Хвороба Гіршпрунга
ORPHA:388· ICD-10 Q43.1· Hirschsprung disease
Визначення(English summary)
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.
- Поширеність
- 1-5 / 10 000
- Успадкування
- Autosomal dominant, Autosomal recessive, Multigenic/multifactorial, Not applicable
- Вік початку
- Childhood, Infancy, Neonatal