| Literature DB >> 32468713 |
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.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