Hirschsprung disease is a large colon (intestine) disorder that causes difficulty passing feces. As a result of absent nerve cells in the baby’s intestinal muscles, the disease is inborn (congenital). The intestine contents can pile up and produce obstructions if these nerve cells do not stimulate the gut muscles to assist the contents through the gut.
Moreover, Hirschsprung disease is characterized by the inability of a newborn to have a digestive movement in the days following delivery. The disease may not be identified until later in childhood in minor cases. This condition is uncommonly diagnosed in adults. The treatment is surgery to circumvent or eliminate the affected portion of the colon.