Double aortic arch with mirror-image dextrocardia [Ayna hayali dekstrokardi ile birlikte çift arkus aorta]

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dc.contributor.authorAltın, Hakan
dc.contributor.authorAlp, Hayrullah
dc.contributor.authorŞap, Fatih
dc.contributor.authorKarataş, Zehra
dc.contributor.authorBaysal, Tamer
dc.contributor.authorKaraaslan, Sevim
dc.date.accessioned2020-03-26T18:44:38Z
dc.date.available2020-03-26T18:44:38Z
dc.date.issued2013
dc.departmentSelçuk Üniversitesien_US
dc.description.abstractDouble aortic arch (DAA) is a very rare congenital vascular anomaly, characterized by the encircling trachea and esophagus, resulting feeding and/or respiratory problems. In this article, a two-month-old girl with situs inversus totalis and DAA was presented. The baby was symptomatic with noisy breathing and coughing since birth. Double aortic arch was detected by echocardiography, barium esophagography, cardiac MRI and conventional angiography. The present report emphasis that vascular ring should have been evaluated in a patient with respiratory and/or feeding problems. Chest radiography, barium esophagography, echocardiography, multislice computed tomography, magnetic resonance imaging angiography and conventional cardiovascular angiography can be used for the diagnosis of DAA.en_US
dc.identifier.endpage76en_US
dc.identifier.issn1304-3889en_US
dc.identifier.issueSUPPL.1en_US
dc.identifier.scopusqualityN/Aen_US
dc.identifier.startpage72en_US
dc.identifier.urihttps://hdl.handle.net/20.500.12395/30026
dc.identifier.volume10en_US
dc.indekslendigikaynakScopusen_US
dc.language.isoenen_US
dc.relation.ispartofEuropean Journal of General Medicineen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.selcuk20240510_oaigen_US
dc.subjectDextrocardiaen_US
dc.subjectDouble aortic archen_US
dc.subjectVascular ringen_US
dc.titleDouble aortic arch with mirror-image dextrocardia [Ayna hayali dekstrokardi ile birlikte çift arkus aorta]en_US
dc.typeArticleen_US

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