<?xml version="1.0" encoding="UTF-8"?>
<feed xmlns="http://www.w3.org/2005/Atom" xmlns:dc="http://purl.org/dc/elements/1.1/">
  <title>OAR@UM Collection:</title>
  <link rel="alternate" href="https://www.um.edu.mt/library/oar/handle/123456789/3645" />
  <subtitle />
  <id>https://www.um.edu.mt/library/oar/handle/123456789/3645</id>
  <updated>2026-06-25T17:18:16Z</updated>
  <dc:date>2026-06-25T17:18:16Z</dc:date>
  <entry>
    <title>Isolated Biventricular Noncompaction in an adult with severe pulmonary hypertension : an association reviewed.</title>
    <link rel="alternate" href="https://www.um.edu.mt/library/oar/handle/123456789/4270" />
    <author>
      <name>Awasthy, Neeraj</name>
    </author>
    <author>
      <name>Tomar, Munesh</name>
    </author>
    <author>
      <name>Radhakrishnan, Sitaraman</name>
    </author>
    <id>https://www.um.edu.mt/library/oar/handle/123456789/4270</id>
    <updated>2019-02-18T18:03:07Z</updated>
    <published>2012-01-01T00:00:00Z</published>
    <summary type="text">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.</summary>
    <dc:date>2012-01-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Cor triatriatum sinister with situs inversus totalis in an infant.</title>
    <link rel="alternate" href="https://www.um.edu.mt/library/oar/handle/123456789/4269" />
    <author>
      <name>Taksande, Amar M.</name>
    </author>
    <author>
      <name>Gadekar, A.</name>
    </author>
    <author>
      <name>Meshram, Sushant</name>
    </author>
    <author>
      <name>Pathak, Swanand</name>
    </author>
    <id>https://www.um.edu.mt/library/oar/handle/123456789/4269</id>
    <updated>2018-07-10T09:12:25Z</updated>
    <published>2012-01-01T00:00:00Z</published>
    <summary type="text">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</summary>
    <dc:date>2012-01-01T00:00:00Z</dc:date>
  </entry>
</feed>

