Congenitally Corrected Transposition of the Great Arteries: A Unique Case from Iraq
A severely cyanotic 27-month-old Iraqi child was transferred to the United States for surgical treatment of suspected tetralogy of Fallot. Her diagnostic studies showed dextrocardia, congenitally corrected transposition of the great arteries, hypoplastic left-sided ventricle, interrupted inferior ve...
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Published in | Pediatric cardiology Vol. 31; no. 1; pp. 120 - 123 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
New York
Springer-Verlag
2010
Springer |
Subjects | |
Online Access | Get full text |
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Summary: | A severely cyanotic 27-month-old Iraqi child was transferred to the United States for surgical treatment of suspected tetralogy of Fallot. Her diagnostic studies showed dextrocardia, congenitally corrected transposition of the great arteries, hypoplastic left-sided ventricle, interrupted inferior vena cava, and severe pulmonic stenosis. Given the anatomic constraints as well as the absence of long-term medical care, the decision was made to pursue single-ventricle palliation. The patient recovered from a superior cavopulmonary anastomosis without event and has since returned to her native Iraq. |
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Bibliography: | ObjectType-Case Study-2 SourceType-Scholarly Journals-1 ObjectType-Feature-4 content type line 23 ObjectType-Report-1 ObjectType-Article-3 |
ISSN: | 0172-0643 1432-1971 |
DOI: | 10.1007/s00246-009-9545-8 |