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Epilepsy-Aphasia Spectrum: From Landau-Kleffner Sy ndrome to Rolandic Epilepsy (Hardcover)
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Epilepsy-Aphasia Spectrum: From Landau-Kleffner Sy ndrome to Rolandic Epilepsy (Hardcover)
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Landau-Kleffner syndrome (LKS) is a rare childhood neurological
syndrome. It is characterised by a sudden or gradual loss of
ability to understand of express language (aphasia) and usually
occurs in children between the ages of 3 and 7 years. Rolandic
epilepsy is the most common epilepsy syndrome in childhood with
involvement of the oropharyngeal manifestations, hypersalivation
and arrest of speech. These two syndromes are considered to be
aspects of the epilepsy-aphasia spectrum with common rolandic
epilepsy being the mildest form and LKS the most severe.
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