Pediatric Hirschsprung's Disease

Children with Hirschsprung's disease are born with missing nerve cells at the end of their bowels. Hirschsprung's disease is a rare illness in which the rectum and sometimes the colon cannot function normally, resulting in serious constipation or obstruction of the bowel.

What is Pediatric Hirschsprung's Disease?

Hirschsprung's disease occurs while a baby is still developing in the mother’s womb. In a healthy developing child, the nerve cells grow from the beginning to the end of the bowel and help the colon to relax and pass stool. With Hirschsprung's disease, the child’s nerve cells do not grow to the end of the bowel.

In most cases, the nerve cells are missing from areas in the child’s rectum and sigmoid colon (part of the colon that is closest to the rectum and anus). Once the stool reaches the area where the nerve cells are missing, the blockage forms and the child develops symptoms.

What are the different types of Pediatric Hirschsprung's Disease?

There are multiple types of Hirschsprung's disease classifications.

Long-segment Hirschsprung's disease

In long-segment Hirschsprung's disease, nerve cells are missing from most or all of the large intestine and could be missing from the last segment of the small intestine.

Short-segment Hirschsprung's disease

In short-segment Hirschsprung's disease, nerve cells are missing from the last segment of the large intestine.

Entire large and small intestine

Although rare, in some children the nerve cells are missing in the entire large and small intestine.

How is Pediatric Hirschsprung's Disease diagnosed?

In order to diagnose the disorder, a biopsy of the rectal tissue is performed.

Pediatric Hirschsprung's Disease Doctors and Providers