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...

תיאור מלא

שמור ב:
מידע ביבליוגרפי
הוצא לאור ב: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
פורמט: Artigo
שפה:Inglês
יצא לאור: BioMed Central 2016
נושאים:
Research
גישה מקוונת: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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