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    <title>OAR@UM Collection:</title>
    <link>https://www.um.edu.mt/library/oar/handle/123456789/4317</link>
    <description />
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        <rdf:li rdf:resource="https://www.um.edu.mt/library/oar/handle/123456789/4333" />
        <rdf:li rdf:resource="https://www.um.edu.mt/library/oar/handle/123456789/4332" />
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    <dc:date>2026-04-05T12:31:48Z</dc:date>
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  <item rdf:about="https://www.um.edu.mt/library/oar/handle/123456789/4333">
    <title>An asymptomatic 11 year child with ruptured sinus of Valsalva</title>
    <link>https://www.um.edu.mt/library/oar/handle/123456789/4333</link>
    <description>Title: An asymptomatic 11 year child with ruptured sinus of Valsalva
Authors: Abqari, Shaad; Rabbani, Zeinab; Meshram, H. S.; Gupta, A.
Abstract: Ruptured sinus of Valsalva (RSOV) is a rare lesion in a paediatric age group.&#xD;
 A right sinus of&#xD;
Valsalva aneurysm usually ruptures into the right ventricle, while aneurysms of non-coronary sinus&#xD;
do so into the right atrium.&#xD;
 RSOV usually presents in the third decade of life with congestive heart&#xD;
failure and is more common among Asians with male predominance.&#xD;
It may present as acute&#xD;
cardiogenic shock and sudden death or may remain completely asymptomatic with incidental&#xD;
detection by a murmur. Surgery is indicated as early as possible, once the diagnosis is made as&#xD;
without surgery, most cases will eventually succumb to uncontrollable congestive heart failure.&#xD;
This article reports an 11 year old child with the diagnosis of ruptured sinus of Valsalva.</description>
    <dc:date>2015-01-01T00:00:00Z</dc:date>
  </item>
  <item rdf:about="https://www.um.edu.mt/library/oar/handle/123456789/4332">
    <title>Tetralogy of Fallot with absent pulmonary valve syndrome : an imaging challenge</title>
    <link>https://www.um.edu.mt/library/oar/handle/123456789/4332</link>
    <description>Title: Tetralogy of Fallot with absent pulmonary valve syndrome : an imaging challenge
Authors: Keivanidou, Anastasia; Gogou, Maria; Giannopoulos, Andreas
Abstract: Congenital absence of pulmonary valve syndrome (APV) represents a fascinating and unique&#xD;
variant of congenital heart disease. It was Chever in 1847 who first described this unique structural&#xD;
heart defect. The anatomic features consist of an incompletely formed, rudimentary pulmonary&#xD;
valve that is both stenotic and regurgitant, massively dilated pulmonary arteries and a large&#xD;
malaligned outlet ventricular septal defect. There is an association of this defect with Tetralogy of&#xD;
Fallot (ToF) due to which this condition is often referred to as Tetralogy of Fallot/absent pulmonary&#xD;
valve syndrome. Another characteristic feature is that there is virtually always absence of a patent&#xD;
ductus arteriosus. That has been hypothesized as being responsible for the pathogenesis of&#xD;
pulmonary artery dysplasia.</description>
    <dc:date>2015-01-01T00:00:00Z</dc:date>
  </item>
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