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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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| Publicat a: | Transl Pediatr |
|---|---|
| Autors principals: | , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
AME Publishing Company
2017
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| Matèries: | |
| Accés en línia: | 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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