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French database of children and adolescents with Prader-Willi syndrome

BACKGROUND: Prader-Willi syndrome (PWS) is a rare multisystem genetic disease leading to severe complications mainly related to obesity. We strongly lack information on the natural history of this complex disease and on what factors are involved in its evolution and its outcome. One of the objective...

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Autori principali: Molinas, Catherine, Cazals, Laurent, Diene, Gwenaelle, Glattard, Melanie, Arnaud, Catherine, Tauber, Maithe
Natura: Artigo
Lingua:Inglês
Pubblicazione: BioMed Central 2008
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Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC2569911/
https://ncbi.nlm.nih.gov/pubmed/18831731
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2350-9-89
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