Description of the disease * EnglishPolish Pobierz sekcję do PDF Definicja 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. Disease data Klasyfikacja Morphological anomaly Synonimy CEA Congenital esophageal atresia EA/TEF Esophageal atresia with or without trachea-esophageal fistula Oesophageal atresia Kod ORPHA 1199 Kod OMIM 189960 Kod ICD10 Q39.1 Kod ICD11 LB12.1 *Soruce Extended description of the disease Pobierz sekcję do PDF No additional description. Orphanet - interntowa baza danych dotyczących rzadkich chorób i sierochych leków. ©INSERM 1999 - Dostępna na stronie www.orphanet.pl