We studied myoclonic seizures (MS) in 5 patients with juvenile myoclon
ic epilepsy (JME) using video polygraphic recordings to investigate th
e clinical characteristics of MS in this epileptic syndrome. The total
number of MS analyzed was 302 (range 27-125, mean 60) seizures per pa
tient. MS occurred either singly or repetitively (37 vs. 63%) and corr
esponded to generalized bilaterally synchronous single or multispike-a
nd-wave complexes at 3-5 Hz. Video analysis of the myoclonic jerks dem
onstrated that either distal or proximal muscle involvement predominat
ed. In the former, there was mild bilateral flexion and some external
rotation of the forearms. In the latter, flexion of both arms at the e
lbow, flexion and abduction of the thighs, and extension of the back w
as observed. Asymmetry of MS was noted in 4 of 5 patients. Facial invo
lvement of MS occurred infre quently in 2 patients. When the patients
kept both arms outstretched, the arms dropped or there was sudden inte
rruption of ongoing electromyographic (EMG) potentials immediately aft
er myoclonic jerks (postmyoclonic inhibition) in all patients. One sho
uld inquire about these clinical characteristics of MS in JME when tak
ing a thorough history in patients with primary generalized tonic-clon
ic seizures (GTC).