Erschienen in:
01.08.2014 | Journal club
Narcolepsy: environment, genes and treatment
verfasst von:
K. J. Peall, N. P. Robertson
Erschienen in:
Journal of Neurology
|
Ausgabe 8/2014
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Excerpt
Narcolepsy is a central sleep disorder typically involving symptoms of daytime somnolence, unintentional lapses into sleep, sleep paralysis and frequent nocturnal awakenings. The disorder involves a dissociated sleep-wake cycle with rapid eye movement (REM) sleep intruding into wakefulness. Narcolepsy with cataplexy (type 1 narcolepsy) is caused by loss of hypocretin-secreting neurons, decreasing CSF levels of this neuropeptide. Mean prevalence is believed to be 30/100,000, with the highest rates observed in Japan and the lowest in Saudia Arabia. Age at onset is typically 10–30 years, peaking at 15 years and rarely presenting <10 years and >40 years of age. …