T. K. Susheel Kumar, MDCor triatriatum dexter is a rare congenital cardiac anomaly with varied presentations. A high index of suspicion is necessary for accurate diagnosis and treatment.See Article page 254.Cor triatriatum dexter is a rare congenital cardiac anomaly caused by the abnormal persistence of embryonic tissue guarding the primitive sinoatrial orifice., The pathophysiology is determined by a number of factors that come into interplay, including the size of the sinoatrial orifice, the presence of atrial communication, and the degree of tricuspid valve obstruction. The manifestations are indeed variable, with clinical presentation ranging from abdominal distension and cyanosis to incidental findings during correction of other cardiac malformations., The chronicity of this lesion only adds to its protean character as illustrated in this case report.Tricuspid regurgitation is an unusual manifestation of cor triatriatum dexter and probably related to repetitive trauma and consequent deformation of the tricuspid valve leaflets from the bulging membrane. Although the authors have done a commendable job of collating the various case reports on this rare congenital heart defect from literature, the disease is under-reported and not as exotic as this study suggests. Most cases are asymptomatic and others coexist as part of other complex congenital heart defects. The study also raises an important question regarding the risks of conservative management in a largely asymptomatic child with well-documented membrane in the right atrium. The risks to the tricuspid valve tissue should not be ignored and the surgical correction of the defect can become complicated.The challenge in management of this rare disorder is primarily related to its diagnosis, as the correction itself is usually straightforward. In addition to maintaining a high index of suspicion, the usage of a second modality of imaging such as cardiac magnetic resonance imaging can go a long way in making an accurate diagnosis.