Epilepsy syndromes

Severe myoclonic epilepsy of infancy is known as dravet syndrome. It is a type of epilepsy triggered by fever. Panayiotopoulos syndrome occurs in normal children called idiopathic epilepsy. Lennox-gastaut syndrome is a form of severe epilepsy that is characterized by multiple seizures and intellectual disability, usually between ages 3 and 5. Landau Kleffner syndrome is also childhood disorder. It is characterized by the loss of language comprehension and verbal expression in with severely abnormal electroencephalographic (EEG) findings during sleep and clinical seizures




  • Track 1-1 Panayiotopoulos syndrome
  • Track 2-2 Lennox gastaut
  • Track 3-3 Dravet syndrome
  • Track 4-4 Epilepsy imitator
  • Track 5-5 Childhood absence epilepsy
  • Track 6-6 Landau-kleffner

Related Conference of Neuroscience