Inoue Manabu, Kojima Yasuhiro, Kinboshi Masato, Kanda Masutaro, Shibasaki Hiroshi
Department of Neurology, Ijinkai Takeda General Hospital.
Rinsho Shinkeigaku. 2012;52(8):557-60. doi: 10.5692/clinicalneurol.52.557.
Reticular reflex myoclonus is a rare condition with only a few cases clearly documented on video. The purpose of this paper is to report a patient manifesting typical clinical picture documented on video and characteristic electrophysiological features of reticular reflex myoclonus.
A 60-year-old woman presented with spontaneous and stimulus-sensitive myoclonic jerks involving the face, neck and upper extremities following anoxic episode. The patient was investigated electrophysiologically. Surface electromyogram showed brief myoclonic activity starting from the sternocleidomastoid and spreading up to the orbicularis oculi as well as down to the upper limb muscles. Cortical somatosensory evoked potentials and long-latency reflex were not enhanced.
Clinical features and electrophysiological findings of this case are consistent with those of reticular reflex myoclonus originally reported by Hallett et al. in 1977.