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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Vydáno v:Orphanet J Rare Dis
Hlavní autoři: 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
Médium: Artigo
Jazyk:Inglês
Vydáno: BioMed Central 2016
Témata:
Research
On-line přístup: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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