If the upper portion of the esophagus is short and a long gap exists between upper and lower portions, reconstructive surgery cannot be performed, and the infant must receive nutrition in some way to allow several months of growth.
When a physician suspects esophageal atresia after being presented with the typical symptoms, diagnosis usually begins with gently passing a catheter through the nose and into the esophagus.
These illnesses include pneumonia and inflammations of the liver (hepatitis), brain (encephalitis), esophagus (esophagitis), large intestine (colitis), and retina of the eye (retinitis).
Type C (86.5%): Esophageal atresia with tracheoesophageal fistula, in which the upper segment of the esophagus ends in a blind pouch (EA) and the lower segment of the esophagus is attached to the trachea (TEF).
When the stomach contents moves into the esophagus, there is the possibility that this material will be aspirated into the windpipe, which can cause asthma, pneumonia, and possibly suffocation or sudden death.