The Landau-Kleffner syndrome or the syndrome of acquired epileptic aph
asia was first described in 1957. The disorder is characterised by gra
dual or rapid loss of language in a previously normal child. All child
ren have abnormal EEG compatible with the diagnosis of epilepsy, howev
er, only 70% have clinical seizures. The present article presents a re
view of the current knowledge concerning this disorder. Information is
provided related to the clinical picture, etiology, pathogenesis, tre
atment and outcome.