Lennox-Gastaut Syndrome (Childhood Epileptic Encephalopathy)

Research output: Contribution to journalReview article

117 Citations (Scopus)

Abstract

Lennox-Gastaut syndrome (LGS) is a childhood epileptic encephalopathy characterized by an electroclinical triad of generalized slow spike wave (SSW) activity in the EEG, multiple types of epileptic seizures, and slow mental development. It is usually subdivided into symptomatic and cryptogenic types, the latter accounting for at least one fourth of all patients. Symptomatic cases are due to diverse cerebral conditions, which are usually bilateral, diffuse, or multifocal, involving cerebral gray matter. Twenty percent of all patients with LGS have prior infantile spasms with hypsarrythmia. The characteristic interictal EEG pattern of LGS is 1.5 to 2.5 Hz SSW activity, which is bilaterally synchronous, dominant over the frontocentral regions, and usually symmetric. There are varying degrees of slowing of the background. Sleep discloses paroxysms of generalized fast (10 to 25 Hz) rhythmic activity.

Original languageEnglish (US)
Pages (from-to)426-441
Number of pages16
JournalJournal of Clinical Neurophysiology
Volume20
Issue number6
DOIs
StatePublished - Dec 1 2003

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Brain Diseases
Electroencephalography
Infantile Spasms
Epilepsy
Sleep
Lennox Gastaut Syndrome

Keywords

  • Epileptic encephalopathies
  • Independent multifocal spike discharges
  • Paroxysmal fast activity
  • Slow spike wave activity
  • Tonic and atonic seizures

ASJC Scopus subject areas

  • Clinical Neurology
  • Physiology
  • Neuroscience(all)

Cite this

Lennox-Gastaut Syndrome (Childhood Epileptic Encephalopathy). / Markand, Omkar N.

In: Journal of Clinical Neurophysiology, Vol. 20, No. 6, 01.12.2003, p. 426-441.

Research output: Contribution to journalReview article

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