Anomalous Origin of the Left Coronary Artery from the Pulmonary Artery (ALCAPA) in an Adult

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dc.contributor.authorNazli, Yunus
dc.contributor.authorAksoy, Omer Nuri
dc.contributor.authorKorkmaz, Kemal
dc.contributor.authorAkkaya, Ismail Olgun
dc.contributor.authorColak, Necmettin
dc.date.accessioned2025-10-24T18:10:00Z
dc.date.available2025-10-24T18:10:00Z
dc.date.issued2013
dc.departmentMalatya Turgut Özal Üniversitesi
dc.description.abstractAnomalous origin of the left main coronary artery from the pulmonary artery (ALCAPA), also known as Garland-Bland-White syndrome, is an extremely rare but potentially fatal congenital cardiovascular anomaly and it often exists as an isolated condition. We report an unusual case of a 32 years-old patient with ALCAPA presenting with chest pain and dyspnea who underwent surgical correction of this rare anomaly. This anomaly was simply repaired by the combination of LMCA ligation and coronary artery bypass grafting.
dc.identifier.doi10.4328/JCAM.2501
dc.identifier.endpage448
dc.identifier.issn1309-0720
dc.identifier.issn1309-2014
dc.identifier.startpage446
dc.identifier.urihttps://doi.org/10.4328/JCAM.2501
dc.identifier.urihttps://hdl.handle.net/20.500.12899/3938
dc.identifier.volume4
dc.identifier.wosWOS:000215555000036
dc.identifier.wosqualityN/A
dc.indekslendigikaynakWeb of Science
dc.language.isotr
dc.publisherDerman Medical Publ
dc.relation.ispartofJournal Of Clinical And Analytical Medicine
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/openAccess
dc.snmzKA_20251023
dc.subjectCongenital Heart Defect; Coronary Artery Bypass Grafting
dc.titleAnomalous Origin of the Left Coronary Artery from the Pulmonary Artery (ALCAPA) in an Adult
dc.typeArticle

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