Lennox-Gastaut syndrome associated with dysgenesis of corpus callosum |
A.Bruce Janati1, Naif Saad ALGhasab2, Muhammad Umair3, FazelHaq 4, Aboubaker Osman4, Mohammad Sammour5, AmalAbdulgadir Ahmed5, Sofiane Ghorbel6, Hesse Alshammeri4, Maram Aldaife4, Ahmad Abdollah4, and Afnan Ibrahim ALMubaddel7 |
1Department of Neurology, Center for Neurology, Fairfax, VI, USA 2Department of Internal Medicine, King Faisal Specialist Hospital, Hail University, Riyadh, Kingdom of Saudi Arabia 3Dow Medical College, Karachi, Pakistan 4Department of Internal Medicine, King Khaled Hospital, Hail, Kingdom of Saudi Arabia 5Department of Pediatrics, King Khaled Hospital, Hail, Kingdom of Saudi Arabia 6Center for Rehabilitation, King Khaled Hospital, Hail, Kingdom of Saudi Arabia 7Speclaist in Autism and Behavioral Disorder at King Faisal Specialist Hospital and Research Center, Riyadh, Kingdom of Saudi Arabia |
Corresponding Author:
Naif Saad ALGhasab ,Tel: +966-507886878 , Fax: +966-165397403 , Email: dr.legend@hotmail.com |
Received March 4, 2017 Revised: December 25, 2017 Accepted December 27, 2017 |
Copyright © 2018 The Korean Society of Clinical Neurophysiology |
This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium,
provided the original work is properly cited. |
ABSTRACT |
Lennox-Gastaut syndrome (LGS) is an electro-clinical syndrome composed of the triad of mental retardation, multiple seizure types, and the characteristic generalized slow spike-wave complexes in the electroencephalogram. In this article, we report on two patients with LGS whose brain magnetic resonance imaging showed dysgenesis of corpus callosum (CC). We discuss the role of CC in the genesis of secondary bilateral synchrony. |
Key words:
Epilepsy; Slow spike-wave complexes; Secondary bilateral synchrony |
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