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Quality of Life in Children with Prader–Willi Syndrome and the Impact of the Disease on the Functioning of Families
Objective: Prader–Willi (PWS; OMIM#176270) syndrome is a clinically distinct genetic disorder, caused by an abnormality in the 15q11-q13 region, referred to as the critical region. One of the most popular concepts existing in modern sciences, not only within psychology, but also in the aspect of all...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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MDPI
2022
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9740001/ https://www.ncbi.nlm.nih.gov/pubmed/36498413 http://dx.doi.org/10.3390/ijerph192316330 |