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Lennox-Gastaut syndrome
(redirected from Lennox syndrome)

   Also found in: Wikipedia 0.04 sec.
Len·nox-Gas·taut syndrome (lnks-g-st, -gä-)
n.
A generalized myoclonic astatic epilepsy that occurs in children as a result of various cerebral afflictions such as perinatal hypoxia, cerebral hemorrhage, encephalitis, and maldevelopment or metabolic disorders of the brain; it is characterized by mental retardation and generalized tonic seizures or akinetic attacks. Also called Lennox syndrome.

Lennox-Gastaut syndrome Lennox syndrome Neurology A severe encephalopathic form of epilepsy that constitutes 5% of all childhood epilepsies Clinical Early onset of multiple types–eg, absence, atonic, and others of seizures, slow spike-wave EEG pattern, cerebral atrophy, and often progressive mental retardation; seizures are poorly controlled even with multiple anticonvulsants Prognosis For cognitive development, poor; felbamate may ↓ Sx. See Felbamate.


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