Literature DB >> 18201664

Prader Willi Syndrome and excessive daytime sleepiness.

Danny Camfferman1, R Doug McEvoy, Fergal O'Donoghue, Kurt Lushington.   

Abstract

Prader Willi Syndrome (PWS) is a rare genetic disorder characterized by a range of physical, psychological and physiological abnormalities. PWS patients may also demonstrate a range of abnormalities of sleep architecture and of breathing during sleep, and excessive daytime sleepiness (EDS). In the general population EDS is associated with Obstructive Sleep Apnea Syndrome (OSAS). In PWS, by contrast, OSAS is unlikely to fully explain EDS and other factors, including hypothalamic dysfunction are likely to contribute. The present review examines OSAS and hypothalamic dysfunction and other contributing factors to EDS in PWS.

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Year:  2008        PMID: 18201664     DOI: 10.1016/j.smrv.2007.08.005

Source DB:  PubMed          Journal:  Sleep Med Rev        ISSN: 1087-0792            Impact factor:   11.609


  15 in total

Review 1.  Cellular and disease functions of the Prader-Willi Syndrome gene MAGEL2.

Authors:  Klementina Fon Tacer; Patrick Ryan Potts
Journal:  Biochem J       Date:  2017-06-16       Impact factor: 3.857

Review 2.  Sleep Disturbances in Neurodevelopmental Disorders.

Authors:  Althea Robinson-Shelton; Beth A Malow
Journal:  Curr Psychiatry Rep       Date:  2016-01       Impact factor: 5.285

Review 3.  A Comprehensive Guide to the MAGE Family of Ubiquitin Ligases.

Authors:  Anna K Lee; Patrick Ryan Potts
Journal:  J Mol Biol       Date:  2017-03-11       Impact factor: 5.469

4.  Establishing the content validity of the Epworth Sleepiness Scale for Children and Adolescents in Prader-Willi syndrome.

Authors:  Vanessa Perez Patel; Albena Patroneva; Daniel G Glaze; Krystle Davis Ms; Elizabeth Merikle; Amee Revana
Journal:  J Clin Sleep Med       Date:  2022-02-01       Impact factor: 4.062

5.  Pitolisant in an Adolescent with Prader-Willi Syndrome.

Authors:  Stephanie Pennington; Danielle Stutzman; Elise Sannar
Journal:  J Pediatr Pharmacol Ther       Date:  2021-05-19

6.  Narcolepsy and predictors of positive MSLTs in the Wisconsin Sleep Cohort.

Authors:  Aviv Goldbart; Paul Peppard; Laurel Finn; Chad M Ruoff; Jodi Barnet; Terry Young; Emmanuel Mignot
Journal:  Sleep       Date:  2014-06-01       Impact factor: 5.849

7.  Magel2, a Prader-Willi syndrome candidate gene, modulates the activities of circadian rhythm proteins in cultured cells.

Authors:  Julia Devos; Sara V Weselake; Rachel Wevrick
Journal:  J Circadian Rhythms       Date:  2011-12-30

8.  Prader-Willi syndrome: A primer for clinicians.

Authors:  Mary Cataletto; Moris Angulo; Gila Hertz; Barbara Whitman
Journal:  Int J Pediatr Endocrinol       Date:  2011-10-18

9.  Deletion of the Snord116/SNORD116 Alters Sleep in Mice and Patients with Prader-Willi Syndrome.

Authors:  Glenda Lassi; Lorenzo Priano; Silvia Maggi; Celina Garcia-Garcia; Edoardo Balzani; Nadia El-Assawy; Marco Pagani; Federico Tinarelli; Daniela Giardino; Alessandro Mauro; Jo Peters; Alessandro Gozzi; Graziano Grugni; Valter Tucci
Journal:  Sleep       Date:  2016-03-01       Impact factor: 5.849

10.  Prader-Willi syndrome, excessive daytime sleepiness, and narcoleptic symptoms: a case report.

Authors:  Sara V Weselake; Jessica L Foulds; Robert Couch; Manisha B Witmans; Daniela Rubin; Andrea M Haqq
Journal:  J Med Case Rep       Date:  2014-04-17
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