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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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| 主要な著者: | , |
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| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Galenos Publishing
2014
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| 主題: | |
| オンライン･アクセス: | 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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