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Clinical Observations and Treatment Approaches for Scoliosis in Prader–Willi Syndrome
Prader–Willi syndrome (PWS) is recognized as the first example of genomic imprinting, generally due to a de novo paternal 15q11-q13 deletion. PWS is considered the most common genetic cause of marked obesity in humans. Scoliosis, kyphosis, and kyphoscoliosis are commonly seen in children and adolesc...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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MDPI
2020
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7140837/ https://www.ncbi.nlm.nih.gov/pubmed/32121146 http://dx.doi.org/10.3390/genes11030260 |