Which factor is NOT considered a risk for Juvenile Myoclonic Epilepsy (JME)?

Juvenile Myoclonic Epilepsy (JME) is a specific type of epilepsy that typically begins in adolescence. The risk factors associated with JME include the presence of myoclonic jerks, generalized tonic-clonic seizures, and often absence seizures as well. It is also recognized that sleep deprivation can trigger seizures in individuals with JME, emphasizing the role of lifestyle factors in managing the condition.

The age range of 14 to 15 is considered a peak onset period for JME, as the condition commonly manifests during adolescence. In contrast, the age range of 3 to 4 is not typically associated with JME. This age is more representative of childhood seizure disorders, where absence seizures or benign childhood epilepsy with centrotemporal spikes, for example, might be seen, but not JME specifically. Therefore, it is accurate to identify that being in the age group of 3 to 4 years does not represent a risk factor for JME.