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Diagnostic criteria of sleep-related hypermotor epilepsy*

Diagnostic criteria of sleep-related hypermotor epilepsy*
Diagnosis based on clinical history
  • Brief (<2 minutes) seizures with stereotyped motor pattern, abrupt onset and offset, may cluster
  • Most common motor activity is hypermotor: vigorous hyperkinetic movements, and/or asymmetric tonic or dystonic posturing, with or without impaired awareness
  • Occurrence predominantly during sleep
  • Diagnosis not excluded by intellectual impairment, neuropsychiatric features, absence of interictal and ictal EEG correlates, extrafrontal origin
Three levels of certainty
  • Witnessed (possible)
  • Clinical features provided by observer
  • Video-documented (clinical)
  • At least one stereotyped event, confirmed by observer to be typical
  • High quality audio-video including the onset and offset with clear visualization of the entire event
  • Minor motor events or paroxysmal arousals excluded
  • Video-EEG documented (confirmed)
  • At least one stereotyped event during daytime sleep recording after sleep deprivation, or during full night sleep recording using ≥19 EEG channels, ECG, oculogram, and chin EMG
  • Definitive ictal epileptic discharge or interictal epileptiform abnormality
* Previously referred to as nocturnal frontal lobe epilepsy.
EEG: electroencephalography; ECG: electrocardiography; EMG: electromyography.
Original table modified for this publication. From: Tinuper P, Bisulli F. From nocturnal frontal lobe epilepsy to sleep-related hypermotor epilepsy: A 35-year diagnostic challenge. Seizure 2017; 44:87. Table used with the permission of Elsevier Inc. All rights reserved.
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