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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Detalles Bibliográficos
Autores principales: 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: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4855494/
https://www.ncbi.nlm.nih.gov/pubmed/27146407
http://dx.doi.org/10.1186/s13023-016-0440-0

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4855494/
https://www.ncbi.nlm.nih.gov/pubmed/27146407
http://dx.doi.org/10.1186/s13023-016-0440-0

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