Autosomal Dominant Nocturnal Frontal Lobe Epilepsy

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Autosomal dominant nocturnal frontal lobe epilepsy. A distinctive clinical disorder.

The disorder of autosomal dominant nocturnal frontal lobe epilepsy has recently been identified, and is now delineated in detail. A phenotypically homogeneous group of five families from Australia, Britain and Canada, containing 47 affected individuals, was studied. The largest family contained 25 affected individuals spanning six generations. This disorder is characterized by clusters of brief...

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Nocturnal frontal lobe epilepsy

The paroxysmal motor events during sleep are certainly common.The systematic use of nocturnal video-polysomnography has largely improved the diagnostic yield in patients with clusters of nocturnal motor events. Two broad nosological categories have been identified: parasomnias (sleep terror and sleep-walking), which are thought to represent disorders of arousal during sleep,and the epileptic se...

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The role of nicotinic acetylcholine receptors in autosomal dominant nocturnal frontal lobe epilepsy

Autosomal dominant nocturnal frontal lobe epilepsy (ADNFLE) is a focal epilepsy with attacks typically arising in the frontal lobe during non-rapid eye movement (NREM) sleep. It is characterized by clusters of complex and stereotyped hypermotor seizures, frequently accompanied by sudden arousals. Cognitive and psychiatric symptoms may be also observed. Approximately 12% of the ADNFLE families c...

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Symptomatic nocturnal frontal lobe epilepsy

Nocturnal frontal lobe epilepsy (NFLE) is a disorder characterised by clusters of brief motor seizures during sleep, often without surface EEG epileptiform abnormalities’“. For these reasons, the prevalence of this disorder has probably been underestimated. Moreover, in the past, many patients with clusters of nocturnal motor attacks have been diagnosed as having nocturnal paroxysmal dystonia5,...

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O5: Frontal Lobe Epilepsy

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ژورنال

عنوان ژورنال: Epilepsia

سال: 2000

ISSN: 0013-9580,1528-1167

DOI: 10.1111/j.1528-1157.2000.tb00298.x