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    <title>OAR@UM Collection:</title>
    <link>https://www.um.edu.mt/library/oar/handle/123456789/27498</link>
    <description />
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        <rdf:li rdf:resource="https://www.um.edu.mt/library/oar/handle/123456789/4068" />
        <rdf:li rdf:resource="https://www.um.edu.mt/library/oar/handle/123456789/4067" />
        <rdf:li rdf:resource="https://www.um.edu.mt/library/oar/handle/123456789/4062" />
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    <dc:date>2026-06-26T05:21:03Z</dc:date>
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  <item rdf:about="https://www.um.edu.mt/library/oar/handle/123456789/4068">
    <title>Clinical manifestations of Deletion 22q11.2 syndrome (DiGeorge/Velo-CardioFacial syndrome)</title>
    <link>https://www.um.edu.mt/library/oar/handle/123456789/4068</link>
    <description>Title: Clinical manifestations of Deletion 22q11.2 syndrome (DiGeorge/Velo-CardioFacial syndrome)
Authors: Digilio, Maria Cristina; Marino, Bonnie; Capolino, Rossella; Dallapiccola, B.
Abstract: Deletion 22q11.2 syndrome (Del22) (DiGeorge/Velo-Cardio-Facial syndrome) is&#xD;
characterized by congenital heart defect (CHD), palatal anomalies, facial&#xD;
dysmorphisms, neonatal hypocalcemia, immune deficit, speech and learning&#xD;
disabilities. CHD is present in 75% of patients with Del22. The most frequently seen&#xD;
cardiac malformations are “conotruncal” defects, including tetralogy of Fallot (TF),&#xD;
pulmonary atresia with ventricular septal defect (PA-VSD), truncus arteriosus (TA),&#xD;
interrupted aortic arch (IAA), and ventricular septal defect (VSD). The study of the&#xD;
specific “cardiac phenotype” in patients with Del22 shows that a particular cardiac&#xD;
anatomy can be identied in these subjects. In addition to CHD, various organ&#xD;
systems can be involved, so that a multidisciplinary approach is needed in the&#xD;
evaluation of patients with Del22.</description>
    <dc:date>2005-01-01T00:00:00Z</dc:date>
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  <item rdf:about="https://www.um.edu.mt/library/oar/handle/123456789/4067">
    <title>Poststenotic aneurysm in a child with native coarctation of the aortic arch</title>
    <link>https://www.um.edu.mt/library/oar/handle/123456789/4067</link>
    <description>Title: Poststenotic aneurysm in a child with native coarctation of the aortic arch
Authors: Knirsch, Walter; Schlensak, C.; Dittrich, Sven; Kurtz, Caroline; Kececioglu, Deniz
Abstract: This article contains images taken whilst diagnosing a 12-year old girl who was admitted to hospital because of arterial hypertension, emboli to lower extremities and exertional dyspnea.  The patient was operated by using a 18 mm Dacron tube prothesis.</description>
    <dc:date>2005-01-01T00:00:00Z</dc:date>
  </item>
  <item rdf:about="https://www.um.edu.mt/library/oar/handle/123456789/4062">
    <title>Cardiovascular involvement in Kawaski Disease</title>
    <link>https://www.um.edu.mt/library/oar/handle/123456789/4062</link>
    <description>Title: Cardiovascular involvement in Kawaski Disease
Authors: Chintala, Kavitha; Reddy, S.V.; Forbes, T.J.
Abstract: This article contains a case report of a 19 month old child with Kawasaki Disease who developed bilateral giant coronary artery aneurysms.</description>
    <dc:date>2005-01-01T00:00:00Z</dc:date>
  </item>
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