Hirschsprungs disease was a cause of neonatal obstruction in 26 22. Hirschsprungs disease was a cause of recurrent diarrhea in 37 32. Early recognition and surgical correction of hirschsprung disease protects affected infants from enterocolitis and debilitating constipation. Hirschsprungs disease as a rare cause of refractory.
B limitada al colon descendente, sigmoides y recto. Article pdf available january 2017 with 2,015 reads. Protocolos diagnosticos y terapeuticos en pediatria. Total colonic aganglionosis associated with interstitial deletion of the long arm of chromosome 10. Dec 30, 2019 in 1886, harold hirschsprung first described hirschsprung disease as a cause of constipation in early infancy. Late diagnosis of hirschsprung s disease article pdf available in journal of coloproctology 53 may 2015 with 176 reads how we measure reads. Costos menores descenso colonico endorectal transanal. The affected segment is of small caliber with proximal dilatation. Hirschsprung disease aganglionosis, colonic colonic aganglionosis megacolon, congenital aganglionosis, rectosigmoid colon aganglionosis, total colonic congenital megacolon. 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. Familial dysautonomia is caused by mutations of the ikap gene.
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