Childhood-onset epilepsy syndrome

Part of

Sub-types of Childhood-onset epilepsy syndrome

• Familial partial epilepsy 0 trials · 39 incl. sub-types
  7 sub-types

  • Temporal lobe epilepsy 31 trials Sub-types →
  • Mesial temporal lobe epilepsy with hippocampal sclerosis 10 trials
  • Self-limited epilepsy with centrotemporal spikes 3 trials Sub-types →
  • Generalized epilepsy-paroxysmal dyskinesia syndrome 1 trial
  • Autosomal dominant epilepsy with auditory features 0 trials
  • Familial focal epilepsy with variable foci 0 trials Sub-types →
  • Familial sleep-related hypermotor epilepsy 0 trials Sub-types →
• Childhood-onset epilepsy syndrome with developmental and/or epileptic encephalopathy 0 trials · 37 incl. sub-types
  5 sub-types

  • Lennox-Gastaut syndrome 26 trials · 27 incl. sub-types Sub-types →
  • Developmental and/or epileptic encephalopathy with spike-wave activation in sleep 8 trials Sub-types →
  • Epilepsy with myoclonic atonic seizures 1 trial
  • Febrile infection-related epilepsy syndrome 1 trial
  • Idiopathic hemiconvulsion-hemiplegia syndrome 0 trials
• New-onset refractory status epilepticus 8 trials
• Childhood-onset idiopathic generalized epilepsy syndrome 0 trials · 7 incl. sub-types
  1 sub-type

  • Childhood absence epilepsy 7 trials Sub-types →
• Childhood-onset self-limited focal epilepsy syndrome 0 trials · 3 incl. sub-types
  4 sub-types

  • Self-limited epilepsy with centrotemporal spikes 3 trials Sub-types →
  • Childhood occipital visual epilepsy 0 trials
  • Photosensitive occipital lobe epilepsy 0 trials
  • Self-limited epilepsy with autonomic seizures 0 trials
• Atypical childhood epilepsy with centrotemporal spikes 1 trial
• Rolandic epilepsy-speech dyspraxia syndrome 0 trials · 1 incl. sub-types
  2 sub-types

  • Rolandic epilepsy, intellectual disability, and speech dyspraxia, X-linked 1 trial
  • GRIN2A-related rolandic epilepsy-speech dyspraxia syndrome 0 trials
• Landau-Kleffner syndrome 0 trials
• Sunflower syndrome 0 trials
• Acute encephalopathy with biphasic seizures and late reduced diffusion 0 trials
• Childhood-onset genetic generalized epilepsy syndrome 0 trials
  2 sub-types

  • Epilepsy with eyelid myoclonia 0 trials
  • Epilepsy with myoclonic absences 0 trials
• Cryptogenic late-onset epileptic spasms 0 trials
• Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation 0 trials
• Perioral myoclonia with absences 0 trials
• Rolandic epilepsy-paroxysmal exercise-induced dystonia-writer's cramp syndrome 0 trials
• Self-limited childhood occipital epilepsy 0 trials
  2 sub-types

  • Childhood occipital visual epilepsy 0 trials
  • Self-limited epilepsy with autonomic seizures 0 trials