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Lennox-Gastaut syndrome
Lennox–Gastaut syndrome (LGS) is a difficult-to-treat form of childhood-onset epilepsy that most often appears between the second and sixth year of life. LGS is characterized by a triad of signs including frequent seizures of multiple types, an abnormal EEG pattern of less than 2.5 Hz slow spike wave activity,[1]
LGS children with a history of perinatal hypoxia or other perinatal event have earlier age of onset of seizures[2]
Links
Endoscopic epilepsy surgery: Emergence of a new procedure
Rufinamide
Clobazam
Disease classification WHO
G40.7 Lennox-Gastaut syndrome
