Obesity in Prader–Willi syndrome: physiopathological mechanisms, nutritional and pharmacological approaches

Prader–Willi syndrome (PWS) is a genetic disorder caused by the lack of expression of genes on the paternally inherited chromosome 15q11.2-q13 region. The three main genetic subtypes are represented by paternal 15q11-q13 deletion, maternal uniparental disomy 15, and imprinting defect. Clinical pictu...

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Detalles Bibliográficos
Autores principales: Muscogiuri, G., Barrea, L., Faggiano, F., Maiorino, M. I., Parrillo, M., Pugliese, G., Ruggeri, R. M., Scarano, E., Savastano, S., Colao, A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2021
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8421305/
https://www.ncbi.nlm.nih.gov/pubmed/33891302
http://dx.doi.org/10.1007/s40618-021-01574-9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8421305/
https://www.ncbi.nlm.nih.gov/pubmed/33891302
http://dx.doi.org/10.1007/s40618-021-01574-9

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