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  <title>OAR@UM Collection:</title>
  <link rel="alternate" href="https://www.um.edu.mt/library/oar/handle/123456789/4317" />
  <subtitle />
  <id>https://www.um.edu.mt/library/oar/handle/123456789/4317</id>
  <updated>2026-06-12T10:43:10Z</updated>
  <dc:date>2026-06-12T10:43:10Z</dc:date>
  <entry>
    <title>An asymptomatic 11 year child with ruptured sinus of Valsalva</title>
    <link rel="alternate" href="https://www.um.edu.mt/library/oar/handle/123456789/4333" />
    <author>
      <name>Abqari, Shaad</name>
    </author>
    <author>
      <name>Rabbani, Zeinab</name>
    </author>
    <author>
      <name>Meshram, H. S.</name>
    </author>
    <author>
      <name>Gupta, A.</name>
    </author>
    <id>https://www.um.edu.mt/library/oar/handle/123456789/4333</id>
    <updated>2020-03-25T14:29:46Z</updated>
    <published>2015-01-01T00:00:00Z</published>
    <summary type="text">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.</summary>
    <dc:date>2015-01-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Tetralogy of Fallot with absent pulmonary valve syndrome : an imaging challenge</title>
    <link rel="alternate" href="https://www.um.edu.mt/library/oar/handle/123456789/4332" />
    <author>
      <name>Keivanidou, Anastasia</name>
    </author>
    <author>
      <name>Gogou, Maria</name>
    </author>
    <author>
      <name>Giannopoulos, Andreas</name>
    </author>
    <id>https://www.um.edu.mt/library/oar/handle/123456789/4332</id>
    <updated>2017-11-29T15:37:25Z</updated>
    <published>2015-01-01T00:00:00Z</published>
    <summary type="text">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.</summary>
    <dc:date>2015-01-01T00:00:00Z</dc:date>
  </entry>
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