Isolated tracheo-esophageal fistula

A rare, congenital, esophageal disorder characterized by the presence of an abnormal connection between the esophagus and the trachea (typically occurring in the lower cervical or upper thoracic area and taking an oblique path upward to trachea), without concomitant esophageal atresia. Depending on the size of the lumen, presentation varies from neonatal episodes of choking and cyanosis on feeding to subtle symptoms of wheezing and recurrent respiratory infections in childhood or early adulthood.

Also known as: H-type tracheoesophageal fistula, tracheo-esophageal fistula, tracheoesophageal fistula, isolated tracheoesophageal fistula

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