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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Bibliographic Details
Main Authors: Anna Sjöström, Karlijn Pellikaan, Henrik Sjöström, Anthony P. Goldstone, Graziano Grugni, Antonino Crinò, Laura C. G. De Graaff, Charlotte Höybye
Format: Article
Language:English
Published: MDPI AG 2021-08-01
Series:Journal of Clinical Medicine
Subjects:
Online Access:https://www.mdpi.com/2077-0383/10/16/3613