2012
DOI: 10.1002/jcu.21979
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A case of asymptomatic isolated double‐chambered right ventricle in an adult man

Abstract: Double-chambered right ventricle is a rare congenital heart disease. An anomalous muscle band divides the right ventricle into two cavities, causing a variable degree of obstruction. Most cases of double-chambered right ventricle are diagnosed and treated during childhood, whereas cases of initial presentation during adulthood are very rare. We report a case of asymptomatic isolated double-chambered right ventricle incidentally found in an adult man.

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Cited by 3 publications
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“…Most cases of DCRV are diagnosed and treated during childhood, where as an initial presentation during adulthood has been reported in rare cases [7,2,8].…”
Section: Discussionmentioning
confidence: 99%
“…Most cases of DCRV are diagnosed and treated during childhood, where as an initial presentation during adulthood has been reported in rare cases [7,2,8].…”
Section: Discussionmentioning
confidence: 99%
“…These defects result from an impaired growth of the trabecular myocardium during the early fetal formation, and the non-uniformity in its position, closer to the tricuspid or pulmonary valve, which causes the ventricle to divide into two parts – a proximal and a distal part. They are frequently associated with ventricular septal defects (80% of cases) 1 , 2 . Even when their impact is minor, these obstructive anomalies should be treated earlier to prevent an unfavorable outcome in relation to the development of myocardial fibrosis, arrhythmias and heart failure.…”
Section: Laboratory Testsmentioning
confidence: 99%