Affiliations 

  • 1 Department of Neurology, Xijing Hospital, Fourth Military Medical University, Xi'an 710032, PR China
  • 2 Department of Aerospace Physiology, Fourth Military Medical University, Xi'an 710032, PR China
  • 3 Neuroscience Institute, Kuala Lumpur Hospital, Malaysia. Electronic address: drswabengwei@gmail.com
  • 4 Department of Neurology, Xijing Hospital, Fourth Military Medical University, Xi'an 710032, PR China. Electronic address: liuyhong@fmmu.edu.cn
Epilepsy Behav, 2014 Mar;32:64-71.
PMID: 24495864 DOI: 10.1016/j.yebeh.2013.12.016

Abstract

Jeavons syndrome (JS) is one of the underreported epileptic syndromes and is characterized by eyelid myoclonia (EM), eye closure-induced seizures or electroencephalography (EEG) paroxysms, and photosensitivity. In the Western populations, it has been reported to be characterized by focal posterior, occipital predominant epileptiform discharges (OPEDs) or frontal predominant epileptiform discharges (FPEDs) followed by generalized EDs in both interictal and ictal EEG recordings. However, it is not clear if there are different clinical manifestations between OPEDs and FPEDs. The clinical and electrographic presentations in the Chinese population are largely unknown. Here, we report the clinical and electroencephalographic features of 50 Chinese patients with JS and evaluate for the presence of different clinical features between patients with OPEDs and patients with FPEDs.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.