Abstract
Tricuspid atresia and aortopulmonary window are rare congenital cardiac anomalies. The occurrence of both these anomalies in the same patient is extremely rare, with only 1 case reported in the literature. We report the surgical management of one such patient and discuss the management issues with respect to Stage 1 single ventricle palliation.
Original language | English (US) |
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Pages (from-to) | 441-443 |
Number of pages | 3 |
Journal | Interactive cardiovascular and thoracic surgery |
Volume | 17 |
Issue number | 2 |
DOIs | |
State | Published - Aug 2013 |
Externally published | Yes |
Keywords
- Congenital heart disease
- Single ventricle
- Tricuspid atresia
ASJC Scopus subject areas
- Surgery
- Pulmonary and Respiratory Medicine
- Cardiology and Cardiovascular Medicine