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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...
Autores principales: | Noordam, Cees, Höybye, Charlotte, Eiholzer, Urs |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7962179/ https://www.ncbi.nlm.nih.gov/pubmed/33800122 http://dx.doi.org/10.3390/ijms22052705 |
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