To determine the survival of patients with esophageal atresia born in Bogota, in addition to the clinical results of treatment, comparing some variables with their healthy controls. Methodology: The database monitoring program Congenital Malformations of Bogota (BCMSP) was used to obtain data from patients born with esophageal atresia between January 2009 and December 2013, 22 patients were included in the study. To Inquire about the current health status of the case, determining whether they were alive or dead. Information on perinatal history, type of esophageal atresia, surgeries performed, and the presence of respiratory, gastrointestinal symptoms, and musculoskeletal after surgery and a year of life, as well as information controls that attended the pediatric surgeon was obtained . A similar questionnaire, inquiring about perinatal history was made to a group of 22 healthy controls. Results Average 3.9 months, with 1.2 children per child aged study. Over half of the patients had no prenatal diagnosis. Currently half of the patients survived. 59% of patients experienced some type of fistula. 50% had the first surgery between the first or second day of life. More than half had any complications. In evaluating persistent symptoms 20% had respiratory infections, gastroesophageal reflux and dysphagia occurred in equal proportion of patients, and the year continued with these symptoms. Between cases and controls significant difference between gestational age and birth weight being lower for cases they were found.