Abstract
Cervical aortic arch (CAA) and retro-aortic innominate vein (RAIV) are rare entities which can be associated with one another in a structurally normal heart. Less well recognized is the fact, that a third entity may often be present as well, since aortic arch abnormalities are common in a CAA. Hence, these three entities (CAA, RAIV, and an arch anomaly – in this case a post-ductal coarctation) may present as a triad. We present the first prenatal diagnosis of this rare triad which can be explained by common embryological origins which are discussed along with instructive aspects in diagnosis and management.
| Original language | English |
|---|---|
| Pages (from-to) | 1657-1661 |
| Number of pages | 5 |
| Journal | Echocardiography |
| Volume | 38 |
| Issue number | 9 |
| DOIs | |
| State | Published - Sep 2021 |
| Externally published | Yes |
Keywords
- aortic arch
- coarctation
- congenital heart defects
- congenital heart disease
- fetal echocardiography