Overview :

The syndromic approach of epilepsies : Classifications, epidemiology, prognosis - Genetic bases of epileptic syndromes - Animal models of epileptic syndromes - EEG traits of epileptic syndromes - Neuroimaging and epileptic syndromes - Drug development in epileptic syndromes

Syndromes in infancy and early childhood : Benign neonatal and infantile seizures and epilepsy - Severe neonatal and infantile seizures and epilepsies - Infantile spasms - Febrile seizures, GEFS+ and epilepsies with seizures triggered by fever - Dravet syndrome - Idiopathic myoclonic epilepsies in infancy and early childhood

Syndromes in childhood and adolescence : Lennox-Gastaut syndrome - Idiopathic focal epilepsies in childhood - Encephalopathy with status epilepticus during slow sleep (ESES) including Landau-Kleffner syndrome - Absence epilepsies: CAE, JAE, early absences, myoclonic absences and other syndromes - Isolated focal seizures in adolescence - Juvenile myoclonic epilepsies

Other epileptic syndromes : Rasmussen’s encephalitis - Epilepsy with generalized tonic-clonic seizures only - Temporal lobe epilepsy syndromes - Frontal lobe and other extratemporal epilepsies - Photosensitivity and syndromes - Epilepsy syndromes in the elderly

Special etiologies and situations : Epilepsy in inborn errors of metabolism - Genetically determined focal epilepsies - Autoimmune epilepsies and encephalopathies - Brain parasitic infestations - Complex and other reflex epilepsies - Epilepsy and chromosomal disorders and CNV - Progressive myoclonus epilepsies - Epilepsy and cortical malformations