Nocturnal variant of benign myoclonic epilepsy of infancy: a case series
Aparna M Prabhu1, Sheel Pathak2, Divya Khurana3
1Department of Neurosciences, Einstein Medical Center.
Insights
This study describes five children experiencing excessive myoclonic jerks exclusively during sleep, with abnormal electroencephalograms (EEGs). Researchers suggest these cases may represent a variant of benign myoclonic epilepsy of infancy.
Area of Science:
- Neurology
- Pediatric Neurology
- Clinical Neurophysiology
Background:
- Myoclonus involves brief, involuntary muscle jerks originating from the central nervous system.
- It can be physiological or indicative of underlying neurological conditions.
- Distinguishing between different types of myoclonus is crucial for diagnosis and management.
Purpose of the Study:
- To report and characterize a series of five children presenting with unique sleep-related myoclonic jerks.
- To investigate the electroencephalogram (EEG) findings during these events.
- To explore the potential classification of these findings within known epilepsy syndromes.
Main Methods:
- Case series reporting clinical observations of five children.
- Simultaneous video and electroencephalogram (EEG) monitoring during sleep.
- Analysis of EEG patterns, focusing on epileptiform discharges during myoclonic events.
Main Results:
- All five children exhibited excessive myoclonic jerks exclusively during sleep.
- Abnormal EEG activity was recorded during the myoclonic events in all cases.
- Only one-third of the events showed a clear epileptiform correlate on EEG.
Conclusions:
- The observed pattern of sleep-exclusive myoclonus with intermittent epileptiform discharges may represent a distinct clinical entity.
- Findings suggest a potential variant of benign myoclonic epilepsy of infancy.
- Further research is warranted to confirm the classification and long-term prognosis of this condition.
Abstract:
Myoclonus is a brief, rapid, involuntary muscle jerk originating in the central nervous system that can be physiological or a symptom of disease. We report a group of five children with excessive myoclonic jerks, only during sleep, and abnormal EEG during the events. Although only one third of the events had EEG epileptiform correlate, the presence of myoclonus without epileptiform EEG correlate has been described in patients with benign myoclonic epilepsy of infancy. We hypothesize that these findings may represent a variant of benign myoclonic epilepsy of infancy.
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