Hirschsprung disease (HSCR) is the most common congenital motility disorder of the intestine, characterized by the absence of ganglion cells in the myenteric and submucosal plexuses, leading to functional bowel obstruction. Short-segment Hirschsprung disease (SS-HSCR) accounts for the majority of ca...
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| Päätekijät: | , , , |
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| Aineistotyyppi: | Artikkeli |
| Linkit: | https://doaj.org/article/2a824dffb2974590b38ca86fbbb00ae6 |
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