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Overview
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Seizure Classification
Generalized onset seizure
Motor Onset
Tonic-clonic and variants
Tonic
Atonic
Myoclonic
Myoclonic-atonic
Epileptic spasms
Non-Motor Onset
Typical Absence
Atypical Absence
Myoclonic Absence
Absence with Eyelid Myoclonia
Focal Onset Seizure
By Onset Feature
Awareness
Aware
Impaired awareness
Motor Onset
Non-Motor Onset
Sensory
Cognitive
Autonomic
Emotional
Behaviour Arrest
Focal to Bilateral Tonic-Clonic
Hemispheric lateralization
Lobar localization
Frontal
Temporal
Parietal
Occipital
Unknown Onset Seizure
Epilepsy Classification
Generalized Epilepsy
Focal Epilepsy
Generalized and Focal Epilepsy
Unknown Epilepsy
Epilepsy Syndromes
Neonatal/Infantile
Self-limited neonatal seizures and Self-limited familial neonatal epilepsy
Self limited familial and non-familial infantile epilepsy
Early myoclonic encephalopathy
Ohtahara syndrome
West syndrome
Dravet syndrome
Myoclonic epilepsy in infancy
Epilepsy of infancy with migrating focal seizures
Myoclonic encephalopathy in non-progressive disorders
Febrile seizures plus, genetic epilepsy with febrile seizures plus
Childhood
Epilepsy with myoclonic-atonic seizures
Epilepsy with eyelid myoclonias
Lennox-Gastaut syndrome
Childhood absence epilepsy
Epilepsy with myoclonic absences
Panayiotopoulos syndrome
Childhood occipital epilepsy (Gastaut type)
Photosensitive occipital lobe epilepsy
Childhood epilepsy with centrotemporal spikes
Atypical childhood epilepsy with centrotemporal spikes
Epileptic encephalopathy with continuous spike-and-wave during sleep
Landau-Kleffner syndrome
Autosomal dominant nocturnal frontal lobe epilepsy
Adolescent/Adult
Juvenile absence epilepsy
Juvenile myoclonic epilepsy
Epilepsy with generalized tonic-clonic seizures alone
Autosomal dominant epilepsy with auditory features
Other familial temporal lobe epilepsies
Any Age
Familial focal epilepsy with variable foci
Reflex epilepsies
Progressive myoclonus epilepsies
Epilepsy Etiologies
Genetic Etiology
Chromosomal abnormalities
Gene abnormalities
Structural Etiology
Malformations of cortical development
Overview
Focal cortical dysplasia
Tuberous sclerosis
Lissencephaly
Subcortical band heterotopia
Grey matter heterotopia
Polymicrogyria
Hemimegalencephaly
Schizencephaly
Hypothalamic hamartoma
Vascular malformations
Overview
Cerebral angioma
Sturge-Weber syndrome
Arteriovenous malformation
Hippocampal sclerosis
Hypoxic-Ischemic
Overview
Stroke
Hypoxic-Ischemic injury
Traumatic brain injury
Tumors
Overview
DNET
Ganglioglioma
Porencephalic Cyst
Metabolic Etiology
Immune Etiology
Rasmussen syndrome
Antibody mediated
Infectious Etiology
Unknown Etiology
Febrile infection related epilepsy syndrome
Epilepsy imitators
CHILDHOOD OCCIPITAL EPILEPSY (GASTAUT TYPE)
Clinical Overview
Seizures
EEG
Imaging
Genetics
Differential diagnoses
Focal seizures
due to
structural brain abnormality
Celiac disease, epilepsy and cerebral calcification syndrome
(check anti-gliadin antibodies)
Migraine with visual aura