Catalog
Genetic epileptic syndromes with childhood onset
Link to WHO Definition
Genetic epileptic syndromes with childhood onset – http://id.who.int/icd/entity/1612372804
Parents
Children
- 8A61.20 Benign childhood epilepsy with centro-temporal spikes
- Perioral myoclonia with absences
- Rolandic epilepsy-paroxysmal exercise-induced dystonia-writer's cramp syndrome
- Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation
- Jeavons syndrome
- 8A61.23 Myoclonic absences or absences with myoclonias
- Rolandic epilepsy-speech dyspraxia syndrome
- Cryptogenic late-onset epileptic spasms
- Generalised epilepsy with febrile seizures plus
- Benign occipital epilepsy
- Myoclonic epilepsy in early childhood
- 8A61.21 Childhood absence epilepsy
- Generalised epilepsy - paroxysmal dyskinesia
- 8A61.22 Epilepsy with myoclonic-astatic seizures