Literature DB >> 32468713

Psychological functioning, brain morphology, and functional neuroimaging in Klinefelter syndrome.

Anne Skakkebaek1,2, Claus H Gravholt2,3, Simon Chang2,4, Philip J Moore5, Mikkel Wallentin6,7.   

Abstract

Klinefelter syndrome (KS; 47,XXY) impacts neurodevelopment and is associated with an increased risk of cognitive, psychological and social impairments, although significant heterogeneity in the neurodevelopmental profile is seen. KS is characterized by a specific cognitive profile with predominantly verbal deficits, preserved function in non-verbal and visuo-spatial domains, executive dysfunction and social impairments, and by an increased vulnerability toward psychiatric disorders. The neurobiological underpinnings of the observed neuropsychological profile have not been established. A distinct pattern of both global and regional brain volumetric differences has been demonstrated in addition to preliminary findings of functional brain alterations related to auditory, motor, language and social processing. When present, the combination of cognitive, psychological and social challenges has the potential to negatively affect quality of life. This review intends to provide information and insight to the neuropsychological outcome and brain correlates of KS. Possible clinical intervention and future directions of research will be discussed.
© 2020 Wiley Periodicals, Inc.

Entities:  

Keywords:  Klinefelter syndrome; brain morphology; cognition; neuropsychology; sex chromosomes

Mesh:

Year:  2020        PMID: 32468713     DOI: 10.1002/ajmg.c.31806

Source DB:  PubMed          Journal:  Am J Med Genet C Semin Med Genet        ISSN: 1552-4868            Impact factor:   3.908


  3 in total

1.  Sex chromosome aneuploidies in 2020-The state of care and research in the world.

Authors:  Claus H Gravholt; Nicole Tartaglia; Christine Disteche
Journal:  Am J Med Genet C Semin Med Genet       Date:  2020-06-04       Impact factor: 3.908

2.  A Patient with Moderate Intellectual Disability and 49, XXXYY Karyotype.

Authors:  Willem M A Verhoeven; Jos I M Egger; Sandra Mergler; Ton A A Meijer; Rolph Pfundt; Marjolein H Willemsen
Journal:  Int J Gen Med       Date:  2022-03-10

3.  Polymerase chain reaction-based assays facilitate the breeding and study of mouse models of Klinefelter syndrome.

Authors:  Hai-Xia Zhang; Yu-Lin Zhou; Wen-Yan Xu; Xiao-Lu Chen; Jia-Yang Jiang; Xiao-Man Zhou; Zeng-Ge Wang; Rong-Qin Ke; Qi-Wei Guo
Journal:  Asian J Androl       Date:  2022 Jan-Feb       Impact factor: 3.285

  3 in total

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