" /> Haddad syndrome - CISMeF





Preferred Label : Haddad syndrome;

ICD-11 definition : Haddad syndrome is a rare genetic congenital disorder in which congenital central hypoventilation syndrome (CCHS), or Ondine syndrome, occurs concurrently with Hirschsprung disease. Intestinal aganglionosis is more extensive than in classical Hirschsprung disease.;

Details


Keyword's position in hierarchy(ies) : arborescence

You can consult :

Haddad syndrome is a rare genetic congenital disorder in which congenital central hypoventilation syndrome (CCHS), or Ondine syndrome, occurs concurrently with Hirschsprung disease. Intestinal aganglionosis is more extensive than in classical Hirschsprung disease.

Nous contacter.
07/07/2025


[Home] [Top]

© Rouen University Hospital. Any partial or total use of this material must mention the source.