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  <title>OAR@UM Collection:</title>
  <link rel="alternate" href="https://www.um.edu.mt/library/oar/handle/123456789/3658" />
  <subtitle />
  <id>https://www.um.edu.mt/library/oar/handle/123456789/3658</id>
  <updated>2026-04-19T18:35:49Z</updated>
  <dc:date>2026-04-19T18:35:49Z</dc:date>
  <entry>
    <title>Dysphagia in an adult tetralogy of fallot with double aortic arch</title>
    <link rel="alternate" href="https://www.um.edu.mt/library/oar/handle/123456789/4302" />
    <author>
      <name>Pankaj, Bhatiya</name>
    </author>
    <author>
      <name>Munesh, Tomar</name>
    </author>
    <author>
      <name>Bhan, Anil</name>
    </author>
    <id>https://www.um.edu.mt/library/oar/handle/123456789/4302</id>
    <updated>2018-02-14T12:42:11Z</updated>
    <published>2013-01-01T00:00:00Z</published>
    <summary type="text">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.</summary>
    <dc:date>2013-01-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Primitive hepatic venous plexus in a child with scimitar syndrome and pulmonary sequestration</title>
    <link rel="alternate" href="https://www.um.edu.mt/library/oar/handle/123456789/4294" />
    <author>
      <name>Morrison, M.L.</name>
    </author>
    <author>
      <name>Sands, Andrew John</name>
    </author>
    <author>
      <name>Paterson, Annie</name>
    </author>
    <id>https://www.um.edu.mt/library/oar/handle/123456789/4294</id>
    <updated>2019-07-17T09:13:58Z</updated>
    <published>2013-01-01T00:00:00Z</published>
    <summary type="text">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</summary>
    <dc:date>2013-01-01T00:00:00Z</dc:date>
  </entry>
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