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    <link>https://www.um.edu.mt/library/oar/handle/123456789/27540</link>
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    <pubDate>Sat, 11 Apr 2026 07:17:33 GMT</pubDate>
    <dc:date>2026-04-11T07:17:33Z</dc:date>
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      <title>Dysphagia in an adult tetralogy of fallot with double aortic arch</title>
      <link>https://www.um.edu.mt/library/oar/handle/123456789/4302</link>
      <description>Title: Dysphagia in an adult tetralogy of fallot with double aortic arch
Authors: Pankaj, Bhatiya; Munesh, Tomar; Bhan, Anil
Abstract: Double aortic arch (DAA) is a common vascular ring. It may occur in isolation or coexist with&#xD;
various types of congenital heart disease . The anomaly usually presents in early infancy. This&#xD;
reports a 23yr old male presenting with dysphagia, who was found to have a double aortic arch and&#xD;
tetralogy of Fallot .Both lesions were successfully corrected surgically.</description>
      <pubDate>Tue, 01 Jan 2013 00:00:00 GMT</pubDate>
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      <dc:date>2013-01-01T00:00:00Z</dc:date>
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      <title>Primitive hepatic venous plexus in a child with scimitar syndrome and pulmonary sequestration</title>
      <link>https://www.um.edu.mt/library/oar/handle/123456789/4294</link>
      <description>Title: Primitive hepatic venous plexus in a child with scimitar syndrome and pulmonary sequestration
Authors: Morrison, M.L.; Sands, Andrew John; Paterson, Annie
Abstract: This article reports a case of scimitar syndrome with pulmonary sequestration, persistent primitive hepatic&#xD;
venous plexus and stenosis of the inferior vena cava in a child presenting with failure to thrive.&#xD;
Such associations are rare but may have implications when planning interventions for patients with&#xD;
complex congenital heart disease</description>
      <pubDate>Tue, 01 Jan 2013 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">https://www.um.edu.mt/library/oar/handle/123456789/4294</guid>
      <dc:date>2013-01-01T00:00:00Z</dc:date>
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