Hirschsprung's disease causes: Difference between revisions
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==Causes== | ==Causes== | ||
*Normally, | *Normally, myenteric and submucosal nerve plexuses regulate motility by allowing relaxation. In the absence of their migration, there’s over contracting which prevents passage of stool. | ||
*Absence of | *Absence of myenteric and submucosal plexuses causes over contraction of the smooth muscles of the rectum causing functional obstruction and chronic constipation. | ||
*Absence of these cells in the distal colon is believed to be due to genetic mutation causing failure of migration of these cells craniocaudally. | *Absence of these cells in the distal colon is believed to be due to a genetic mutation causing failure of migration of these cells craniocaudally. | ||
*Defective differentiation of neuroblasts into neural crest cells is another suggested hypothesis explaining the disease. | *Defective differentiation of neuroblasts into neural crest cells is another suggested hypothesis explaining the disease. | ||
Revision as of 21:32, 13 June 2017
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1];Associate Editor(s)-in-Chief: Ahmed Younes M.B.B.CH [2]
Overview
Causes
- Normally, myenteric and submucosal nerve plexuses regulate motility by allowing relaxation. In the absence of their migration, there’s over contracting which prevents passage of stool.
- Absence of myenteric and submucosal plexuses causes over contraction of the smooth muscles of the rectum causing functional obstruction and chronic constipation.
- Absence of these cells in the distal colon is believed to be due to a genetic mutation causing failure of migration of these cells craniocaudally.
- Defective differentiation of neuroblasts into neural crest cells is another suggested hypothesis explaining the disease.