Hirschsprung's Disease

Usually seen at birth, Hirschsprung disease is a large intestine condition affecting the ability to pass stool through the intestines.

Surgery is the only option for treatment choices in Hirschsprung disease.

Hirschsprung's Disease is disease of the large intestine. Not a lot of people know about this disease, because it's still considered a rare disease.

The Danish doctor, Harald Hirschsprung was the first doctor to document and describe this congenital disorder of the colon in 1866. He discovered this illness when he conducted autopsies on two infants who had died due to engorged bellies.

This congenital disorder causes intestinal blockages and pain. Although it can be difficult to deal with pain in youngsters too young to talk about it, several techniques help doctors diagnose Hirschsprung's disease.

It can be terrifying for parents to watch an undiagnosed baby with Hirschsprung's disease. The youngster can't tell them where it hurts. Although this intestinal disorder is present at birth, sometimes signs don't appear until the individual is an adult.

Hisrchsprung's Disease is a disease that affects the colon and the ability of the colon to function as it should. My article gives a few details.

When to suspect that the newborn has got Hirschsprung's disease and how to diagnose? What are the procedures for treatment?

HD is a congenital or birth defect. Children are born without ganglion cells, which control the muscles of the colon that push food and digested waste through the large intestine. Treatment only available by surgery, including a pull-through procedure.

The colon can become enlarged, which it will become difficult to have a bowel movement; a condition referred to as megacolon or giant colon. Nerve damage or deficiencies in the colon or rectum is the cause of a megacolon.