Mapping the evidence of multidimensional health approaches in treating individuals with Prader–Willi Syndrome: A scoping review protocol

INTRODUCTION: Prader–Willi Syndrome (PWS) is one of the rare diseases involving genetics and affects various body systems. The disease is known due to the absence of paternal genes on chromosome 15q11-q13. Multisystem complex conditions require interdisciplinary healthcare treatment. However, to the...

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Detalles Bibliográficos
Autores principales: Che Din, Normah, Umat, Cila, Abdul Wahat, Nor Haniza, Talib, Azhar Bin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2022
Materias:
Health Services Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8756288/
https://www.ncbi.nlm.nih.gov/pubmed/35022164
http://dx.doi.org/10.1136/bmjopen-2020-047638

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8756288/
https://www.ncbi.nlm.nih.gov/pubmed/35022164
http://dx.doi.org/10.1136/bmjopen-2020-047638

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