Abstract
We report a unique case of dilated aortic root and pulmonary artery in an infant with clinical features consistent with Beals syndrome confirmed to have fibrillin-2 mutation. This case highlights a novel finding of main pulmonary artery dilatation that has not been previously reported with Beals syndrome or fibrillin-2 mutation. In addition, the importance of serial echocardiography and consideration of medical management is discussed.
| Original language | English |
|---|---|
| Pages (from-to) | 150-152 |
| Number of pages | 3 |
| Journal | Annals of Pediatric Cardiology |
| Volume | 12 |
| Issue number | 2 |
| DOIs | |
| State | Published - May 1 2019 |
Keywords
- Beals syndrome
- dilated great arteries
- fibrillin-2 mutation
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