Recommendations for the diagnosis and management of childhood Prader-Willi syndrome in China

Prader-Willi syndrome (PWS) is a complex and multisystem neurobehavioral disease, which is caused by the lack of expression of paternally inherited imprinted genes on chromosome15q11.2-q13.1. The clinical manifestations of PWS vary with age. It is characterized by severe hypotonia with poor suck and...

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Detalles Bibliográficos
Autores principales: Yang-Li, Dai, Fei-Hong, Luo, Hui-Wen, Zhang, Ming-Sheng, Ma, Xiao-Ping, Luo, Li, Liu, Yi, Wang, Qing, Zhou, Yong-Hui, Jiang, Chao-Chun, Zou
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9195308/
https://www.ncbi.nlm.nih.gov/pubmed/35698200
http://dx.doi.org/10.1186/s13023-022-02302-z

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9195308/
https://www.ncbi.nlm.nih.gov/pubmed/35698200
http://dx.doi.org/10.1186/s13023-022-02302-z

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