Esophageal atresia
ORPHA:1199· ICD-10 Q39.1
Definition
A rare congenital malformation characterized by an interruption in the continuity of the esophagus, with or without persistent communication with the trachea. The clinical presentation varies according to the anatomy, and can lead to the inability to swallow or, in the most severe cases, respiratory distress.
- Prevalence
- 1-5 / 10 000
- Inheritance
- Not applicable
- Age of onset
- Neonatal