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Assessment of Blink Reflex in Genetic Generalized Epilepsy Patients With Eyelid Myoclonia.

Abstract
Eyelid myoclonia (EM) with or without absences are a rare type of generalized seizures associated with a variety of epilepsy syndromes with an unknown pathophysiology. The aim of this study was to investigate the possible contribution of the brainstem structures in this underrecognized special type of seizures. Sixteen consecutive patients with EM, diagnosed with genetic generalized epilepsy (GGE) according to International League Against Epilepsy 2010 criteria were included. Brainstem excitabilities were examined by blink reflex (BR) studies. The results of BR studies in GGE patients with EM were statistically compared with 2 control groups; namely age- and gender-matched healthy volunteers and juvenile myoclonic epilepsy (JME) patients without any absences and using similar antiepileptic drugs. There were no statistical differences between the thresholds of the BR studies and the BR recovery curves in terms of amplitudes and areas of healthy subjects, JME patients and GGE patients with EM. Our findings do not support a profound interictal hyperexcitability in the BR-related brainstem structures of the GGE patients with EM. It can be considered that EM may be associated with excitability changes of the occipital cortex and other cortical areas.
AuthorsGüneş Altıokka-Uzun, Esme Ekizoğlu, Elif Kocasoy-Orhan, Nerses Bebek, Candan Gürses, Ayşen Gökyiğit, Ali Emre Öge, Betül Baykan
JournalClinical EEG and neuroscience (Clin EEG Neurosci) Vol. 48 Issue 2 Pg. 118-122 (Mar 2017) ISSN: 2169-5202 [Electronic] United States
PMID27170670 (Publication Type: Journal Article)
Topics
  • Adolescent
  • Adult
  • Blinking
  • Brain Stem (physiopathology)
  • Epilepsies, Myoclonic (physiopathology)
  • Epilepsy, Generalized (physiopathology)
  • Eyelid Diseases (physiopathology)
  • Female
  • Humans
  • Male
  • Myoclonus (physiopathology)
  • Young Adult

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