Abstract
A surgically treated case of absent pulmonary valve syndrome associated with type B interrupted aortic arch is presented. The presence of a restrictive ductus arteriosus promoted the development of a collateral circulation between ascending and descending thoracic aorta, allowing the child to remain clinically stable after birth.
Original language | English (US) |
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Pages (from-to) | 244-246 |
Number of pages | 3 |
Journal | Annals of Thoracic Surgery |
Volume | 66 |
Issue number | 1 |
DOIs | |
State | Published - Jul 1998 |
ASJC Scopus subject areas
- Surgery
- Pulmonary and Respiratory Medicine
- Cardiology and Cardiovascular Medicine