LGS

E939685

LGS is a severe, childhood-onset epileptic encephalopathy characterized by multiple types of seizures, cognitive impairment, and a distinctive EEG pattern.

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Observed surface forms (1)

Surface form Occurrences
Lennox–Gastaut syndrome 0

Statements (53)

Predicate Object
instanceOf epileptic encephalopathy
neurological disorder
rare disease
affects both males and females
children
canBeIdiopathic true
hasAbbreviation LGS NERFINISHED
hasCause central nervous system infections
cortical malformations
genetic disorders
hypoxic–ischemic encephalopathy
perinatal brain injury
structural brain abnormalities
tuberous sclerosis complex NERFINISHED
hasCourse chronic
treatment-resistant
hasEEGPattern paroxysmal fast activity in sleep
slow spike-and-wave discharges
hasICD10Code G40.4
hasIncidence rare
hasOnset childhood
hasPrognosis high risk of persistent seizures into adulthood
often poor
hasSeizureType atonic seizures
atypical absence seizures
focal seizures
generalized tonic–clonic seizures
myoclonic seizures
tonic seizures
hasSymptom behavioral problems
developmental delay
frequent falls due to drop attacks
intellectual disability
isAssociatedWith autism spectrum disorder
behavioral dysregulation
sleep disturbances
status epilepticus
isCharacterizedBy cognitive impairment
distinctive EEG pattern
multiple seizure types
isTreatedWith cannabidiol
clobazam
corpus callosotomy
felbamate
ketogenic diet
lamotrigine
rufinamide NERFINISHED
topiramate
vagus nerve stimulation
valproate
namedAfter Henri Gastaut NERFINISHED
William G. Lennox NERFINISHED
typicalAgeOfOnset between 3 and 5 years

Referenced by (1)

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