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- W2002133797 abstract "Prader-Willi Syndrome (PWS) is a complex multisystem genetic disorder that shows great variability, with changing clinical features during a patient’s life. The syndrome is due to the loss of expression of several genes encoded on the proximal long arm of chromosome 15 (15q11.2–q13). The complex phenotype is most probably caused by a hypothalamic dysfunction that is responsible for hormonal dysfunctions and for absence of the sense of satiety. For this reason a Prader-Willi (PW) child develops hyperphagia during the initial stage of infancy that can lead to obesity and its complications. During infancy many PW child display a range of behavioural problems that become more noticeable in adolescence and adulthood and interfere mostly with quality of life. Early diagnosis of PWS is important for effective long-term management, and a precocious multidisciplinary approach is fundamental to improve quality of life, prevent complications, and prolong life expectancy." @default.
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- W2002133797 date "2012-01-01" @default.
- W2002133797 modified "2023-10-11" @default.
- W2002133797 title "Prader-Willi Syndrome: Clinical Aspects" @default.
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- W2002133797 doi "https://doi.org/10.1155/2012/473941" @default.
- W2002133797 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/3486015" @default.
- W2002133797 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/23133744" @default.
- W2002133797 hasPublicationYear "2012" @default.
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