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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...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
BMJ Publishing Group
2022
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| Materias: | |
| 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 |