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http://dx.doi.org/10.14253/acn.2018.20.1.36

Lennox-Gastaut syndrome associated with dysgenesis of corpus callosum

Janati, A. Bruce (Department of Neurology, Center for Neurology)
ALGhasab, Naif Saad (Department of Internal Medicine, King Faisal Specialist Hospital, Hail University)
Umair, Muhammad (Dow Medical College)
FazelHaq, FazelHaq (Department of Internal Medicine, King Khaled Hospital)
Osman, Aboubaker (Department of Internal Medicine, King Khaled Hospital)
Sammour, Mohammad (Department of Pediatrics, King Khaled Hospital)
Ahmed, AmalAbdulgadir (Department of Pediatrics, King Khaled Hospital)
Ghorbel, Sofiane (Center for Rehabilitation, King Khaled Hospital)
Alshammeri, Hesse (Department of Internal Medicine, King Khaled Hospital)
Aldaife, Maram (Department of Internal Medicine, King Khaled Hospital)
Abdollah, Ahmad (Department of Internal Medicine, King Khaled Hospital)
ALMubaddel, Afnan Ibrahim (Autism and Behavioral Disorder at King Faisal Specialist Hospital and Research Center)

Publication Information

Annals of Clinical Neurophysiology / v.20, no.1, 2018 , pp. 36-40 More about this Journal

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.

Keywords

Epilepsy; Slow spike-wave complexes; Secondary bilateral synchrony;

Citations & Related Records

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