2 or more unprovoked seizures occurring in a time frame of >24 hrs
Epilepsy
Limited to 1 part of cerebral hemisphere
Focal seizure
Involvement of all or both hemispheres
Generalized seizure
Previously
Cryptogenic epilepsy
Unknown epilepsy
Benign childhood epilepsy
With centrotemporal spikes
Age onset
3-13 yo / adolescence
Early infantile encephalopathy
Aka
Ohtahara syndrome
Severe myoclonic epilepsy of infancy
Aka as
Dravet syndrome
West syndrome
Age
2-12 mos
Lennox-gestaut syndrome
Age
2-10 yo
Caused by brain malformation
Syntaxin binding chon 1 mutations
EIEE
ohtahara syndrome
Hypsarrythmia
west syndrome