The disorder usually occurs in children between the ages of 3 and 7 years. There appears to be a male dominance in the diagnosis of the syndrome ratio of 1. While many affected individuals have clinical seizures, some only have electrographic seizures, including electrographic status epilepticus of sleep ESES. The first indication of the language problem is usually auditory verbal agnosia. This is demonstrated in patients in multiple ways including the inability to recognize familiar noises and the impairment of the ability to lateralize or localize sound.
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Landau e Frank R. Soprano et al. Epilepsy in children. New York: Raven Press, Neurol, v. Age of onset and outcome in acquired aphasia with convulsive disorder Landau-Kleffner. Dev Med Child Neurol, v. Acquired epileptiform aphasia in children Landau-Kleffner syndrome. Journal of Clinical Neurophysiology, v. Psicothema, v.
Acta Neurologica, Belgica, v. Treatment with subpial intracortical transection. Brain, v. Psicologia Conductual, v.
Acquired epileptic aphasia: neuropsychologic follow- up of 12 patients. Pediatric Neurology, v. The research regarding the performance speech-language pathology in patient carriers of the Landau-Kleffner syndrome, also call of acquired aphasia with epilepsy, is still constituted in a field not very explored by the Brazilian scientific community. Aim: To lift theoretical subsidies that propitiate to the speech-language a practical intervention in carriers of SLK. Conclusion: this scientific article of revision approaches the cause, historical, characteristics, comparisons and conclusions.
Especialista em Psicopedagogia Institucional.
Síndrome de Landau-Kleffner
Landau e Frank R. Soprano et al. Epilepsy in children. New York: Raven Press, Neurol, v.
Qué es el síndrome de Landau-Kleffner: causas, síntomas, tratamiento, pronóstico, recuperación
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Síndrome de Landau-Kleffner: síntomas, causas y tratamiento