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Double chambered right ventricle is a rare cardiac defect characterised by an obstructive hypertrophied muscle bundle in the right ventricle. The common associated lesions are ventricular septal defect followed by sub-aortic membrane. We report a child who had coarctation of aorta in association with double chambered right ventricle. This case is being reported for its rarity and challenges in management.
Double chambered left ventricle is a rare anomaly and unlike double chambered right ventricle, is not well documented. We report a case occurring with tetralogy of Fallot, an association not thus far described.
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