Related Experiment Video
Updated: Aug 29, 2026

Electromagnetic Source Imaging in Presurgical Evaluation of Children with Drug-Resistant Epilepsy
Published on: September 20, 2024
Behavioral aspects of pediatric epilepsy syndromes
1Twinwoods Health Resource Centre, Milton Road, Bedford MK41 6AT, UK. FBesag@aol.com
Insights
Epilepsy syndromes in children are linked to various behavioral issues, including autism, hyperactivity, and aggression. Early treatment may improve cognitive and behavioral outcomes, but more research is needed to confirm these findings.
Area of Science:
- Pediatric Neurology
- Developmental Neuroscience
Background:
- Cognition and behavior are crucial for a child with epilepsy's independence.
- Epilepsy syndrome diagnosis informs seizure control and intellectual outcomes.
- Limited research exists on the behavioral aspects of various epilepsy syndromes.
Purpose of the Study:
- To review and synthesize the current understanding of behavioral issues associated with specific childhood epilepsy syndromes.
- To highlight the potential impact of early treatment on cognitive and behavioral outcomes.
- To identify gaps in research regarding behavioral disturbances in pediatric epilepsy.
Main Methods:
- Literature review of published studies on behavioral aspects of childhood epilepsy syndromes.
- Synthesis of reported behavioral characteristics in West syndrome, Dravet syndrome, Lennox-Gastaut syndrome, Landau-Kleffner syndrome, benign partial seizures with centrotemporal spikes, and juvenile myoclonic epilepsy.
- Discussion of the association between specific epilepsy syndromes and behavioral comorbidities like autism, hyperactivity, and aggression.
Main Results:
- West syndrome: Emerging evidence suggests early treatment may improve cognition and behavior; association between temporal lobe tubers and autism noted.
- Dravet syndrome: Associated with hyperactivity and autistic features; often treatment-resistant.
- Lennox-Gastaut syndrome: Behavioral problems include autistic features and sluggishness, likely due to ongoing seizures.
- Landau-Kleffner syndrome: Autistic features, aggression, and hyperkinesis described; behavior may improve with treatment.
- Benign partial seizures with centrotemporal spikes: Behavioral issues like concentration difficulties, hyperactivity, and impulsivity can occur.
- Juvenile myoclonic epilepsy: Linked to variable behavioral traits, potentially indicating frontal lobe dysfunction.
Conclusions:
- Specific epilepsy syndromes are associated with distinct behavioral profiles, including autistic features, hyperactivity, and aggression.
- Early and effective treatment of epilepsy, particularly in syndromes like West syndrome, shows promise for improving cognitive and behavioral outcomes.
- Further prospective studies using validated measures are essential to establish firm conclusions and understand the impact of successful epilepsy treatment on behavior.
Abstract:
Apart from control of the seizures, two of the most important factors in determining how well a child with epilepsy progresses toward independence are cognition and behavior. The diagnosis of the correct epilepsy syndrome often provides information with regard to probability of good seizure control and intellectual outcome. However, relatively little has been published on the behavioral aspects of the various epilepsy syndromes. In West syndrome there is emerging evidence that early effective treatment might improve outcome in terms of both cognition and behavior. The work on this syndrome in children with tuberous sclerosis has demonstrated an association between temporal lobe tubers and autism. In Dravet syndrome, a variety of psychiatric disorders have been reported, including hyperactivity and autistic features. This is another epilepsy syndrome that tends to be resistant to treatment, implying that the prognosis has to be guarded. The behavioral problems reported with Lennox-Gastaut syndrome also include autistic features, as well as generally sluggish behavior. It is very likely that these characteristics largely reflect the effect of ongoing seizure activity. Autistic features, aggression, and hyperkinesis have been described with Landau-Kleffner syndrome. The behavior may improve dramatically with appropriate medical treatment or after multiple subpial transection. Although the syndrome of benign partial seizures with centrotemporal or rolandic spikes is said to have a very good prognosis, it is becoming increasingly evident that behavioral problems such as concentration difficulties, tempers, hyperactivity, and impulsivity might occur. Juvenile myoclonic epilepsy has been associated with very variable behavioral traits, sometimes with immature personality features and poor social adjustment suggesting frontal lobe dysfunction. Because many of the reports of behavioral disturbance associated with epilepsy syndromes are anecdotal and do not include validated measures of behavior it would be unwise to draw firm conclusions from them at this stage. Carefully conducted prospective studies, paying particular attention to any behavioral improvements that occur with successful treatment of the epilepsy, are required.
More Related Videos
07:35Behavioral Characterization of Pentylenetetrazole-induced Seizures: Moving Beyond the Racine Scale
Published on: July 8, 2025
10:22Interictal High Frequency Oscillations Detected with Simultaneous Magnetoencephalography and Electroencephalography as Biomarker of Pediatric Epilepsy
Published on: December 6, 2016
Related Concept Videos
Epilepsy ll: Types
Epilepsy and Seizures: Overview
Various factors can trigger epilepsy, including genetic factors, brain damage, metabolic causes, and unknown etiology. Diagnosis of epilepsy involves electroencephalography (EEG), which...
Seizures: Classification
Seizures are typically classified into two main categories: focal and generalized seizures.
Focal Seizures
Focal seizures originate from specific regions of the brain. These seizures are further sub-classified into two types:
Seizures l: Introduction
Seizures ll: Types
Antiepileptic Drugs: Modulators of Neurotransmitter Release Mediated by SV2A Protein
SV2A is a transmembrane glycoprotein located predominantly in the brain, modulating the release of neurotransmitters for neuronal communication. Both levetiracetam and brivaracetam exhibit a high affinity for...