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Published on: January 29, 2018
Early-onset absence epilepsy aggravated by valproic acid: a video-EEG report
Vincenzo Belcastro1, Roberto Horacio Caraballo2, Antonino Romeo3
1Neurology Unit, Department of Neuroscience, Sant'Anna Hospital, Como, Italy.
Insights
Early-onset absence epilepsy can rarely begin in infancy. Valproic acid worsened seizures in one infant, but levetiracetam provided effective seizure control and a benign outcome.
Area of Science:
- Neurology
- Pediatric Epilepsy
Background:
- Early-onset absence epilepsy, defined by absence seizures before age 4, is a diverse group of conditions.
- Seizures beginning in the first year of life are exceptionally uncommon.
Observation:
- A case study of an 11-month-old boy experiencing absence seizures.
- Seizure frequency escalated after initiating valproic acid (VPA) therapy.
- Seizures significantly improved after discontinuing VPA, with no identifiable cause like toxicity or deficiency.
Findings:
- Levetiracetam effectively controlled absence seizures in this patient.
- The patient experienced a benign course regarding both seizure control and neuropsychological development.
- The electroclinical presentation and outcome were similar to Childhood Absence Epilepsy (CAE), suggesting a continuum within Idiopathic Generalized Epilepsy (IGE).
Implications:
- This case highlights a rare presentation of early-onset absence epilepsy with paradoxical worsening on valproic acid.
- Levetiracetam appears to be a safe and effective treatment option for such cases.
- Findings support the concept of early-onset absence epilepsies being part of a broader spectrum of idiopathic generalized epilepsies.
Abstract:
Early-onset absence epilepsy refers to patients with absence seizures beginning before age 4 and comprises a heterogeneous group of epilepsies. Onset of absence seizures in the first year of life is very rare. We report a boy with absence seizures with onset at age 11 months, whose seizures increased in frequency after the introduction of valproic acid (VPA) treatment and substantially improved upon cessation of treatment. The mechanism of seizure worsening did not involve VPA toxicity, encephalopathy, Glut-1 deficiency or overdosage, and the reason for absence seizure aggravation remained unclear. The patient showed complete control of absence seizures with levetiracetam treatment and the course was benign, both in terms of seizure control and neuropsychological aspects. The similar overall electroclinical picture and outcome between children with early-onset absences and those with CAE support the view that these conditions are a continuum within the wide spectrum of IGE. [Published with video sequences].
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