ロード中...
Twenty Years of GH Treatment in Adults with Prader-Willi Syndrome
Prader-Willi syndrome (PWS) is a rare neurodevelopmental genetic disorder. In adults, the syndrome is characterised by muscular hypotonia, a different body composition with more body fat than muscle mass, hyperphagia, behavioural problems, and cognitive dysfunction. Endocrine deficiencies are common...
保存先:
| 出版年: | J Clin Med |
|---|---|
| 主要な著者: | , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
MDPI
2021
|
| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8234514/ https://ncbi.nlm.nih.gov/pubmed/34204309 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/jcm10122667 |
| タグ: |
タグ追加
タグなし, このレコードへの初めてのタグを付けませんか!
|