ORPHA:33543
Kleine-Levin syndrome
- Body system
- Neurological diseases
- Inheritance pattern
- Not documented in Orphadata
- Typical age of onset
- Adolescent, Adult, Childhood
- Estimated prevalence
- 1-9 / 1 000 000 (Europe)
- Rarity class
- 1-9 / 1 000 000
ORPHA:33543 is classified under "Neurological diseases" in the Orphanet nomenclature.
Common signs
- Confusion
- Episodic hypersomnia
- Cognitive impairment
- Amplification of sexual behavior
- Photophobia
- Agitation