The Prader-Willi syndrome Profile: validation of a new measure of behavioral and emotional problems in Prader-Willi syndrome
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 ...
Source: Orphanet Journal of Rare Diseases - Category: Internal Medicine Authors: Elisabeth M. Dykens, Elizabeth Roof and Hailee Hunt-Hawkins Tags: Research Source Type: research