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Time for a general approval of growth hormone treatment in adults with Prader–Willi syndrome
Prader-Willi syndrome (PWS) is a complex, multi-system, neurodevelopmental disorder characterised by neonatal muscular hypotonia, short stature, high risk of obesity, hypogonadism, intellectual disabilities, distinct behavioural/psychiatric problems and abnormal body composition with increased body...
保存先:
| 出版年: | Orphanet J Rare Dis |
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| 主要な著者: | , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
BioMed Central
2021
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7869190/ https://ncbi.nlm.nih.gov/pubmed/33557878 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13023-020-01651-x |
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