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Postductal Origin of the Left Carotid, Left Subclavian, and Aberrant Retroesophageal Right Innominate Arteries in Truncus Arteriosus with Interrupted Aortic Arch
dc.contributor.authorAllen, S. W.en_US
dc.contributor.authorStrouse, Peter J.en_US
dc.contributor.authorIshizaka, T.en_US
dc.contributor.authorOhye, Richard G.en_US
dc.date.accessioned2006-09-11T19:46:23Z
dc.date.available2006-09-11T19:46:23Z
dc.date.issued2003-12en_US
dc.identifier.citationIshizaka, T.; Allen, S. W.; Strouse, P. J.; Ohye, R. G.; (2003). "Postductal Origin of the Left Carotid, Left Subclavian, and Aberrant Retroesophageal Right Innominate Arteries in Truncus Arteriosus with Interrupted Aortic Arch." Pediatric Cardiology 24(6): 581-584. <http://hdl.handle.net/2027.42/48102>en_US
dc.identifier.issn1432-1971en_US
dc.identifier.issn0172-0643en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/48102
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=12881772&dopt=citationen_US
dc.description.abstractA neonate presented to the C.S. Mott Children’s Hospital at the University of Michigan with truncus arteriosus and interrupted left aortic arch, with associated postductal origin of the left carotid, left subclavian, and aberrant retroesophageal right innominate arteries. In addition, the patient was diagnosed with DiGeorge syndrome. This unique anomaly has not been previously reported. The anatomy, pathophysiology, embryology, and successful surgical management of this anomaly are reviewed in this report.en_US
dc.format.extent191643 bytes
dc.format.extent3115 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherSpringer-Verlagen_US
dc.subject.otherPhilosophyen_US
dc.subject.otherCongenital Heart Diseaseen_US
dc.subject.otherInterrupted Aortic Archen_US
dc.subject.otherTruncus Arteriosusen_US
dc.titlePostductal Origin of the Left Carotid, Left Subclavian, and Aberrant Retroesophageal Right Innominate Arteries in Truncus Arteriosus with Interrupted Aortic Archen_US
dc.typeArticleen_US
dc.subject.hlbsecondlevelPublic Healthen_US
dc.subject.hlbsecondlevelPediatricsen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDivision of Pediatric Cardiovascular Surgery, Section of Cardiac Surgery, C.S. Mott Children’s Hospital, University of Michigan Health System, Ann Arbor, MI 48109, USAen_US
dc.contributor.affiliationumSection of Pediatric Radiology, C.S. Mott Children’s Hospital, University of Michigan Health System, Ann Arbor, MI 48109, USAen_US
dc.contributor.affiliationumDivision of Pediatric Cardiovascular Surgery, Section of Cardiac Surgery, C.S. Mott Children’s Hospital, University of Michigan Health System, Ann Arbor, MI 48109, USAen_US
dc.contributor.affiliationotherPediatric Cardiology, The Wichita Clinic, Wichita, KS, USAen_US
dc.contributor.affiliationumcampusAnn Arboren_US
dc.identifier.pmid12881772en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/48102/1/246_2003_Article_475.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1007/s00246-003-0475-6en_US
dc.identifier.sourcePediatric Cardiologyen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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