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Prader-Willi Syndrome and Growth Hormone Deficiency
Prader-Willi syndrome (PWS) is a rare multisystem genetic disorder demonstrating great variability with changing clinical features during patient’s life. It is characterized by severe hypotonia with poor sucking and feeding difficulties in early infancy, followed by excessive eating and gradual deve...
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| Autors principals: | , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Galenos Publishing
2014
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4141577/ https://ncbi.nlm.nih.gov/pubmed/24932597 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4274/jcrpe.1228 |
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