Hirschsprung disease
What is Hirschsprung disease?
A rare congenital intestinal motility disorder that is characterized by signs of intestinal obstruction due to the presence of an aganglionic segment of variable extent in the terminal part of the colon.
Other condition names
- Aganglionic megacolon
- Congenital intestinal aganglionosis
- HSCR
Inheritance type
Autosomal dominant, Autosomal recessive, Multigenic/multifactorial, Not applicable
Age of Onset
- Childhood
- Infancy
- Neonatal
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