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Prader–Willi Syndrome in Adults: An Update On Nutritional Treatment and Pharmacological Approach

PURPOSE OF REVIEW: Prader–Willi syndrome (PWS) is a rare and complex genetic disorder with multiple effects on the metabolic, endocrine, and neurological systems, as well as behavioral and intellectual difficulties. Despite advances in understanding the genetic basis of obesity in PWS, there are con...

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Detalles Bibliográficos
Autores principales: Barrea, Luigi, Vetrani, Claudia, Fintini, Danilo, de Alteriis, Giulia, Panfili, Filippo Maria, Bocchini, Sarah, Verde, Ludovica, Colao, Annamaria, Savastano, Silvia, Muscogiuri, Giovanna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9729321/
https://www.ncbi.nlm.nih.gov/pubmed/36063285
http://dx.doi.org/10.1007/s13679-022-00478-w

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