Bone Health in Adults With Prader–Willi Syndrome: Clinical Recommendations Based on a Multicenter Cohort Study

CONTEXT: Prader–Willi syndrome (PWS) is a rare complex genetic syndrome, characterized by delayed psychomotor development, hypotonia, and hyperphagia. Hormone deficiencies such as hypogonadism, hypothyroidism, and growth hormone deficiency are common. The combination of hypotonia, low physical activ...

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Detalles Bibliográficos
Autores principales: van Abswoude, Denise H, Pellikaan, Karlijn, Rosenberg, Anna G W, Davidse, Kirsten, Coupaye, Muriel, Høybye, Charlotte, Markovic, Tania P, Grugni, Graziano, Crinò, Antonino, Caixàs, Assumpta, Poitou, Christine, Mosbah, Helena, Weir, Tessa, van Vlimmeren, Leo A, Rutges, Joost P H J, De Klerk, Luuk W L, Zillikens, M Carola, van der Lely, Aart J, de Graaff, Laura C G
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Clinical Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9759176/
https://www.ncbi.nlm.nih.gov/pubmed/36149817
http://dx.doi.org/10.1210/clinem/dgac556

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9759176/
https://www.ncbi.nlm.nih.gov/pubmed/36149817
http://dx.doi.org/10.1210/clinem/dgac556

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