Hirschsprung Disease
Hirschsprung Disease (HD) is a rare congenital disorder that occurs when nerve cells are missing from part of the intestine. It prevents normal movement of matter through the intestine, resulting in severe constipation, abdominal pain, and in some cases, small intestine blockage. HD can be life threatening if not treated in a timely manner. HD can be treated through surgical removal of the diseased part of the gut, and is often followed by the use of medications to minimize symptoms. It is important that HD is diagnosed and treated early to prevent potential complications such as bowel obstruction and gangrene. HD is a severe disorder that can have lifelong effects, and can have serious implications for the health, wellbeing and quality of life of those affected.
← Journal of Digestive Disorders And Diagnosis