting with cardiomegaly and heart failure accompanied by echocardiographic findings of dilated cardiomyopathy and both coronary arteries originating from the pulmonary artery.
dc.identifier.issn100161
dc.identifier.pubmedCSHDA
dc.identifier.urihttps://hdl.handle.net/11424/256372
dc.language.isotur
dc.relation.ispartofCocuk Sagligi ve Hastaliklari Dergisi
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectALCAPA
dc.subjectCoronary artery abnormality
dc.subjectDilated cardiomyopathy
dc.titleBoth coronary arteries originating from the pulmonary artery: A case report [Her iki koroner arterin pulmoner arterden köken almasi: Bir vaka takdimi]
dc.typearticle
dspace.entity.typePublication
oaire.citation.endPage84
oaire.citation.issue2
oaire.citation.startPage81
oaire.citation.titleCocuk Sagligi ve Hastaliklari Dergisi
oaire.citation.volume52

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