SAGE Reference - Encyclopedia of Global Health

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Prader-Willi Syndrome

By: Sarah Boslaugh
In: Encyclopedia of Global Health
Edited by: Yawei Zhang
Subject:Public Health (general), Public Health Education & Health Promotion

Prader-Willi syndrome (PWS) is a rare, inherited chromosomal disorder arising from deletion or disruption of genes in the proximal arm of chromosome 15. It was first described in 1956 by Andrea Prader, Heinrich Willi, Alexis Labhart, Andrew Ziegler, and Guido Fanconi ...

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  Boslaugh, S. (2008). Prader-willi syndrome. In Y. Zhang (Ed.), Encyclopedia of global health (Vol. 1, pp. 1409-1409). SAGE Publications, Inc., https://www.doi.org/10.4135/9781412963855.n994
  
  Boslaugh, Sarah. "Prader-Willi Syndrome." In Encyclopedia of Global Health, edited by Zhang, Yawei, 1409-1409. Thousand Oaks, CA: SAGE Publications, Inc., 2008. http://dx.doi.org/10.4135/9781412963855.n994.
  
  Boslaugh, S. 2008. Prader-Willi Syndrome. In: Yawei Zhang Editor, 2008. Encyclopedia of Global Health, Thousand Oaks, CA: SAGE Publications, Inc. pp. 1409 Available at: <http://www.doi.org/10.4135/9781412963855.n994> [Accessed 22 Apr 2021].
  
  Boslaugh, Sarah. "Prader-Willi Syndrome." Encyclopedia of Global Health. Edited by Yawei Zhang. Vol. 1. Thousand Oaks: SAGE Publications, Inc., 2008, pp. 1409-1409. SAGE Knowledge. 22 Apr 2021, doi: http://www.doi.org/10.4135/9781412963855.n994.
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