Juvenile myoclonic epilepsy (JME) is a heterogeneous genetic generalized epilepsy (GGE) syndrome starting around puberty, comprising 5-10% of all epilepsies in large cohorts [1]. Myoclonic jerks of upper extremities, predominantly occurring after awakening, without loss of consciousness, constitute its main feature. Other seizure types are absences and tonic-clonic seizures (TCS) [2,3] and/or myoclonic-tonic-clonic seizures (MTCS) according to the 2017 ILAE classification of seizures [4,5].

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