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CASE REPORT
Year : 2020  |  Volume : 30  |  Issue : 3  |  Page : 162-164

Isolated double-chambered right ventricle – A rare entity


1 Department of Preventive and Noninvasive Cardiology, Jaipur Heart Institute, Jaipur, Rajasthan, India
2 Department of Cardiology, Jaipur Heart Institute, Jaipur, Rajasthan, India

Correspondence Address:
Deepak Agrawal
301, Sangam Residency, Opposite Kartarpura Phatak, Vijay Nagar, Jaipur - 302 006, Rajasthan
India
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/jcecho.jcecho_36_20

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A double-chambered right ventricle (DCRV) is a rare congenital heart disease and an uncommon cause of congestive heart failure. An anomalous muscle band divides the right ventricle into two cavities: the proximal high-pressure chamber and the distal low-pressure chamber. Most cases are diagnosed and treated during childhood. Furthermore, there is a tendency for progression, if not treated early. Echocardiography is considered useful for the diagnosis of this ailment. Most of the patients have associated congenital anomalies, such as ventricular septal defect, pulmonary stenosis, and subaortic stenosis. Isolated DCRV is a rare entity. Hence, we report a case of an isolated DCRV in an adult patient.


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