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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...

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Detalhes bibliográficos
Publicado no:Int J Mol Sci
Main Authors: Noordam, Cees, Höybye, Charlotte, Eiholzer, Urs
Formato: Artigo
Idioma:Inglês
Publicado em: MDPI 2021
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7962179/
https://ncbi.nlm.nih.gov/pubmed/33800122
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/ijms22052705
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