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Systematic review of the clinical and genetic aspects of Prader-Willi syndrome
Prader-Willi syndrome (PWS) is a complex multisystem genetic disorder that is caused by the lack of expression of paternally inherited imprinted genes on chromosome 15q11-q13. This syndrome has a characteristic phenotype including severe neonatal hypotonia, early-onset hyperphagia, development of mo...
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| Formato: | Texto |
| Lenguaje: | English |
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The Korean Pediatric Society
2011
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3077502/ https://www.ncbi.nlm.nih.gov/pubmed/21503198 http://dx.doi.org/10.3345/kjp.2011.54.2.55 |