High unacylated ghrelin levels support the concept of anorexia in infants with prader-willi syndrome

BACKGROUND: Prader-Willi syndrome (PWS) is a rare genetic neurodevelopmental disorder with different nutritional phases from suckling deficit with failure to thrive to early onset of obesity. Hyperghrelinemia has been described in PWS long before the development of obesity. Ghrelin is found in both...

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Detalhes bibliográficos
Publicado no:Orphanet J Rare Dis
Main Authors: Beauloye, Veronique, Diene, Gwenaelle, Kuppens, Renske, Zech, Francis, Winandy, Coralie, Molinas, Catherine, Faye, Sandy, Kieffer, Isabelle, Beckers, Dominique, Nergårdh, Ricard, Hauffa, Berthold, Derycke, Christine, Delhanty, Patrick, Hokken-Koelega, Anita, Tauber, Maithé
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2016
Assuntos:
Research
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4855494/
https://ncbi.nlm.nih.gov/pubmed/27146407
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13023-016-0440-0
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