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Medication Trials for Hyperphagia and Food-Related Behaviors in Prader–Willi Syndrome
Prader-Willi syndrome (PWS) is a neurodevelopmental disorder caused by the absence of paternally expressed, imprinted genes on chromosome 15q11-13. Individuals with PWS characteristically have poor feeding and lack of appetite in infancy, followed by the development of weight gain and then uncontrol...
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| Publicado no: | Diseases |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
MDPI
2015
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5548239/ https://ncbi.nlm.nih.gov/pubmed/28943610 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/diseases3020078 |
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