Prader–Willi syndrome in neonates: twenty cases and review of the literature in Southern China

BACKGROUND: Prader-Willi syndrome is a rare genetic abnormality that can be challenging to diagnose early, but for which early interventions improve prognosis. METHODS: To improve understanding of Prader–Willi syndrome in neonates in Asia, we retrospectively analyzed the clinical records of 20 affec...

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Detalles Bibliográficos
Autores principales: Wang, Ping, Zhou, Wei, Yuan, Weiming, Huang, Longguang, Zhao, Ning, Chen, Xiaowen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4977863/
https://www.ncbi.nlm.nih.gov/pubmed/27506196
http://dx.doi.org/10.1186/s12887-016-0662-2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4977863/
https://www.ncbi.nlm.nih.gov/pubmed/27506196
http://dx.doi.org/10.1186/s12887-016-0662-2

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