Obesity management in Prader–Willi syndrome: current perspectives

Prader–Willi syndrome (PWS) is a complex multisystem disorder due to the absent expression of the paternally active genes in the PWS critical region on chromosome 15 (15q11.2-q13). The syndrome is considered the most common genetic cause of obesity, occurring in 1:10,000–1:30,000 live births. Its ma...

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Detalles Bibliográficos
Autores principales: Crinò, Antonino, Fintini, Danilo, Bocchini, Sarah, Grugni, Graziano
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2018
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6175547/
https://www.ncbi.nlm.nih.gov/pubmed/30323638
http://dx.doi.org/10.2147/DMSO.S141352

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6175547/
https://www.ncbi.nlm.nih.gov/pubmed/30323638
http://dx.doi.org/10.2147/DMSO.S141352

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