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Favorable outcome of epileptic blindness in children
1Child Neurology Unit and Epilepsy Service, Meyer Children's Hospital, Rambam Medical Center, Rappaport School of Medicine, Haifa 31096, Israel. e_shahar@rambam.health.gov.il
Insights
Acute blindness in children, a rare epileptic seizure symptom, often resolves with prompt diagnosis and treatment. Early electroencephalogram (EEG) testing is crucial for timely intervention and favorable outcomes.
Area of Science:
- Neurology
- Pediatrics
- Epileptology
Background:
- Acute blindness is an uncommon manifestation of epileptic seizures.
- It involves temporary vision loss without consciousness impairment, linked to epileptic discharges on electroencephalogram (EEG).
Purpose of the Study:
- To describe epileptic blindness in children.
- To analyze seizure types, EEG findings, and treatment responses.
- To evaluate outcomes regarding vision and seizure control.
Main Methods:
- Retrospective case series of 14 children with documented epileptic blindness.
- Description of seizure characteristics, EEG findings, and therapeutic interventions.
- Assessment of visual recovery and seizure control post-treatment.
Main Results:
- All 14 children experienced temporary complete visual obscuration.
- Valproic acid and carbamazepine were effective treatments.
- Complete vision restoration occurred in all patients.
- Seizure control was achieved in most patients.
Conclusions:
- Epileptic blindness in children has a favorable prognosis with prompt diagnosis and treatment.
- Early EEG is recommended for children with acute visual obscuration.
- Appropriate therapy leads to vision recovery and seizure management.
Abstract:
Acute blindness is a rare presentation of epileptic seizures, referring to loss of sight without loss of consciousness associated with electroencephalographic (EEG) epileptic discharges, mainly representing an ictal phase but also either pre- or postictal. We report a series of 14 children with documented epileptic blindness, describing the accompanying fits and thereafter the response to therapy to resolve the blindness and control associated seizures. All patients experienced episodes of acute complete visual obscuration lasting for 1 to 10 minutes. Seven patients hadaccompanying generalized seizures, with a photosensitive response recorded in three of them. All of these seven children were treated with valproic acid, regaining full vision, and six of them became seizure free. Three patients with acute blindness who had accompanying focal motor seizures and unilateral temporooccipital posterior epileptic discharges were treated with carbamazepine regained full vision and complete seizure control. Four additional children had the constellation of migrainous headaches, focal motor phenomena, and complete blindness, along with occipital discharges compatible with Gastaut syndrome, benign childhood epilepsy with occipital paroxysms. All four patients were started on carbamazepine and became asymptomatic. Our overall experience suggests that epileptic blindness in children is associated with a favorable outcome when promptly diagnosed and treated appropriately, resulting in complete resolution of blindness in all children and satisfactory control of seizures in most of them. We therefore recommend performing a prompt EEG in any child presenting with acute visual obscuration, even in the absence of other epileptic phenomena.
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