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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...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: Emerick, Jill E, Vogt, Karen S
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: BioMed Central 2013
Gaiak:
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC3751775/
https://ncbi.nlm.nih.gov/pubmed/23962041
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1687-9856-2013-14
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