This is an old revision of the document!
Lennox-Gastaut syndrome
This article is a stub. Please help us improve it
Lennox-Gastaut syndrome (LGS) is an epileptic encephalopathy and is defined by a triad of multiple drug-resistant seizure types, a specific EEG pattern showing bursts of slow spike-wave complexes or generalized paroxysmal fast activity, and intellectual disability. The prevalence of LGS is estimated between 1 and 2% of all patients with epilepsy.
Discussion