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Anomalous left coronary artery from pulmonary artery (ALCAPA) in asymptomatic 11-year-old case

dc.contributor.authorKoca, Bulent
dc.contributor.authorSaltik, Levent
dc.contributor.authorEroglu, Ayse Guler
dc.date.accessioned2021-03-05T19:36:26Z
dc.date.available2021-03-05T19:36:26Z
dc.date.issued2012
dc.identifier.citationKoca B., Saltik L., Eroglu A. G. , "Anomalous left coronary artery from pulmonary artery (ALCAPA) in asymptomatic 11-year-old case", TURK PEDIATRI ARSIVI-TURKISH ARCHIVES OF PEDIATRICS, cilt.47, ss.298-301, 2012
dc.identifier.issn1306-0015
dc.identifier.othervv_1032021
dc.identifier.otherav_d00dba29-0cc1-4c13-b4b5-c6b366616aee
dc.identifier.urihttp://hdl.handle.net/20.500.12627/137557
dc.identifier.urihttps://doi.org/10.4274/tpa.619
dc.description.abstractOrigin of the left coronary artery from the pulmonary trunk [Anomalous origin of the Left Coronary Artery from the Pulmonary Artery (ALCAPA)] is a rare congenital heart defect. ALCAPA is one of the common causes of myocardial ischemia or infarction in infants and children. In this report, we present an eleven-years-old patient presenting with murmur and accompanied by echocardiographic findings of dilated cardiomyopathy and angiocardiographic investigation that revealed left coronary artery originating from the pulmonary artery. (Turk Arch Ped 2012; 47: 298-301)
dc.language.isoeng
dc.subjectTıp
dc.subjectDahili Tıp Bilimleri
dc.subjectÇocuk Sağlığı ve Hastalıkları
dc.subjectSağlık Bilimleri
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectPEDİATRİ
dc.titleAnomalous left coronary artery from pulmonary artery (ALCAPA) in asymptomatic 11-year-old case
dc.typeMakale
dc.relation.journalTURK PEDIATRI ARSIVI-TURKISH ARCHIVES OF PEDIATRICS
dc.contributor.departmentİstanbul Üniversitesi , ,
dc.identifier.volume47
dc.identifier.issue4
dc.identifier.startpage298
dc.identifier.endpage301
dc.contributor.firstauthorID22184


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