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Eyelid myoclonia with absences (Jeavons syndrome): A well‐defined idiopathic generalized epilepsy syndrome or a spectrum of photosensitive conditions?

Striano, Salvatore, Capovilla, Giuseppe, Sofia, Vito, Romeo, Antonino, Rubboli, Guido, Striano, Pasquale, Trenité, Dorothée Kasteleijn‐Nolst·2009·Epilepsia

Abstract

Summary: 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.

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Metadata

Authors
Striano, S., Capovilla, G., Sofia, V., Romeo, A., Rubboli, G., Striano, P., & Trenité, D. K.
Venue
Epilepsia
Publisher
Wiley
Published
2009-05
Volume
50
Issue
s5
Pages
15-19
ISSN
  • 0013-9580 (ISSN-L)
  • 1528-1167
OpenAlex
W2153668324
Cited by
174
References
0
FWCI
3.88
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Eyelid myoclonia with absences (Jeavons syndrome): A well‐defined idiopathic generalized epilepsy syndrome or a spectrum of photosensitive conditions? https://app.cochat.ai/papers/10.1111/j.1528-1167.2009.02114.x
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Striano, S., Capovilla, G., Sofia, V., Romeo, A., Rubboli, G., Striano, P., & Trenité, D. K. (2009). Eyelid myoclonia with absences (Jeavons syndrome): A well‐defined idiopathic generalized epilepsy syndrome or a spectrum of photosensitive conditions? Epilepsia. https://doi.org/10.1111/j.1528-1167.2009.02114.x

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

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