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Rolandic epilepsy (RE) or childhood benign epilepsy with central temporal spikes (BECT) is the most common idiopathic partial epilepsy syndrome in children, where "idiopathic" means genetic predisposition
.
Although it has long been believed that RE has a genetic component, clinical and genetic studies have shown complex inheritance patterns
Rolandic epilepsy (RE) or childhood benign epilepsy with central temporal spikes (BECT) is the most common idiopathic partial epilepsy syndrome in children, where "idiopathic" means genetic predisposition
An 18-year-old woman was admitted to the hospital for focal epilepsy
.
A series of MRI examinations showed migrating Roland lesions (Figure AD).
An 18-year-old woman was admitted to the hospital for focal epilepsy
(A) FLAIR head imaging examination performed by the patient 1 year ago
(A) FLAIR head imaging examination performed by the patient 1 year ago(B) The small damage on the left Rolandic cortex disappeared after 2 months and reappeared after 9 months (C)
(B) The small damage on the left Rolandic cortex disappeared after 2 months and reappeared after 9 months (C)(D) A similar minor injury subsequently occurred in the right Rolandic cortex
(D) A similar minor injury subsequently occurred in the right Rolandic cortex
Literature source: https://n.
Literature source: https://n.
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