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Rolandic epilepsy: Difference between revisions
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[http://www.ncbi.nlm.nih.gov/pubmed/26178515 Las evoluciones atípicas de la epilepsia rolándica son complicaciones predecibles] | [http://www.ncbi.nlm.nih.gov/pubmed/26178515 Las evoluciones atípicas de la epilepsia rolándica son complicaciones predecibles] | ||
[http://www.cjcp.org/EN/abstract/abstract13677.shtml# Relationship between Panayiotopoulos syndrome and Rolandic epilepsy and the prognosis of Panayiotopoulos syndrome] | |||
<references/> | <references/> | ||
Revision as of 23:55, 17 October 2015
Benign Rolandic epilepsy or benign childhood epilepsy with centrotemporal spikes (BCECTS) is the most common epilepsy syndrome in childhood. Most children will outgrow the syndrome (it starts around the age of 3-13 with a peak around 8–9 years and stops around age 14-18), hence the label benign. The seizures, sometimes referred to as sylvian seizures, start around the central sulcus of the brain (also called the centrotemporal area, located around the Rolandic fissure, after Luigi Rolando)[1]
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Las evoluciones atípicas de la epilepsia rolándica son complicaciones predecibles