Oesophageal Atresia
Information about your child
Source: NHS
In this topic (9)
If your child hadoesophageal atresia as a baby, your clinical team will pass information about him or her on to the National Congenital Anomaly and Rare Diseases Registration Service (NCARDRS).
This helps scientiststo better understand the condition. You can opt out of the register at any time.