ABSTRACT Introduction Lennox-Gastaut syndrome (LGS) is a severe childhood-onset
epileptic encephalopathy, characterized by multiple seizure types, generalized slow spike …

Lennox‐Gastaut syndrome (LGS) is an intractable childhood‐onset epileptic
encephalopathy. Seizure freedom is rare in LGS. One of the hallmarks of LGS is medical …

Abstract Lennox-Gastaut syndrome (LGS), a childhood-onset severe developmental and
epileptic encephalopathy (DEE), is an entity that encompasses a heterogenous group of …

Lennox-Gastaut syndrome (LGS) is a severe pediatric epilepsy syndrome characterized by
mixed seizures, cognitive decline, and generalized slow (< 3Hz) spike wave discharges on …

There are currently five compounds (clobazam, felbamate, lamotrigine, topiramate,
rufinamide) available for prescription with a demonstrated efficacy on drop seizures for …

Aim To compare and rank the efficacy and safety of antiseizure medication (ASM) in patients
with Lennox–Gastaut syndrome (LGS). Method We included randomized controlled trials …

Lennox-Gastaut syndrome is an epileptic encephalopathy starting in early childhood
consisting of the triad of cognitive impairment, multiple seizures types and slow spike-wave …

Lennox-Gastaut syndrome (LGS) is one of the intractable epilepsies of childhood that is
associated with an epileptic encephalopathy. Although LGS has been accepted as a distinct …

Lennox-Gastaut syndrome (LGS) is a severe epileptic encephalopathy with a prevalence of
1–2% of all patients with epilepsy. It is characterized by multiple pharmaco-resistant seizure …

Lennox–Gastaut syndrome (LGS) is a severe epileptic and developmental encephalopathy
that is associated with a high rate of morbidity and mortality. It is characterized by multiple …