Landau-Kleffner Syndrome

Rotenberg, Joshua S.; Pearl, Phillip L.

doi:10.1001/archneur.60.7.1019

Cited by 18 publications

(9 citation statements)

References 12 publications

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“…Sleep EEG may reveal continuous and diffuse slow spikes and waves, mainly at 1.5-2.5Hz persisting through all the slow-sleep stages. This pattern of continuous spikes and waves during slow sleep (CSWS) or electrical status epilepticus in sleep (ESES) in patients with LKS tends to be unilateral or clearly lateralized [9]. Our patient EEG pattern was similar to those features.…”

Section: Discussion:-supporting

confidence: 69%

Landau- Kleffner Syndrome: A Rare Case Report.

Surgeon¹,

Surgeon²,

SundaraRaju³

et al. 2017

IJAR

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Section: Discussion:-supporting

confidence: 69%

Landau- Kleffner Syndrome: A Rare Case Report.

Surgeon¹,

Surgeon²,

SundaraRaju³

et al. 2017

IJAR

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“…Patient 1: An example of stable cortical sources. In patient 3, involvement of Broca and Wernicke areas in the generation of IISs is well known in Landau-Kleffner syndrome (Rotenberg and Pearl, 2003). Right: magnetic fields and reconstructed cortical current density maps from 216 to 32 milliseconds (between left and right dashed lines for the duration of IIS and the dashed line in the middle marks the IIS peak as 0 millisecond).…”

Section: Discussionmentioning

confidence: 92%

Sparse MEG Source Imaging For Reconstructing Dynamic Sources of Interictal Spikes in Partial Epilepsy

Zhu

Zhang²,

Dickens³

et al. 2013

Journal of Clinical Neurophysiology

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“…29 Further, the 85% threshold is not uniformly adhered to across groups. 28 ESES is a characteristic EEG finding in Landau-Kleffner syndrome, 30,31 a syndrome characterized by auditory agnosia at the onset followed by an overall deterioration of language skills and other cognitive functions. However, ESES can be seen in outside of this specific syndrome.…”

Section: Epileptic Encephalopathiesmentioning

confidence: 99%

Serial Neuropsychological Evaluation of Children with Severe Epilepsy

2016

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Cognitive impairment is common in children and adolescents with epilepsy. Though there is increasing recognition that even children with more benign epilepsy syndromes may show cognitive loss over time, this is particularly true in children with severe epilepsies, termed the epileptic encephalopathies. The current article discusses general cognition in children with epilepsy, focusing on risk factors for cognitive decline over time in severe epilepsies. The ?epileptic encephalopathies? are briefly introduced and methods for assessing cognitive loss over time are discussed with an emphasis on the use of reliable change indices. The strengths and the limitations of this approach are noted as they pertain to children. The article concludes with an illustrative case example of a young child with a severe epilepsy syndrome and apparent cognitive loss. The utility and limitations of reliable change indices are discussed within the context of this case.

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Landau-Kleffner Syndrome

Cited by 18 publications

References 12 publications

Landau- Kleffner Syndrome: A Rare Case Report.

Landau- Kleffner Syndrome: A Rare Case Report.

Sparse MEG Source Imaging For Reconstructing Dynamic Sources of Interictal Spikes in Partial Epilepsy

Serial Neuropsychological Evaluation of Children with Severe Epilepsy

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