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Benign rolandic epilepsy (BRE)
Other Names for this Disease
- Benign epilepsy of childhood with centrotemporal spikes (BECCT)
- Benign epilepsy with centro-temporal spikes (BECTS)
- Benign rolandic epilepsy of childhood (BREC)
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 This form of epilepsy is characterized by seizures involving the part of the frontal lobe of the brain called the rolandic area. The seizures associated with this condition typically occur during the nighttime.  Treatment is usually not prescribed, since the condition tends to disappear by puberty. Benign rolandic epilepsy is the most common form of childhood epilepsy. It is referred to as "benign" because most children outgrow the condition by puberty, usually by 14 years of age.
Last updated: 5/6/2008
- Blumstein MD, Friedman MJ. Childhood Seizures. Emerg Med Clin N Am. 2007;
- Fountain NB. Evidence for Functional Impairment But Not Structural Disease in Benign Rolandic Epilepsy. Epilepsy Curr. 2008 January ;
- Benign rolandic epilepsy. Epilepsy Action. March 14, 2007; http://www.epilepsy.org.uk/info/benign.html. Accessed 5/6/2008.
- MedlinePlus was designed by the National Library of Medicine to help you research your health questions, and it provides more information about this topic. Click on the link to view this information.
- The Epilepsy Foundation has an information page on benign rolandic epilepsy. Click on Epilepsy Foundation to view the information page.
In Depth Information
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- The Online Mendelian Inheritance in Man (OMIM) database contains genetics resources that discuss Benign rolandic epilepsy (BRE). Click on the link to go to OMIM and review these resources.
- PubMed is a searchable database of medical literature and lists journal articles that discuss Benign rolandic epilepsy (BRE). Click on the link to view a sample search on this topic.