An Adapted Model for Transition to Adult Care in Young Adults with Prader–Willi Syndrome

Background: Prader–Willi syndrome (PWS) is a rare, neurodevelopmental, genetic disease caused by the lack of expression of paternal genes in chromosome 15. The typical characteristics, including hyperphagia, muscular hypotonia, abnormal body composition, hormonal deficiencies, cognitive disabilities...

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Detalles Bibliográficos
Autores principales: Pedersen, Maria, Höybye, Charlotte
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8124992/
https://www.ncbi.nlm.nih.gov/pubmed/34066432
http://dx.doi.org/10.3390/jcm10091991

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8124992/
https://www.ncbi.nlm.nih.gov/pubmed/34066432
http://dx.doi.org/10.3390/jcm10091991

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