Effects of Growth Hormone Treatment on Sleep-Related Parameters in Adults With Prader-Willi Syndrome

CONTEXT: Prader-Willi syndrome (PWS) is a rare, genetic, multisymptom, neurodevelopmental disease due to lack of the expression of the paternal genes in the q11 to q13 region of chromosome 15. The main characteristics of PWS are muscular hypotonia, hyperphagia, obesity, behavioral problems, cognitiv...

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Detalles Bibliográficos
Autores principales: Shukur, Hasanain Hamid, Hussain-Alkhateeb, Laith, Farholt, Stense, Nørregaard, Ole, Jørgensen, Anders Palmstrøm, Hoybye, Charlotte
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Online Only Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8372636/
https://www.ncbi.nlm.nih.gov/pubmed/33950234
http://dx.doi.org/10.1210/clinem/dgab300

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8372636/
https://www.ncbi.nlm.nih.gov/pubmed/33950234
http://dx.doi.org/10.1210/clinem/dgab300

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