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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

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