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Startle-Induced Epileptic Spasms: A Clinical and Video-EEG Study
Zhao Xu1, Xianru Jiao1, Pan Gong1
1Department of Pediatrics, Peking University First Hospital, Beijing, China.
Frontiers in Neurology
|July 5, 2022
Summary
Startle-induced epileptic spasms (ES) often originate in the frontal cortex, particularly in patients with brain lesions. These seizures are frequently drug-resistant, impacting psychomotor development.
Area of Science:
- Neurology
- Epileptology
- Neurophysiology
Background:
- Epileptic spasms (ES) are a challenging epilepsy syndrome.
- Startle-induced epileptic spasms (ES) represent a specific subtype requiring detailed characterization.
Purpose of the Study:
- To delineate the clinical characteristics of startle-induced ES.
- To identify the brain regions of origin for startle-induced ES.
Main Methods:
- Analysis of 30 patients with startle-induced ES using video-electroencephalogram (EEG) and seizure semiology.
- Evaluation of clinical data, neuroimaging, interictal epileptiform discharges, and ictal high-frequency oscillations (HFOs).
Main Results:
- The mean age of onset was 28.1 months, with half having structural etiology.
- Frontal cortex abnormalities were common (60%), and anterior ictal HFOs were significantly higher than posterior ones (p < 0.05).
- Most patients experienced mild to severe psychomotor developmental delay; seizures were often drug-resistant.
Conclusions:
- Startle-induced ES are frequently associated with brain lesions and drug resistance.
- Neuroimaging and EEG findings, including ictal HFOs, suggest a frontal cortex origin for these seizures.
Keywords:
clinical characteristicelectroencephalogramepileptic spasms (ES)high-frequency oscillationsstartle seizureMore Related Videos
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