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The Prader-Willi syndrome Profile: Validation of a new measures of behavioral and emotional problems in Prader-Willi syndrome

2023-06-22

Abstract excerpt

<h4>Background: </h4> 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 outbursts, aggressivity, and skin-picking. Questionnaires exist for measuring hyperphagia, but not for the aggrega...

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Literature Corpus work
05c80c83-ae91-5929-be9f-e8234eae0184
DOI
10.21203/rs.3.rs-3092957/v1
Open publication

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The Prader-Willi syndrome Profile: Validation of a new measures of behavioral and emotional problems in Prader-Willi syndromeDOI 10.21203/rs.3.rs-3092957/v1
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