Autosomal Dominant Nocturnal Frontal Lobe Epilepsy: ADFLE from CHRNA mutation making abnl nAChR.  Usually improve slowly over times.

SCN1A-Genetic Epilepsy with Febrile Seizures Plus including Dravet syndrome, assoc with hemiplegic migraine.

KCNQ2-benign familial neonatal seizures.

Lafora progressive myoclonus, recurr seizures with decline in intellectual function. Caused by NHLRC1 and/or EPM2A gene causing abnl Malin or Laforin protein.