Hirschsprung Disease
Hirschsprung Disease is a rare congenital disorder which causes a blockage in the large intestine, resulting in an inability to pass waste through the colon. This is caused by lack of nerve cells in the wall of the intestine, preventing muscles from contracting and making it difficult for waste to move through the gut. Symptoms of Hirschsprung Disease include constipation, abdominal pain, vomiting, and distention of the abdomen. Treatment options include surgery to remove the affected segment of intestine and to create a pathway for waste to exit, or insertion of a stoma to bypass the blockage. Hirschsprung Disease is a serious disorder which can cause severe complications if not treated, and can be life-threatening. Early diagnosis and treatment are essential for successful management of the condition.
← International Journal of Neonatology