Literature DB >> 19469840

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

Salvatore Striano1, Giuseppe Capovilla, Vito Sofia, Antonino Romeo, Guido Rubboli, Pasquale Striano, Dorothée Kasteleijn-Nolst Trenité.   

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.

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Year:  2009        PMID: 19469840     DOI: 10.1111/j.1528-1167.2009.02114.x

Source DB:  PubMed          Journal:  Epilepsia        ISSN: 0013-9580            Impact factor:   5.864


  11 in total

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6.  Case Report: A Case of Eyelid Myoclonic Status With Tonic-Clonic Seizure and Literature Review.

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Review 10.  Candidate Genes for Eyelid Myoclonia with Absences, Review of the Literature.

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