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An Adapted Model for Transition to Adult Care in Young Adults with Prader–Willi Syndrome
Background: Prader–Willi syndrome (PWS) is a rare, neurodevelopmental, genetic disease caused by the lack of expression of paternal genes in chromosome 15. The typical characteristics, including hyperphagia, muscular hypotonia, abnormal body composition, hormonal deficiencies, cognitive disabilities...
Uloženo v:
| Vydáno v: | J Clin Med |
|---|---|
| Hlavní autoři: | , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
MDPI
2021
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8124992/ https://ncbi.nlm.nih.gov/pubmed/34066432 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/jcm10091991 |
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