Hirschsprung’s Disease | Overview

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What is Hirschsprung's disease?

Hirschsprung's (say: "hersh-sprungz") disease is a birth defect that affects the large intestine (bowel). In a normal intestine, nerve cells called ganglion (say: "gang-glee-on") cells tell muscles in the intestine to push stools through the intestine and out of the body. A child who has Hirschsprung's disease is missing these nerve cells in a part of the intestine. As a result, stools do not move properly through the intestine and severe constipation and even bacterial infection can develop. Sometimes the ganglion cells are missing from just a small part of the large intestine near the anus. Other times, the cells may be missing from a large part of the large intestine.

Source

Hirschsprung's Disease: Diagnosis and Management by J Kessmann, M.D. (American Family Physician October 15, 2006, http://www.aafp.org/afp/20061015/1319.html)

Written by familydoctor.org editorial staff

Reviewed/Updated: 03/14
Created: 12/06

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