Benign Movement Disorders Mimicking Seizures in Children: A Retrospective Cohort Study
1Pediatric Neurology Clinic, Balıkesir Atatürk City Hospital, Balıkesir 10100, Türkiye.
Insights
Developmental and benign movement disorders (DBMD) are frequently misdiagnosed in children with suspected seizures. Recognizing DBMD patterns can improve diagnosis and avoid unnecessary treatments.
Area of Science:
- Pediatric Neurology
- Child Neurology
- Movement Disorders
Background:
- Developmental and benign movement disorders (DBMD) are a common, yet often under-recognized, reason for pediatric referrals for suspected seizures.
- Misdiagnosis of DBMD can lead to inappropriate treatments and investigations in children.
Purpose of the Study:
- To determine the prevalence of DBMD in children evaluated for suspected seizures.
- To analyze the clinical characteristics, diagnostic patterns, and electroencephalography (EEG) findings in children with DBMD.
Main Methods:
- Retrospective cohort study of 453 children evaluated for suspected seizures (January 2019-January 2024).
- Exclusion of patients with epilepsy, cerebral palsy, metabolic disorders, developmental delay, psychiatric conditions, or brain abnormalities.
- Diagnosis of DBMD in 113 patients based on clinical evaluation and established criteria.
Main Results:
- DBMD prevalence was 24.9% (95% CI: 21.2-29.1), affecting nearly one in four referred children.
- Breath-holding spells were most common (26.5% of DBMD cases), followed by Sandifer syndrome and non-epileptic staring episodes.
- EEG was normal in 80.5% of DBMD patients; no epilepsy developed during follow-up.
Conclusions:
- DBMD represents a significant portion of pediatric seizure referrals.
- Identifying age-specific DBMD patterns and normal EEG findings can enhance diagnostic accuracy.
- Improved recognition of DBMD can prevent unnecessary investigations and antiepileptic drug prescriptions.
Abstract:
Background: Developmental and benign movement disorders (DBMD) are a common but often under-recognized cause of referral in children with suspected seizures, frequently leading to misdiagnosis and unnecessary treatment. Methods: This retrospective cohort study included 453 children evaluated for suspected seizures between January 2019 and January 2024. Patients with epilepsy, cerebral palsy, metabolic disorders, significant developmental delay, psychiatric conditions, or structural brain abnormalities were excluded. DBMD was diagnosed in 113 patients based on clinical evaluation by experienced pediatric neurologists and established diagnostic criteria. Demographic characteristics, diagnostic distribution, age at presentation, and electroencephalography (EEG) findings were analyzed. Prevalence was calculated with 95% confidence intervals (CIs). Group comparisons were performed using chi-square tests and one-way ANOVA with Tukey post hoc analysis. Results: The prevalence of DBMD was 24.9% (95% CI: 21.2-29.1), corresponding to nearly one in four children referred with suspected seizures. Breath-holding spells were the most common diagnosis (6.6% of the total cohort; 26.5% of DBMD cases), followed by Sandifer syndrome and non-epileptic staring episodes. Age at presentation differed significantly between diagnostic groups (p = 0.001), with breath-holding spells occurring at younger ages and staring episodes at older ages. EEG findings were normal in 80.5% of patients, and no diagnosis-specific epileptiform patterns were identified. No patients were observed to develop epilepsy during the follow-up period. Conclusions: DBMD accounts for a substantial proportion of children referred for suspected seizures. Recognition of age-specific clinical patterns and predominantly normal EEG findings may improve diagnostic accuracy and help avoid unnecessary investigations and antiepileptic treatment.
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