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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...
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| Foilsithe in: | J Clin Med |
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| Main Authors: | , |
| Formáid: | Artigo |
| Teanga: | Inglês |
| Foilsithe: |
MDPI
2021
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| Ábhair: | |
| Rochtain Ar Líne: | 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 |
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