Approach to the Patient With Prader–Willi Syndrome

Prader–Willi syndrome (PWS) is a rare, multisystemic, genetic disorder involving the hypothalamus. It is caused by loss of expression of paternally inherited genes in chromosome 15 q11-13 region. The estimated incidence is around 1 in 20.000 births. PWS is characterized by a complex lifelong traject...

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Detalles Bibliográficos
Autores principales: Höybye, Charlotte, Tauber, Maithé
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Approach to the Patient
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9635059/
https://www.ncbi.nlm.nih.gov/pubmed/35150573
http://dx.doi.org/10.1210/clinem/dgac082

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9635059/
https://www.ncbi.nlm.nih.gov/pubmed/35150573
http://dx.doi.org/10.1210/clinem/dgac082

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