%0 Journal Article
%T Behavioral phenotype in a child with Prader-Willi syndrome and comorbid 47, XYY.
%A Palkar P
%A Kabasakalian A
%A Taylor B
%A Doernberg E
%A Ferretti CJ
%A Uzunova G
%A Hollander E
%J Intractable Rare Dis Res
%V 5
%N 3
%D Aug 2016
%M 27672550
暂无%R 10.5582/irdr.2016.01043
%X We report a 12-year-old male with Prader-Willi syndrome (PWS) and 47, XYY syndrome. Genetic work up revealed 47, XYY karyotype. PWS diagnosis was made by polymerase chain reaction methylation and maternal uniparental disomy (mUPD) was determined to be the etiology. Review of distinct behavioral features, possible interplay between the two syndromes and considerations for diagnoses are presented. To our knowledge, this is the first report of behavioral features in PWS with comorbid 47, XYY.