Hyperprolactinemia in Adults with Prader-Willi Syndrome

Prader-Willi syndrome (PWS) is a rare neurodevelopmental genetic disorder typically characterized by body composition abnormalities, hyperphagia, behavioural challenges, cognitive dysfunction, and hypogonadism. Psychotic illness is common, particularly in patients with maternal uniparental disomy (m...

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Detalles Bibliográficos
Autores principales: Sjöström, Anna, Pellikaan, Karlijn, Sjöström, Henrik, Goldstone, Anthony P., Grugni, Graziano, Crinò, Antonino, De Graaff, Laura C. G., Höybye, Charlotte
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8396901/
https://www.ncbi.nlm.nih.gov/pubmed/34441908
http://dx.doi.org/10.3390/jcm10163613

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8396901/
https://www.ncbi.nlm.nih.gov/pubmed/34441908
http://dx.doi.org/10.3390/jcm10163613

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