Esophageal atresia (EA)
What is esophageal atresia (EA)?
Esophageal atresia (EA) - a rare congenital birth defect - is a malformation that obstructs the upper esophagus. The atresia causes the child to have difficulties with swallowing and eating. Many newborns with esophageal atresia also have congenital heart defects, rectal or spinal malformations and kidney problems.
What are the signs and symptoms of esophageal atresia (EA)?
Blue skin (usually when feeding)
Breathing trouble
Coughing, choking (when feeding)
Round, full abdomen
Other birth defects
What is the cause of esophageal atresia (EA)?
The direct cause is unknown but research suggests that is it genetic.
How is esophageal atresia (EA) treated?
Infants with esophageal atresia require surgery to repair the connections between the esophagus and trachea and prevent complications.
Esophageal atresia (EA) doctors and providers
- Megha Mehta, MDPediatric Gastroenterologist
- Rinarani Sanghavi, MDPediatric Gastroenterologist
- Jennifer Peacock, APRN, PNP-PCNurse Practitioner - Gastroenterology