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Benign rolandic epilepsy of childhood

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Benign Rolandic epilepsy (BRE), also called benign epilepsy with centrotemporal spikes (BECTS) or benign epilepsy of childhood with centrotemporal spikes (BECCT) is the most common epilepsy syndrome in children (1,2):

  • seizures originate in the Rolandic area of the brain (situated around the central sulcus of the brain, also called as centrotemporal area, located around the Rolandic fissure) (2)

  • most of the affected children usually outgrow this condition by puberty, hence the term "benign”
    • typically occurs in children aged seven to ten, but may start as young as three years of age, and is twice as common in boys (1)

  • incidence of BRE is 10 to 20 per 100,000 children up to age 15 years (2)
    • makes up about 15% of all epilepsy cases in children
    • adults are not affected

  • speech dyspraxia and language impairments are frequent comorbidities predating the onset of seizures (1)
    • is a six times higher odds of dyslexia, which should be anticipated at diagnosis and during routine follow-up

  • there is often a family history of speech and language disorders
    • Benign Rolandic epilepsy (BRE) is classified as a genetic disorder as approximately 25% of patients have a family history of either febrile seizures or epilepsy (2)

  • seizure remission is universal by the age of 15 although a small but elevated risk of epilepsy in adult life remains and the risk of migraine is also increased (1,2)
    • seizures occur for only 2 to 4 years and spontaneously resolve by the age of 15 to 16 years (in more than 95% of children) (2)
    • majority of the patients have less than 10 seizures, 10% to 20% having only one seizure in their lifetime (2)
    • if early seizure onset then associated with a higher number of seizures and/or a prolonged period of seizure activity
    • if early seizure onset then this is also known to cause cognitive, behavioral, and speech abnormalities which resolve by adolescence along with resolution of seizures
    • note that BRE can be an early presentation of other epileptic syndromes

Download free parental guide from https://childhoodepilepsy.org.

Reference

  1. Fisher RS, Cross JH, French JA, et al. Operational classification of seizure types by the International League Against Epilepsy: position paper of the ILAE Commission for Classification and Terminology. Epilepsia. 2017 Apr;58(4):522-30.
  2. Amrutkar CV, Riel-Romero RM. Rolandic Epilepsy Seizure. [Updated 2023 Aug 7]. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2026 Jan-.

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