Browse
Explore conditions, clinical trials, and the organisations running them.
Up to: Syndromic disease · Childhood-onset epilepsy syndrome · GRIN2A-related complex neurodevelopmental disorder
Landau-Kleffner syndrome
A rare form of epileptic encephalopathy with spike-wave activation in sleep (EE-SWAS) characterized by various combinations of acquired cognitive, language, behavioral, and motor deficits associated with marked spike- and- wave activation in sleep. In Landau-Kleffner syndrome, receptive language is mainly affected, with an acquired auditory verbal agnosia.
This condition has no sub-types.