Abstract
Eyelid myoclonia with absences (EMA), or Jeavons syndrome, is a generalized epileptic condition clinically characterized by eyelid myoclonia (EM) with or without absences, eye closure-induced electroencephalography (EEG) paroxysms, and photosensitivity; in addition, rare tonic-clonic seizures may also occur. Although first described in 1977 and widely reported by several authors within the last few years, EMA has not been yet recognized as a definite epileptic syndrome. However, when strict criteria are applied to the diagnosis, EMA appears to be a distinctive condition that could be considered a myoclonic epileptic syndrome, with myoclonia limited to the eyelids, rather than an epileptic syndrome with absences. © 2009 International League Against Epilepsy.
Author supplied keywords
Cite
CITATION STYLE
Striano, S., Capovilla, G., Sofia, V., Romeo, A., Rubboli, G., Striano, P., & Trenité, D. K. N. (2009). Eyelid myoclonia with absences (Jeavons syndrome): A well-defined idiopathic generalized epilepsy syndrome or a spectrum of photosensitive conditions? Epilepsia, 50(SUPPL. 5), 15–19. https://doi.org/10.1111/j.1528-1167.2009.02114.x
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.