Adult myoclonic epilepsy: A distinct syndrome of idiopathic generalized epilepsy

The authors present 11 cases of idiopathic generalized epilepsy that began in adulthood at a mean age of 39 years. All patients had myoclonic jerks, f ive had absence seizures, and nine had infrequent generalized tonic-clonic seizures. A majority had a family history of seizures. EEG in all patients showed generalized epileptiform abnormalities, whereas neuroimaging and neu rologic examination results were normal. This series appears to represent a previously undescribed idiopathic generalized epilepsy syndrome of adult m yoclonic epilepsy.