Anal atresia is a congenital condition in which the opening of the anus is absent or obstructed. Most of the time, anal atresia can be corrected.


Anal atresia is a congenital defect, discovered at birth.

Risk Factors

A risk factor is something that increases your chance of getting a disease or condition.

The following factors increase your child's chance of developing anal atresia. If your child has either of these risk factors, tell your child's doctor:

  • Being born with other birth defects
  • Being male


If your child experience any of these symptoms do not assume it is due to anal atresia. These symptoms may be caused by other, less serious health conditions. If your child experiences any one of them, see your child's physician.

  • No anal opening present at birth
  • Anal opening in the wrong location
  • Baby does not pass the first stool within 24-48 hours after birth
  • Stool being excreted through the vagina, penis, scrotum, or urethra
  • Tight, swollen stomach
  • No bowel control by age 3


Your doctor will ask about your child's symptoms and medical history, and perform a physical exam. Tests may include the following:

  • Physical examination to determine the presence and location of the anus
  • Abdominal x-ray —type of x-ray that uses radiation to take a picture of structures inside the abdomen.
  • Enema—the injection of liquid into the intestine by way of the anus (for cleansing or examination)


Talk with your child's doctor about the best treatment plan for your child. Treatment options include the following:


This is performed to reconstruct the anus.


Temporary surgical procedure to help rid the body of waste until the condition can be corrected. In this procedure, the rectum is closed-off and a stoma (an opening) is made in the abdomen so that waste can pass through it and into a colostomy bag.

Temporary Colostomy of an Infant

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Because it is a congenital birth defect, there is no known way to prevent anal atresia.