ORPHA:661
Congenital central hypoventilation syndrome
Also called Ondine curse, Ondine syndrome, CCHS, Congenital central alveolar hypoventilation syndrome
- Body system
- Neurological diseases
- Inheritance pattern
- Autosomal dominant, Not applicable
- Typical age of onset
- Infancy, Neonatal
- Estimated prevalence
- 1-9 / 1 000 000 (France)
- Rarity class
- 1-9 / 1 000 000
ORPHA:661 is classified under "Neurological diseases" in the Orphanet nomenclature.
Common signs
- Respiratory insufficiency
- Abnormality of the autonomic nervous system
- Seizure
- Hypotonia
- Aganglionic megacolon
- Ganglioneuroma