Difference between revisions of "Lennox Gastaut Syndrome"

From EEGpedia
Jump to: navigation, search
(Created page with "==Background== * Severe seizures in childhood * Presentation before eight years of age, most commonly between three and five years of age * Many cases evolve into Lennox Gasta...")
 
 
(One intermediate revision by the same user not shown)
Line 18: Line 18:
  
 
==EEG==  
 
==EEG==  
* Spike-and-wave superimposed on an abnormal, slow background.
+
* [[Spike slow wave complex]] superimposed on an abnormal, slow background.
* The [[Spike slow wave complex]] and [[Sharp wave slow wave complex]] are generalized at a frequency of 1.5 to 2.5 Hz (slow)
+
* The [[Spike slow wave complex]] and [[Sharp wave slow wave complex]] are generalized at a frequency of 1.5 to 2.5 Hz (slow), usually with the highest amplitude frontal.
 
* Transient and shifting asymmetries are frequent
 
* Transient and shifting asymmetries are frequent
 
* Non-REM sleep increases the discharges. In REM sleep the discharges decreases.
 
* Non-REM sleep increases the discharges. In REM sleep the discharges decreases.
Line 33: Line 33:
 
* Valproic acid, lamotrigine, topiramate, rufinamide, felbamate, and clobazam can be effective
 
* Valproic acid, lamotrigine, topiramate, rufinamide, felbamate, and clobazam can be effective
 
* Carbamazepine can worsen the drop attacks
 
* Carbamazepine can worsen the drop attacks
 +
 +
 +
----
 +
 +
'''''Lennox gastaut in a 3 years and 10 months old boy (source) with multiple spike and slow waves and a slow basic rhythm'''''
 +
[[File:Lennox_gastaut_in_a_3_years_and_10_months_old_boy_(source)_EEGpedia.png|border|none|1200px|left]]
 +
 +
 +
----

Latest revision as of 16:16, 4 August 2017

Background

  • Severe seizures in childhood
  • Presentation before eight years of age, most commonly between three and five years of age
  • Many cases evolve into Lennox Gastaut from other epilepsy syndromes, particularly West Syndrome (Infantile Spasm)

Clinics

  • Mixture of seizure types
    • Tonic
    • Tonic-clonic
    • Atonic (drop attacks)
    • Myoclonic
    • atypical absences
  • Brief tonic seizures of seconds to 1 minute.
  • The seizures can cause falls.
  • Eyelid retraction, staring, mydriasis, and apnea are commonly associated
  • The seizures are frequent
  • Mental retardation before seizure onset in 20-60%

EEG

  • Spike slow wave complex superimposed on an abnormal, slow background.
  • The Spike slow wave complex and Sharp wave slow wave complex are generalized at a frequency of 1.5 to 2.5 Hz (slow), usually with the highest amplitude frontal.
  • Transient and shifting asymmetries are frequent
  • Non-REM sleep increases the discharges. In REM sleep the discharges decreases.
  • Hyperventilation or photic stimulation does not trigger the discharges.


Ictal EEG

  • Tonic seizure: typically fast rhythmic discarges of 10 – 20 Hz, increasing in amplitude.
  • Myoclonic seizures: bursts of arrhythmic, multiple spike-wave or irregular spike-wave activity
  • Atypical absence seizures: Slow (<2.5 Hz) and often asymmetric and irregular spike-and-wave activity

Treatment

  • No drug is highly effective
  • Valproic acid, lamotrigine, topiramate, rufinamide, felbamate, and clobazam can be effective
  • Carbamazepine can worsen the drop attacks



Lennox gastaut in a 3 years and 10 months old boy (source) with multiple spike and slow waves and a slow basic rhythm

Lennox gastaut in a 3 years and 10 months old boy (source) EEGpedia.png