JLE

Epileptic Disorders

MENU

Perioral myoclonia with absences and myoclonic status aggravated by oxcarbazepine Volume 13, issue 3, Septembre 2011

Videos

  • Perioral myoclonia with absences and myoclonic status aggravated by oxcarbazepine
  • Perioral myoclonia with absences and myoclonic status aggravated by oxcarbazepine
  • Perioral myoclonia with absences and myoclonic status aggravated by oxcarbazepine

Figures

See all figures

Authors
Centre Neurologique William Lennox, Reference Centre for Refractory Epilepsy, Université Catholique de Louvain, Ottignies, Centre Hospitalier Régional, service de pédiatrie, Mons, Belgium

Perioral myoclonia with absences belongs to the “idiopathic generalised epilepsy syndromes in development”, currently not yet cited in the ILAE classification. This epilepsy syndrome is associated with a seizure type that appears to be specific. Here, we report polygraphic recordings of this seizure type in a young boy, previously misdiagnosed with focal epilepsy. EEG and clinical features were useful to differentiate diagnosis of his seizures from other absence or myoclonic seizures. Interestingly, some seizures were associated with neck myoclonia. Home video recording of myoclonic status aggravated by inappropriate treatment is also presented. [Published with video sequences]