Please use this identifier to cite or link to this item: https://www.um.edu.mt/library/oar/handle/123456789/4302
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dc.contributor.authorPankaj, Bhatiya
dc.contributor.authorMunesh, Tomar
dc.contributor.authorBhan, Anil
dc.date.accessioned2015-07-27T08:44:31Z
dc.date.available2015-07-27T08:44:31Z
dc.date.issued2013
dc.identifier.citationImages in Paediatric Cardiology. 2013, Vol.15(3) p. 6-13en_GB
dc.identifier.urihttps://www.um.edu.mt/library/oar//handle/123456789/4302
dc.description.abstractDouble aortic arch (DAA) is a common vascular ring. It may occur in isolation or coexist with various types of congenital heart disease . The anomaly usually presents in early infancy. This reports a 23yr old male presenting with dysphagia, who was found to have a double aortic arch and tetralogy of Fallot .Both lesions were successfully corrected surgically.en_GB
dc.language.isoenen_GB
dc.publisherImages in Paediatric Cardiologyen_GB
dc.rightsinfo:eu-repo/semantics/openAccessen_GB
dc.subjectAortaen_GB
dc.subjectDeglutition disordersen_GB
dc.subjectTetralogy of Falloten_GB
dc.titleDysphagia in an adult tetralogy of fallot with double aortic archen_GB
dc.typearticleen_GB
dc.rights.holderThe copyright of this work belongs to the author(s)/publisher. The rights of this work are as defined by the appropriate Copyright Legislation or as modified by any successive legislation. Users may access this work and can make use of the information contained in accordance with the Copyright Legislation provided that the author must be properly acknowledged. Further distribution or reproduction in any format is prohibited without the prior permission of the copyright holder.en_GB
dc.description.reviewedpeer-revieweden_GB
Appears in Collections:IPC, Volume 15, Issue 3
IPC, Volume 15, Issue 3

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