PURPOSE: We performed a retrospective study to investigate seizure, EEG, social and
cognitive outcome in adult LGS subjects. METHODS: We retrospectively evaluated 27 LGS�…

Lennox–Gastaut syndrome (LGS) is a severe epileptic encephalopathy with childhood onset
that usually continues through adolescence and into adulthood. In the long term, patients�…

The variable presentation and progression of Lennox–Gastaut syndrome (LGS) can make it
difficult to recognize, particularly in adults. To improve diagnosis, a retrospective chart�…

Lennox‐Gastaut syndrome (LGS) is a rare epileptic encephalopathy with a peak age of
onset of 3–5 years of age. Reported prevalence rates for LGS vary widely from 1–10% of all�…

Purpose: To determine if using more stringent criteria for cryptogenic Lennox‐Gastaut
syndrome (LGS) would result in an improved prognosis for that group. Cryptogenic�…

Lennox-Gastaut syndrome (LGS) is a rare, age-related syndrome, characterized by multiple
seizure types, a specific electro-encephalographic pattern, and mental regression. However�…

PURPOSE: Lennox–Gastaut syndrome (LGS) is an uncommon epileptic encephalopathy. In
this study, we tried to determine the clinical and EEG characteristics of patients with LGS in�…

The authors used the definition of the Lennox-Gastaut syndrome (LGS) adopted by the
Commission on Classification and Terminology of the International League against�…

Lennox‐Gastaut syndrome (LGS) is a severe, chronic, epileptic encephalopathy, primarily
with childhood onset, which is characterised by a triad of features: multiple seizure types�…

ABSTRACT Although Lennox‐Gastaut syndrome (LGS) typically begins during childhood, it
frequently persists through adolescence and on into adulthood. It may also, rarely, have late�…