Congenital megacolon, also known as Hirschsprung’s disease, is one of the main types of megacolon disorder. This causes a massive enlargement and dilation of the large intestine colon. Generally, this disorder, often diagnosed in infancy, is characterized by the lack of ganglions or the particular nerve cells in the bowel segment. The lack of ganglion causes the bowels’ muscles to lose their capability to let the stool move through the intestine.
Congenital megacolon is a severe genetic condition that requires proper care. With the right treatment, children with this condition can live a normal life. However, they may still have bowel issues on and off into adulthood since congenital megacolon is a lifelong issue that should always be observed.