High levels of caregiver burden in Prader-Willi syndrome

OBJECTIVES: Prader-Willi syndrome (PWS) is a rare genetic neurodevelopmental disorder that is characterized by hyperphagia, developmental delay, incomplete sexual development, mild-to-moderate intellectual disability, and a variety of challenging behavioral and psychiatric symptoms. The characterist...

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Detalles Bibliográficos
Autores principales: Kayadjanian, Nathalie, Schwartz, Lauren, Farrar, Evan, Comtois, Katherine Anne, Strong, Theresa V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5868812/
https://www.ncbi.nlm.nih.gov/pubmed/29579119
http://dx.doi.org/10.1371/journal.pone.0194655

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5868812/
https://www.ncbi.nlm.nih.gov/pubmed/29579119
http://dx.doi.org/10.1371/journal.pone.0194655

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