Kidney disease in adults with Prader-Willi syndrome: international cohort study and systematic literature review

BACKGROUND: Prader-Willi syndrome (PWS) is a rare, complex, genetic disorder characterized by hyperphagia, hypotonia, delayed psychomotor development, low muscle mass and hypothalamic dysfunction. Adults with PWS often have obesity, hypertension and type 2 diabetes mellitus (DM2), known risk factors...

Descripción completa

Detalles Bibliográficos
Autores principales: van Abswoude, Denise H., Pellikaan, Karlijn, Nguyen, Naomi, Rosenberg, Anna G. W., Davidse, Kirsten, Hoekstra, Franciska M. E., Rood, Ilse M., Poitou, Christine, Grugni, Graziano, Høybye, Charlotte, Markovic, Tania P., Caixàs, Assumpta, Crinò, Antonino, van den Berg, Sjoerd A. A., van der Lely, Aart J., de Graaff, Laura C. G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Endocrinology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10402738/
https://www.ncbi.nlm.nih.gov/pubmed/37547314
http://dx.doi.org/10.3389/fendo.2023.1168648

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10402738/
https://www.ncbi.nlm.nih.gov/pubmed/37547314
http://dx.doi.org/10.3389/fendo.2023.1168648

Ejemplares similares