Pediatric Narcolepsy: A Brief Report.

Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F62690094%3A18450%2F17%3A50013677" target="_blank" >RIV/62690094:18450/17:50013677 - isvavai.cz</a>
Alternative codes found
RIV/00216208:11150/18:10368609 RIV/00179906:_____/18:10368609
Result on the web
<a href="http://dx.doi.org/10.1177/0009922817732149" target="_blank" >http://dx.doi.org/10.1177/0009922817732149</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1177/0009922817732149" target="_blank" >10.1177/0009922817732149</a>

Result language
angličtina
Original language name
Pediatric Narcolepsy: A Brief Report.
Original language description
Narcolepsy is a chronic but nonprogressive neurological disorder that is characterized by poor control of sleepwake cycles. Currently, there are 2 types of narcolepsy: type 1 narcolepsy with cataplexy and reduced cerebral spinal fluid hypocretin levels and type 2 narcolepsy without cataplexy and reduced cerebral spinal fluid hypocretin levels.1 The onset of narcolepsy is already in childhood, between the ages of 7 and 25,2 but it usually takes 8 to 10 years before this disorder is diagnosed due to the comorbid conditions of other neurological diseases whose symptoms also include some sleeping isorders.3 The purpose of this study was to report on an exemplary case of a child narcolepsy whose early, thorough diagnosis could lead to the early management and treatment of this incurable rare neurological disorder.
Czech name
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Czech description
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Project
—
Continuities
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Publication year
2017
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

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