Esophageal atresia (EA) and tracheoesophageal fistula (TEF) are rare conditions that develop before birth. They often occur together and affect the development of the esophagus (food pipe), trachea (windpipe) or both. These conditions can be life-threatening and must be …

What Are Tracheoesophageal Fistula and Esophageal Atresia? TEF is an abnormal opening in one or more places between the esophagus (tube going from the mouth to the stomach) and the trachea (windpipe that goes from the throat to the lungs). These are normally two separate tubes.

A tracheoesophageal fistula (TEF) is an abnormal connection between your esophagus and trachea. The condition is often congenital, which means it happened during fetal development. TEF may also be acquired in adulthood due to cancer, infection or trauma.

Tracheoesophageal Fistula (TEF) and Esophageal Atresia (EA) happen while a baby is growing during pregnancy. Most often, TEF and EA happen together. But sometimes a child has 1 condition and not the other. Each name refers to a specific problem. Doctors are not sure what causes these rare problems. They are present when a child is born ...

Esophageal atresia/tracheoesophageal fistula (EA/TEF) is a condition resulting from abnormal development before birth of the tube that carries food from the mouth to the stomach (the esophagus ). Explore symptoms, inheritance, genetics of this condition.

TEF/EA is one of the most common gastrointestinal birth defects. It has a slightly higher incidence in males than females. The incidence rate of TEF/EA is approximately 1 in 4,000 live births. Of the babies born with TEF/EA, approximately 50 percent will have an associated birth defect.

EA/TEF stands for esophageal atresia (EA) with or without tracheoesophageal fistula (TEF). While EA/TEF is rare, occurring in 1 in 2,500 births, the two conditions are often present together and develop before birth.

Esophageal atresia/tracheoesophageal fistula (EA/TEF) is a rare birth defect occurring in 1 in 2,500-4,000 babies where the esophagus fails to properly connect the mouth to the stomach. Babies with this condition must undergo surgical repair, usually shortly after birth.

Tracheoesophageal fistulas (TEFs) and esophageal atresia (EA) represent one of the most common congenital anomalies of the respiratory tract, with an incidence in approximately 1 in 3500 births. Embryology: The trachea and esophagus develop from a common primitive foregut.

EA/TEF stands for Esophageal Atresia/Tracheo-Esophageal Fistula (outside of the US, it is called OA/TOF--Oesophageal Atresia/Tracheo-Oesophageal Fistula). The exact numbers are not known, but it is a rare congenital birth defect which affects approximately 1 in …