Review of Prader-Willi syndrome: the endocrine approach

Prader-Willi syndrome (PWS) is a complex genetic disorder with implications on the endocrine and neurologic systems, metabolism, and behavior. Early in life, PWS is characterized by hypotonia and failure to thrive, followed by obesity and hyperphagia. Patients with PWS develop hypothalamic dysfuncti...

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Bibliografiske detaljer
Udgivet i:Transl Pediatr
Main Authors: Heksch, Ryan, Kamboj, Manmohan, Anglin, Kathryn, Obrynba, Kathryn
Format: Artigo
Sprog:Inglês
Udgivet: AME Publishing Company 2017
Fag:
Review Article
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC5682385/
https://ncbi.nlm.nih.gov/pubmed/29184809
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.21037/tp.2017.09.04
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