Abstract
Two neonates were taken shortly after birth to our unit with a prenatal diagnosis of [S,D,S] Tetralogy of Fallot with pulmonary atresia and “unusual” aorta to pulmonary connection. The echocardiogram confirmed the main diagnosis showing: a left aortic arch with a vascular connection between the right innominate artery and the origin of the right pulmonary artery in patient A; and right aortic arch with a vascular connection between the left innominate artery and the origin of the left pulmonary artery in patient B. (www.actabiomedica.it)
| Original language | English |
|---|---|
| Pages (from-to) | 331-332 |
| Number of pages | 2 |
| Journal | Acta Biomedica |
| Volume | 90 |
| Issue number | 2 |
| DOIs | |
| Publication status | Published - 23 May 2019 |
| Externally published | Yes |
Bibliographical note
Publisher Copyright:© Mattioli 1885.
Keywords
- Aortic arch
- Congenital heart disease (CHD)
- Tetralogy of fallot