Cor triatriatum sinister: a case series

Articles > Article · 2015

Authors: Onur IŞIK, Muhammet Akyuz, MEHMET FATİH AYIK, Erturk Levent, Yüksel ATAY

TURK KARDIYOLOJI DERNEGI ARSIVI-ARCHIVES OF THE TURKISH SOCIETY OF CARDIOLOGY, Journal Indexed in SCI Expanded, International, 2015, vol 44, pp 20-23

DOI: 10.5543/tkda.2015.04780

Summary

Objective: As a highly rare congenital defect, cor triatriatum sinister represents only 0.1% of congenital cardiac anomalies. Depending on the degree of obstruction and the accompanying symptoms, cor triatriatum can be diagnosed at any age. This case series described 5 patients with cor triatriatum sinister who underwent operation.

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