A 75-year-old Japanese man who had a past history of
epilepsy was admitted because of rhythmical
myoclonus of upper and lower extremities. His mother and son also had both
epilepsy and
myoclonus. On neurological examination, he was alert and oriented without
dementia. There was no abnormal finding except for the
myoclonic jerks appearing in his upper and lower extremities. The
myoclonic jerks appeared at rest and worsened during maintaining posture. Results of laboratory tests were all within normal levels. Brain MRIs were normal, and his EEGs showed diffuse fast wave activities without paroxysmal discharges. Surface EMG studies revealed irregular myoclonic discharges at the frequency of 6-20 Hz. Electrophysiologically, he had a giant somatosensory-evoked potentials, an enhanced long-loop reflex(C-reflex) and cortical spikes preceding the
myoclonic jerks, suggesting that his
myoclonus was of cortical origin. Based on the cortical
myoclonus, episodes of
epilepsy and familiarity, he was diagnosed as having familial essential
myoclonus and
epilepsy(FEME). In addition, he periodically became a motionless state characterized by sudden appearance of transient akinesia with generalized stiffness of all of his limbs. The transient motionless state usually appeared following mental stress or sudden sensory stimuli such as loud sound. It persisted for about 10-20 min and ceased spontaneously. Since EEGs recorded during this akinetorigid state showed no paroxysmal discharges, it was considered not to be epileptic. However, after the administration of
valproate, his cortical
myoclonus improved, and the transient akinetorigid state also disappeared simultaneously. From symptomatic point of views, this generalized motionless state with stiffness of limbs may resemble to freeze behavior of wild animals suddenly confronted with sudden strong stimuli. From symptomatological as well as genetic aspects, FEME has been suggested to be heterogeneous. We propose that this unique akinetorigid attack might be a new clinical phenotype of FEME.