Twenty Years of GH Treatment in Adults with Prader-Willi Syndrome

Prader-Willi syndrome (PWS) is a rare neurodevelopmental genetic disorder. In adults, the syndrome is characterised by muscular hypotonia, a different body composition with more body fat than muscle mass, hyperphagia, behavioural problems, and cognitive dysfunction. Endocrine deficiencies are common...

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Detalles Bibliográficos
Autores principales: Sjöström, Anna, Höybye, Charlotte
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8234514/
https://www.ncbi.nlm.nih.gov/pubmed/34204309
http://dx.doi.org/10.3390/jcm10122667

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8234514/
https://www.ncbi.nlm.nih.gov/pubmed/34204309
http://dx.doi.org/10.3390/jcm10122667

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