In hirschsprung disease, there are no ganglion cells in the wall of the affected intestine. Resultados funcionales en ninos tratados quirurgicamente con. Introduction hirschsprung s disease hd is a malformation of the large intestine characterized by the absence of ganglion cells in submucosal and myenteric plexus, which produces a functional obstruction and dilatation proximal to the affected segment 1. Chronic constipation, megacolon, hirschsprungs disease. Late diagnosis of hirschsprung s disease article pdf available in journal of coloproctology 53 may 2015 with 176 reads how we measure reads. Protocolos diagnosticos y terapeuticos en pediatria. Hirschsprungs disease was a cause of neonatal obstruction in 26 22. Costos menores descenso colonico endorectal transanal. Moreover, they must sign a model release that should be sent. Hirschsprungs disease was a cause of recurrent diarrhea in 37 32. Menor dolor, menor diseccion, no genera adherencias intraperitoneales, excelente resultado estetico. B limitada al colon descendente, sigmoides y recto. Suele presentarse como estrenimiento severo con dilatacion colica proximal al segmento aganglionico.