Esophageal atresia

MONDO:0001044

A congenital abnormality of the esophagus in which the upper esophagus ends as a blind pouch and does not connect with the lower esophagus; it is often accompanied by a tracheoesophageal fistula. Signs and symptoms in a newborn with this abnormality include excessive salivation, choking, coughing, and the development of cyanosis and respiratory distress when fed.

Also known as: congenital atresia of esophagus, congenital atresia of oesophagus, congenital esophageal atresia, congenital imperforate oesophagus, esophageal atresia, esophageal atresia (disease), imperforate oesophagus

22 clinical trials for this condition and its sub-types.

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