Cargando...
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...
Guardado en:
| Publicado en: | Diseases |
|---|---|
| Autores principales: | , , |
| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
MDPI
2015
|
| Materias: | |
| Acceso en línea: | 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 |
| Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|