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Published on: July 8, 2025
Neurobehavioral abnormalities may correlate with increased seizure burden in children with Panayiotopoulos syndrome
Yoshiko Hirano1, Hirokazu Oguni, Makoto Funatsuka
1Department of Pediatrics, Tokyo Women's Medical University, Tokyo, Japan.
Insights
Prognostic factors for Panayiotopoulos syndrome were studied in 79 children. Pre-existing neurobehavioral disorders are linked to more frequent, pharmacoresistant seizures, but remission occurs by age 12.
Area of Science:
- Neurology
- Pediatric Epilepsy
Background:
- Panayiotopoulos syndrome is a common childhood epilepsy syndrome.
- Understanding prognostic factors is crucial for patient management.
Purpose of the Study:
- To identify prognostic factors associated with frequent seizure recurrences in Panayiotopoulos syndrome.
- To investigate the role of neurobehavioral disorders in seizure frequency and treatment response.
Main Methods:
- Retrospective analysis of medical records and electroencephalograms of 79 children with Panayiotopoulos syndrome.
- Classification of patients into typical, borderline, and atypical groups based on seizure recurrence frequency.
- Analysis of various clinical and demographic factors, including neurobehavioral disorders.
Main Results:
- A significant association was found between pre-existing neurobehavioral disorders and a higher frequency of seizures (>10 times) in the atypical group.
- Patients with Panayiotopoulos syndrome and mild neurobehavioral disorders exhibited pharmacoresistant seizures that recurred frequently.
- All patients achieved seizure remission by 12 years of age.
Conclusions:
- Pre-existing neurobehavioral disorders are a significant prognostic factor for frequent, pharmacoresistant seizures in Panayiotopoulos syndrome.
- Despite potential for frequent recurrences, Panayiotopoulos syndrome generally has a favorable long-term prognosis with seizure remission by adolescence.
- Surgical evaluation is typically not indicated for patients with Panayiotopoulos syndrome.
Abstract:
Prognostic factors for frequent seizure recurrences were studied in patients with Panayiotopoulos syndrome. The subjects were 79 children fulfilling the criteria of Panayiotopoulos syndrome who were monitored for longer than 2 years. Medical records and electroencephalograms were analyzed retrospectively. The total number of seizures in each patient at the final follow-up ranged from 1 to 22. The 79 patients were classified into three groups: typical Panayiotopoulos syndrome (seizure recurrence = 1-5 times, n = 45), borderline (6-9 times, n = 16), and atypical (>10 times, n = 18). Data analyzed included family history of seizure disorders, peri- and postnatal complications, previous seizure histories, age at epilepsy onset, clinical seizure manifestations, the frequency of status epilepticus, interictal electroencephalographic patterns, and the possible association of neurobehavioral disorders among the three groups. An association with pre-existing neurobehavioral disorders was significantly more frequent in the atypical than in the typical group (P < 0.05), but not significantly different between the typical and borderline or between the borderline and atypical patients (P> 0.05). In patients with Panayiotopoulos syndrome and pre-existing mild neurobehavioral disorders, seizures tend to be pharmacoresistant and to repeat more than 10 times. However, all patients experience seizure remission by 12 years of age, and should not be evaluated for surgery.
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