Lennox-Gastaut syndrome
ORPHA:2382· ICD-10 G40.4
Definition
A rare, severe early-onset developmental epileptic encephalopathy characterized by the triad of intellectual impairment, multiple seizure types, and typical electroencephalography (EEG) abnormalities.
- Prevalence
- 1-9 / 1 000 000
- Inheritance
- Autosomal dominant, Multigenic/multifactorial, Not applicable
- Age of onset
- Childhood, Infancy