Endocrine manifestations and management of Prader-Willi syndrome

Prader-Willi syndrome (PWS) is a complex genetic disorder, caused by lack of expression of genes on the paternally inherited chromosome 15q11.2-q13. In infancy it is characterized by hypotonia with poor suck resulting in failure to thrive. As the child ages, other manifestations such as developmenta...

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Detalles Bibliográficos
Autores principales: Emerick, Jill E, Vogt, Karen S
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
PES Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3751775/
https://www.ncbi.nlm.nih.gov/pubmed/23962041
http://dx.doi.org/10.1186/1687-9856-2013-14

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3751775/
https://www.ncbi.nlm.nih.gov/pubmed/23962041
http://dx.doi.org/10.1186/1687-9856-2013-14

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