Literature DB >> 29406610

The nature of social cognitive deficits in children and adults with Klinefelter syndrome (47,XXY).

S van Rijn1,2, L de Sonneville1,2, H Swaab1,2.   

Abstract

About 1 in 650 boys are born with an extra X chromosome (47,XXY or Klinefelter syndrome). 47,XXY is associated with vulnerabilities in socio-emotional development. This study was designed to assess types of cognitive deficits in individuals with 47,XXY that may contribute to social-emotional dysfunction, and to evaluate the nature of such deficits at various levels: ranging from basic visuospatial processing deficits, impairments in face recognition (FR), to emotion expression impairments. A total of 70 boys and men with 47,XXY, aged 8 to 60 years old, participated in the study. The subtests feature identification, FR and identification of facial emotions of the Amsterdam Neuropsychological Tasks were used. Level of intellectual functioning was assessed with the child and adult versions of the Wechsler Intelligence Scales. Reaction time data showed that in the 47,XXY group, 17% had difficulties in visuospatial processing (no social load), 26% had difficulties with FR (medium social load) and an even higher number of 33% had difficulties with facial expressions of emotions (high-social load). Information processing impairments increased as a function of "social load" of the stimuli, independent of intellectual functioning. Taken together, our data suggest that on average individuals with XXY may have more difficulties in information processing when "social load" increases, suggesting a specific difficulty in the higher-order labeling and interpretation of social cues, which cannot be explained by more basic visuospatial perceptual skills. Considering the increased risk for social cognitive impairments, routine assessment of social cognitive functioning as part of neuropsychological screening is warranted.
© 2018 John Wiley & Sons Ltd and International Behavioural and Neural Genetics Society.

Entities:  

Keywords:  Klinefelter syndrome; X chromosome; XXY; cognition; emotions; facial expressions; sex chromosome aneuploidies; sex chromosome variations; social cognition; visual processing

Mesh:

Year:  2018        PMID: 29406610     DOI: 10.1111/gbb.12465

Source DB:  PubMed          Journal:  Genes Brain Behav        ISSN: 1601-183X            Impact factor:   3.449


  8 in total

Review 1.  A review of neurocognitive functioning and risk for psychopathology in sex chromosome trisomy (47,XXY, 47,XXX, 47, XYY).

Authors:  Sophie van Rijn
Journal:  Curr Opin Psychiatry       Date:  2019-03       Impact factor: 4.741

Review 2.  Early neurodevelopmental and medical profile in children with sex chromosome trisomies: Background for the prospective eXtraordinarY babies study to identify early risk factors and targets for intervention.

Authors:  Nicole Tartaglia; Susan Howell; Shanlee Davis; Karen Kowal; Tanea Tanda; Mariah Brown; Cristina Boada; Amanda Alston; Leah Crawford; Talia Thompson; Sophie van Rijn; Rebecca Wilson; Jennifer Janusz; Judith Ross
Journal:  Am J Med Genet C Semin Med Genet       Date:  2020-06-07       Impact factor: 3.908

3.  Educational status, testosterone replacement, and intelligence outcomes in Klinefelter syndrome.

Authors:  Luciane Simonetti; Magnus Regios Dias da Silva; Claudia Berlim de Mello
Journal:  Dement Neuropsychol       Date:  2022 Jan-Mar

4.  Cortical gray matter structure in boys with Klinefelter syndrome.

Authors:  Lara C Foland-Ross; Maureen Gil; Sharon Bade Shrestha; Lindsay C Chromik; David Hong; Allan L Reiss
Journal:  Psychiatry Res Neuroimaging       Date:  2021-05-04       Impact factor: 2.493

5.  A large data resource of genomic copy number variation across neurodevelopmental disorders.

Authors:  Mehdi Zarrei; Christie L Burton; Worrawat Engchuan; Edwin J Young; Edward J Higginbotham; Jeffrey R MacDonald; Brett Trost; Ada J S Chan; Susan Walker; Sylvia Lamoureux; Tracy Heung; Bahareh A Mojarad; Barbara Kellam; Tara Paton; Muhammad Faheem; Karin Miron; Chao Lu; Ting Wang; Kozue Samler; Xiaolin Wang; Gregory Costain; Ny Hoang; Giovanna Pellecchia; John Wei; Rohan V Patel; Bhooma Thiruvahindrapuram; Maian Roifman; Daniele Merico; Tara Goodale; Irene Drmic; Marsha Speevak; Jennifer L Howe; Ryan K C Yuen; Janet A Buchanan; Jacob A S Vorstman; Christian R Marshall; Richard F Wintle; David R Rosenberg; Gregory L Hanna; Marc Woodbury-Smith; Cheryl Cytrynbaum; Lonnie Zwaigenbaum; Mayada Elsabbagh; Janine Flanagan; Bridget A Fernandez; Melissa T Carter; Peter Szatmari; Wendy Roberts; Jason Lerch; Xudong Liu; Rob Nicolson; Stelios Georgiades; Rosanna Weksberg; Paul D Arnold; Anne S Bassett; Jennifer Crosbie; Russell Schachar; Dimitri J Stavropoulos; Evdokia Anagnostou; Stephen W Scherer
Journal:  NPJ Genom Med       Date:  2019-10-07       Impact factor: 8.617

Review 6.  A review of neurocognitive functioning of children with sex chromosome trisomies: Identifying targets for early intervention.

Authors:  Evelien Urbanus; Sophie van Rijn; Hanna Swaab
Journal:  Clin Genet       Date:  2019-07-11       Impact factor: 4.438

7.  Klinefelter syndrome mosaicism in boys with neurodevelopmental disorders: a cohort study and an extension of the hypothesis.

Authors:  Svetlana G Vorsanova; Irina A Demidova; Alexey D Kolotii; Oksana S Kurinnaia; Victor S Kravets; Ilya V Soloviev; Yuri B Yurov; Ivan Y Iourov
Journal:  Mol Cytogenet       Date:  2022-03-05       Impact factor: 2.009

8.  The impact of sex chromosome trisomies (XXX, XXY, XYY) on gaze towards faces and affect recognition: a cross-sectional eye tracking study.

Authors:  Nienke Bouw; Hanna Swaab; Nicole Tartaglia; Lisa Cordeiro; Sophie van Rijn
Journal:  J Neurodev Disord       Date:  2022-08-02       Impact factor: 4.074

  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.