The Prader-Willi syndrome Profile: validation of a new measure of behavioral and emotional problems in Prader-Willi syndrome

Abstract Background Prader-Willi syndrome (PWS) is a rare, neurodevelopmental disorder caused by the lack of expression of paternally imprinted genes on chromosome 15q11-13. PWS features a complex behavioral phenotype, including hyperphagia, anxiety, compulsivity, rigidity, repetitive speech, temper...

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Autori principali:	Elisabeth M. Dykens, Elizabeth Roof, Hailee Hunt-Hawkins
Natura:	Artigo
Lingua:	Inglês
Pubblicazione:	BMC 2024-02-01
Serie:	Orphanet Journal of Rare Diseases
Soggetti:	PWS Profile Behavioral and emotional dysfunction in PWS Anxiety Clinical trials Endpoints
Accesso online:	https://doi.org/10.1186/s13023-024-03045-9
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