Hirschsprung’s disease
Definition Hirschsprung’s disease is a rare congenital disease. It occurs with a frequency of about 1 : 3. 000 – 5. 000 affected newborns. The disease manifests itself in the gastrointestinal tract. In one part of the intestine, nerve cells and nerve cell bundles (ganglia) are missing. This is known as aganglionosis. In addition to … Hirschsprung’s disease