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...

Descripción completa

Detalles Bibliográficos
Autores principales: Noordam, Cees, Höybye, Charlotte, Eiholzer, Urs
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Review
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

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7962179/
https://www.ncbi.nlm.nih.gov/pubmed/33800122
http://dx.doi.org/10.3390/ijms22052705

Ejemplares similares