Hypogonadism in Women with Prader-Willi Syndrome—Clinical Recommendations Based on a Dutch Cohort Study, Review of the Literature and an International Expert Panel Discussion

Prader-Willi syndrome (PWS) is a rare neuroendocrine genetic syndrome. Characteristics of PWS include hyperphagia, hypotonia, and intellectual disability. Pituitary hormone deficiencies, caused by hypothalamic dysfunction, are common and hypogonadism is the most prevalent. Untreated hypogonadism can...

Descripción completa

Detalles Bibliográficos
Autores principales: Pellikaan, Karlijn, Ben Brahim, Yassine, Rosenberg, Anna G. W., Davidse, Kirsten, Poitou, Christine, Coupaye, Muriel, Goldstone, Anthony P., Høybye, Charlotte, Markovic, Tania P., Grugni, Graziano, Crinò, Antonino, Caixàs, Assumpta, Eldar-Geva, Talia, Hirsch, Harry J., Gross-Tsur, Varda, Butler, Merlin G., Miller, Jennifer L., van der Kuy, Paul-Hugo M., van den Berg, Sjoerd A. A., Visser, Jenny A., van der Lely, Aart J., de Graaff, Laura C. G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8707541/
https://www.ncbi.nlm.nih.gov/pubmed/34945077
http://dx.doi.org/10.3390/jcm10245781

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8707541/
https://www.ncbi.nlm.nih.gov/pubmed/34945077
http://dx.doi.org/10.3390/jcm10245781

Ejemplares similares