http://www.semanticweb.org/rjyy/ontologies/2015/5/ESSO#Severe_Myoclonic_Epilepsy_in_Infancy

Severe_Myoclonic_Epilepsy_in_Infancy

ILAE 1989 Severe myoclonic epilepsy in infancy Severe myoclonic epilepsy in infancy is a recently defined syndrome. The characteristics include a family history of epilepsy or febrile convulsions, normal development before onset, seizures beginning during the first year of life in the form of generalized or unilateral febrile clonic seizures, secondary appearance of myoclonic jerks, and often partial seizures. EEGs show generalized spike-waves and polyspike-waves, early photosensitivity, and focal abnormalities. Psychomotor development is retarded from the second year of life on, and ataxia, pyramidal signs, and interictal myoclonus appear. This type of epilepsy is very resistant to all forms of treatment.

http://www.semanticweb.org/rjyy/ontologies/2015/5/ESSO#ILAE_2010_1.2_Infancy

http://www.semanticweb.org/rjyy/ontologies/2015/5/ESSO#ILAE_1989_3.1_Epilepsies_and_Syndromes_with_Both_Generalized_and_Focal_Seizures

http://www.semanticweb.org/rjyy/ontologies/2015/5/ESSO#Epilepsy_Syndrome_List_Cited_from_1989_to_2014

http://www.semanticweb.org/rjyy/ontologies/2015/5/ESSO#Engel_2001_Dravet’s_Syndrome

http://www.semanticweb.org/rjyy/ontologies/2015/5/ESSO#Epileptic_Encephalopathy