Congenital Abnormality
esophageal atresia
e·soph·a·ge·al a·tre·sia [ ih-sof-uh-jee-uhl, ee-suh-faj-ee-uhl uh-tree-zhuh, -zhee-uh ]
Subclass of:
Congenital digestive system anomalies;
Esophageal Diseases
Definitions related to esophageal atresia:
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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.NCI ThesaurusU.S. National Cancer Institute, 2021
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A developmental defect resulting in complete obliteration of the lumen of the esophagus such that the esophagus ends in a blind pouch rather than connecting to the stomach.Human Phenotype Ontology (HPO)The Human Phenotype Ontology Project, 2021
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Congenital abnormality characterized by the lack of full development of the ESOPHAGUS that commonly occurs with TRACHEOESOPHAGEAL FISTULA. Symptoms include excessive SALIVATION; GAGGING; CYANOSIS; and DYSPNEA.NLM Medical Subject HeadingsU.S. National Library of Medicine, 2021
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Esophageal atresia is incomplete formation of the esophagus, frequently associated with tracheoesophageal fistula. Diagnosis is suspected by failure to pass a nasogastric or orogastric tube. Treatment is surgical repair.Merck & Co., Inc., 2020
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Oesophageal atresia (OA) encompasses a group of congenital anomalies with an interruption in the continuity of the oesophagus, with or without persistent communication with the trachea.National Center for Advancing Translational Sciences
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