EPILEPSY syndromes in children

 

Infancy / Preschool age

 – Benign myoclonic epilepsy of Infancy

 – Ohtahara syndrome (Early Infantile Epileptic Encephalopathy)

 – Infantile spasms (West syndrome)

 – Dravet syndrome

 – Doose syndrome (myoclonic–astatic seizures)

 – Lennox–Gastaut syndrome (LGS) 

 – Febrile Seizures plus (GEFS+)

 

School age

 – Childhood absence epilepsy (CAE)

 – Jeavons (Absences with Eyelid Myoclonia)

 – Rolandic (Childhood epilepsy with central-midtemporal spikes)

 – Panayiotopoulos (Childhood epilepsy with occipital paroxysms)

 – Landau–Kleffner syndrome (LKS)

 

Adolescent

 – Juvenile absence epilepsy (JAE)

 – Juvenile Myoclonic Epilepsy (JME)