Catalog
Genetic epileptic syndromes with onset in infancy
Link to WHO Definition
Genetic epileptic syndromes with onset in infancy – http://id.who.int/icd/entity/1310497511
Include a vast spectrum of phenotypes having in common a genetic background and the onset in infancy. They range from benign self-remitting to severe drug resistant syndromes. Family history of epilepsy is common in some syndromic entities and exceptional in others.
Parents
Children
- 8A61.11 Dravet syndrome
- Myoclonic epilepsy in infancy or early childhood
- Epilepsy in females with intellectual development disorder with PCDH19 mutations
- 8A61.12 Epilepsy of infancy with migrating focal seizures
- Myoclonic encephalopathy in non-progressive disorders
- 8A61.10 Benign familial infantile epilepsy
- Other genetic epileptic syndromes with onset in infancy