ORPHA:2382
Lennox-Gastaut syndrome
- Body system
- Neurological diseases
- Inheritance pattern
- Autosomal dominant, Multigenic/multifactorial, Not applicable
- Typical age of onset
- Childhood, Infancy
- Estimated prevalence
- 1-9 / 1 000 000 (Europe)
- Rarity class
- 1-9 / 1 000 000
ORPHA:2382 is classified under "Neurological diseases" in the Orphanet nomenclature.
Common signs
- Intellectual disability
- Encephalopathy
- EEG with focal sharp slow waves
- Atypical behavior
- Aggressive behavior
- Autistic behavior