An Adapted Model for Transition to Adult Care in Young Adults with Prader–Willi Syndrome
An Adapted Model for Transition to Adult Care in Young Adults with Prader–Willi Syndrome
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Basel: MDPI AG
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English
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Basel: MDPI AG
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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, and behavioral problems, appear or worsen in you...
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Full title
An Adapted Model for Transition to Adult Care in Young Adults with Prader–Willi Syndrome
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TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8124992
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https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8124992
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ISSN
2077-0383
E-ISSN
2077-0383
DOI
10.3390/jcm10091991