RF17 | PMON27 Genetic Subtype Differences in Relation to Health Problems Among Adults With Prader-Willi Syndrome

BACKGROUND: Prader-Willi syndrome (PWS) is a complex rare genetic disorder associated with hypothalamic dysfunction, pituitary hormone deficiencies, hyperphagia and (morbid) obesity. PWS is caused by loss of expression of paternally expressed genes on chromosome 15q11.2-q13. The most common genetic...

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Detalles Bibliográficos
Autores principales: Pellikaan, Karlijn, Rosenberg, Anna, Wellink, Charlotte, Garcia, Juan Tellez, van Abswoude, Denise, van Zutven, Laura, Brüggenwirth, Hennie, Resnick, James, van der Lely, Aart Jan, de Graaff, Laura
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Genetics & Development
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9625281/
http://dx.doi.org/10.1210/jendso/bvac150.964

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9625281/
http://dx.doi.org/10.1210/jendso/bvac150.964

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