User:Colin/Epilepsies


 * Electroclinical syndromes
 * Neonatal period
 * Benign familial neonatal epilepsy (BFNE)
 * Early myoclonic encephalopathy (EME)
 * Ohtahara syndrome
 * Infancy
 * Benign familial infantile epilepsy
 * Benign infantile epilepsy
 * Dravet syndrome
 * Epilepsy of infancy with migrating focal seizures
 * Myoclonic encephalopathy in nonprogressive disorders
 * Myoclonic epilepsy in infancy (MEI)
 * West syndrome
 * Childhood
 * Autosomal-dominant nocturnal frontal lobe epilepsy (ADNFLE)
 * Benign epilepsy with centrotemporal spikes (BECTS)
 * Childhood absence epilepsy (CAE)
 * Epilepsy with myoclonic absences
 * Epilepsy with myoclonic atonic (previously astatic) seizures
 * Epileptic encephalopathy with continuous spike-and-wave during sleep (CSWS)
 * Febrile seizures plus (FS+) (can start in infancy)
 * Landau-Kleffner syndrome (LKS)
 * Late onset childhood occipital epilepsy (Gastaut type)
 * Lennox-Gastaut syndrome
 * Panayiotopoulos syndrome
 * Adolescence – Adult
 * Autosomal dominant epilepsy with auditory features (ADEAF)
 * Epilepsy with generalized tonic–clonic seizures alone
 * Juvenile absence epilepsy (JAE)
 * Juvenile myoclonic epilepsy (JME)
 * Progressive myoclonus epilepsies (PME)
 * Other familial temporal lobe epilepsies
 * Less specific age relationship
 * Familial focal epilepsy with variable foci (childhood to adult)
 * Reflex epilepsies
 * Distinctive constellations
 * Gelastic seizures with hypothalamic hamartoma
 * Hemiconvulsion–hemiplegia–epilepsy
 * Mesial temporal lobe epilepsy with hippocampal sclerosis (MTLE with HS)
 * Rasmussen syndrome
 * Epilepsies that do not fit into any of these diagnostic categories can be distinguished first on the basis of the presence or absence of a known structural or metabolic condition (presumed cause) and then on the basis of the primary mode of seizure onset (generalized vs. focal)
 * Epilepsies attributed to and organized by structural-metabolic causes
 * Malformations of cortical development (hemimegalencephaly, heterotopias, etc.)
 * Neurocutaneous syndromes (tuberous sclerosis complex, Sturge-Weber, etc.)
 * Angioma
 * Infection
 * Perinatal insults
 * Stroke
 * Trauma
 * Tumour
 * Etc.
 * Epilepsies of unknown cause
 * Conditions with epileptic seizures that are traditionally not diagnosed as a form of epilepsy per se
 * Benign neonatal seizures (BNS)
 * Febrile seizures (FS)