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    <title>OAR@UM Collection:</title>
    <link>https://www.um.edu.mt/library/oar/handle/123456789/27534</link>
    <description />
    <pubDate>Mon, 27 Apr 2026 10:34:54 GMT</pubDate>
    <dc:date>2026-04-27T10:34:54Z</dc:date>
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      <title>Isolated Biventricular Noncompaction in an adult with severe pulmonary hypertension : an association reviewed.</title>
      <link>https://www.um.edu.mt/library/oar/handle/123456789/4270</link>
      <description>Title: Isolated Biventricular Noncompaction in an adult with severe pulmonary hypertension : an association reviewed.
Authors: Awasthy, Neeraj; Tomar, Munesh; Radhakrishnan, Sitaraman
Abstract: Biventricular noncompaction is a recently recognized rare form of cardiomyopathy. It&#xD;
is characterized by altered structure of myocardial wall as a result of intrauterine&#xD;
arrest of compaction of the myocardial fibers in absence of coexisting congenital&#xD;
lesion. Left ventricle is the most affected site for noncompaction, but right ventricular&#xD;
involvement has been reported in a few cases. Diagnosis is made with 2-dimensional&#xD;
echocardiography or cardiac magnetic resonance imaging. While major clinical&#xD;
manifestations are heart failure, arrhythmias and embolic events,pulmonary artery&#xD;
hypertension ( PAH)has not been well elaborated in the literature. We present a 13-&#xD;
year old boy who had Biventricular noncompaction complicated by severe pulmonary&#xD;
hypertension. Pulmonary hypertension may be a consequence of increased pulmonary&#xD;
venous pressures caused by systolic and diastolic left ventricular dysfunction&#xD;
secondary to noncompaction. This article reviews the literature particularly with reference&#xD;
to PAH in the context of this case.</description>
      <pubDate>Sun, 01 Jan 2012 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">https://www.um.edu.mt/library/oar/handle/123456789/4270</guid>
      <dc:date>2012-01-01T00:00:00Z</dc:date>
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    <item>
      <title>Cor triatriatum sinister with situs inversus totalis in an infant.</title>
      <link>https://www.um.edu.mt/library/oar/handle/123456789/4269</link>
      <description>Title: Cor triatriatum sinister with situs inversus totalis in an infant.
Authors: Taksande, Amar M.; Gadekar, A.; Meshram, Sushant; Pathak, Swanand
Abstract: Cor triatriatum sinister is a rare congenital cardiac malformation characterized by a membrane in&#xD;
the left atrium which separates the left atrium into the proximal and distal chambers.Association of&#xD;
cor triatriatum is extremely rare with situs inversus totalis. This article reports a rare case of cor&#xD;
triatriatum sinister with situs inversus totalis in a 5 month old female infant</description>
      <pubDate>Sun, 01 Jan 2012 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">https://www.um.edu.mt/library/oar/handle/123456789/4269</guid>
      <dc:date>2012-01-01T00:00:00Z</dc:date>
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