Prader–Willi Syndrome and Hypogonadism: A Review Article

Prader–Willi Syndrome and Hypogonadism: A Review Article

Prader-Labhart-Willi syndrome (PWS) is a rare genetic disorder characterized by intellectual disability, behavioural problems, hypothalamic dysfunction and specific dysmorphisms. Hypothalamic dysfunction causes dysregulation of energy balance and endocrine deficiencies, including hypogonadism. Altho...

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Bibliographic Details
Main Authors: Cees Noordam, Charlotte Höybye, Urs Eiholzer
Format: Article
Language:English
Published: MDPI AG 2021-03-01
Series:International Journal of Molecular Sciences
Subjects:
Prader-Willi syndrome
hypogonadism
child
adult
review
diagnosis
Online Access:https://www.mdpi.com/1422-0067/22/5/2705

Internet

https://www.mdpi.com/1422-0067/22/5/2705

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