LB16.1Ангилал

Hirschsprung disease

Тодорхойлолт

This is a developmental anomaly affecting the intestinal tract characterised by congenital absence of myenteric ganglion cells (aganglionosis) in a segment of the large bowel. Due to the absence of intrinsic innervation of the muscle layers of the affected segment, there is a loss of motor function. This results in an abnormally large or dilated colon (congenital megacolon) with intestinal occlusion or constipation. This condition becomes evident shortly after birth.

Индексийн нэр томьёо Index terms · 17

Hirschsprung diseaseAganglionic megacolonaganglionosiscongenital aganglionic megacoloncongenital megacolonaganglionosis of colonbowel aganglionosiscolon aganglionosiscolonic aganglionosisHirschsprung megacolonpelvirectal achalasiaEntire colon Hirschsprung diseaseTotal aganglionosis of colon and intestineExtensive aganglionosis Hirschsprung diseaseLong segment Hirschsprung diseaseRectosigmoid Hirschsprung diseaseShort segment Hirschsprung disease

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