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Rolandic epilepsy: Difference between revisions
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Benign Rolandic epilepsy or benign childhood epilepsy with centrotemporal spikes ( | Benign Rolandic epilepsy or benign childhood epilepsy with centrotemporal spikes ([[BECTS]]) 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)<ref>[https://en.wikipedia.org/w/index.php?title=Rolandic_epilepsy&oldid=679036413 wikipedia:Rolandic epilepsy]</ref> | ||
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[[Category:Neurological disorder]] | |||
Latest revision as of 14:24, 13 October 2018
Benign Rolandic epilepsy or benign childhood epilepsy with centrotemporal spikes (BECTS) 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]
Links
Las evoluciones atípicas de la epilepsia rolándica son complicaciones predecibles
Rolandic epilepsy and dyslexia
Panayiotopoulos syndrome