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Published on: September 6, 2017
Clinical profile of partial seizures beginning at less than four years of age
1Epilepsy Unit, University Hospital, London, Ontario, Canada.
Insights
Early-onset partial seizures in children often present with motor symptoms. Electroencephalography (EEG) and neuroimaging reliably localize seizure origins, aiding diagnosis.
Area of Science:
- Pediatric Neurology
- Epilepsy Research
- Clinical Neurophysiology
Background:
- Recurrent partial seizures beginning in early childhood (<= 47 months) present unique clinical challenges.
- Understanding the diverse seizure manifestations and origins is crucial for effective management.
Purpose of the Study:
- To analyze the clinical features, electroencephalographic (EEG) findings, and neuroimaging results in a cohort of pediatric patients with early-onset partial seizures.
- To determine the reliability of interictal EEG and computed tomography (CT) scans in localizing seizure onset.
Main Methods:
- Retrospective review of clinical data, EEG recordings, and CT scans from 46 patients with early-onset partial seizures.
- Correlation of seizure semiology, EEG abnormalities (spikes, delta activity), neurological signs, and CT findings with the lobe/hemisphere of seizure origin.
Main Results:
- Motor seizures were prevalent (80%), occurring unilaterally, bilaterally, or both. Complex partial seizures (CPS) were common (72%).
- EEG accurately localized seizure origin in most cases (spikes 97%, delta activity 92%). Neurological signs and CT findings also correlated well with seizure origin (90% for CT).
- Frontal lobe seizures were most frequent (48%), followed by temporal lobe (30%). Cortical developmental abnormalities were the leading cause (26%).
Conclusions:
- Early-onset partial seizures exhibit varied clinical presentations.
- Interictal EEG and neuroimaging are highly effective tools for lateralizing and localizing the seizure onset zone in pediatric epilepsy.
- Cortical developmental abnormalities are a significant etiology in this patient group.
Abstract:
Clinical features of all our 46 patients whose recurrent partial seizures began at age less than or equal to 47 months were studied. Thirty-seven (80%) had motor seizures which were exclusively unilateral in 14 patients, bilaterally synchronous in 8, and both unilateral and bilaterally synchronous in 15. Thirty-three patients (72%) had complex partial seizures (CPS), and 11 patients (24%) had simple partial somatosensory seizures. Clinical seizures were recorded by EEG in 18 patients (39%), and a subclinical (larval) seizure was recorded in 1; those in 10 patients arose from a temporal lobe, 4 were from a frontal lobe, and in 5 they involved two adjacent lobes from onset. Several extra-ictal features reliably indicated lobe or hemisphere of seizure onset. The lobe of principal interictal EEG spikes corresponded to seizure origin in 33 of 34 patients (97%), and regional delta activity corresponded to lobe of seizure origin in 22 of 24 patients (92%). The seizures of all 13 patients with unilateral neurologic signs corresponded to the hemisphere implicated by the deficit. Computed tomography (CT) scan showed lesions in 30 patients (65%) and corresponded to the lobe of seizure onset in 27 of the 30 (90%). Seizures arose primarily from a frontal lobe in 22 of 46 patients (48%), from a temporal lobe in 14 patients (30%), and from an occipital-parietal-posterotemporal region in 6 patients (13%); only the hemisphere of origin could be determined in 4 patients. Cortical developmental abnormalities were the most common known cause (12 patients, 26%); febrile seizures and primary brain tumors occurred in 10 and 8 patients, respectively.(ABSTRACT TRUNCATED AT 250 WORDS)
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