Pediatric Short Bowel Syndrome

Children with short bowel syndrome (SBS) need care from a team of pediatric specialists, including gastroenterologists (GI doctors) and dietitians. Children's Health℠ is home to the only intestinal rehabilitation program in North Texas, which brings together all the specialists your child needs. Our team provides the latest treatments and personalized care to help your child best manage their condition and get the nutrition they need to thrive.

What is Pediatric Short Bowel Syndrome?

Pediatric SBS means that a large part of a child's small intestine is missing or doesn’t work the way it should. SBS can occur in newborns or older children. Sometimes it results from a condition that is present at birth (congenital). In other cases, it can happen after doctors surgically remove a large part of the small intestine because of an infection, injury or chronic condition.

The small intestine is essential for absorbing water and nutrients from the food we eat. Children with SBS don’t have enough healthy small intestine to stay hydrated and absorb the nutrients they need to grow and thrive. This condition requires treatment and follow-up care throughout childhood.

Pediatric Short Bowel Syndrome Doctors and Providers

Our intestinal rehabilitation team includes top pediatric experts in gastroenterology, surgery, nutrition, social work and more. Together, we provide personalized care for your child and family to help manage their unique condition and enjoy the best quality of life.

Frequently Asked Questions

  • What types of surgery can lead to short bowel syndrome?

    In newborns, SBS may occur after surgery to treat necrotizing enterocolitis, congenital problems of the bowel, or meconium ileus, a type of bowel obstruction. In older children, short bowel syndrome may occur after surgery to treat Crohn’s disease, cancer, bowel injury or a type of bowel obstruction called intussusception.

  • What is the long-term outlook for a child with short bowel syndrome?

    The outlook varies based on which parts of the small intestine are missing and how much of the small intestine is working as it should. There is no cure for SBS, but many effective treatment options are available to manage the condition.

    Children with SBS often need lifelong follow-up care. Our team is by your family’s side providing the care your child may need to help them achieve their healthiest, happiest future. When your child turns 18, we help them transition to adult specialists in SBS.