Literature DB >> 14595657

Functional neuroimaging provides evidence of anomalous cerebral laterality in adults with Klinefelter's syndrome.

Emmanuel Itti1, Irene T Gaw Gonzalo, Kyle B Boone, Daniel H Geschwind, Nancy Berman, Anna Pawlikowska-Haddal, Laurent Itti, Fred S Mishkin, Ronald S Swerdloff.   

Abstract

This study aimed to characterize cerebral perfusion in men with Klinefelter's syndrome, known to present specific deficits in language, using (99m)Tc- hexamethylpropylene-amine-oxime scintigraphy and Talairach normalization. While a perfusion asymmetry toward the left hemisphere was found in controls, perfusion was mostly symmetrical in Klinefelter patients in the upper temporal and lower parietal areas. Scores on verbal tests were inversely correlated with perfusion changes, providing neurobiological substrate of anomalous cerebral laterality.

Entities:  

Mesh:

Year:  2003        PMID: 14595657     DOI: 10.1002/ana.10735

Source DB:  PubMed          Journal:  Ann Neurol        ISSN: 0364-5134            Impact factor:   10.422


  8 in total

Review 1.  Structural and functional neuroimaging in Klinefelter (47,XXY) syndrome: a review of the literature and preliminary results from a functional magnetic resonance imaging study of language.

Authors:  Kyle Steinman; Judith Ross; Song Lai; Allan Reiss; Fumiko Hoeft
Journal:  Dev Disabil Res Rev       Date:  2009

Review 2.  Effects of sex chromosome aneuploidies on brain development: evidence from neuroimaging studies.

Authors:  Rhoshel K Lenroot; Nancy Raitano Lee; Jay N Giedd
Journal:  Dev Disabil Res Rev       Date:  2009

Review 3.  The cognitive phenotype in Klinefelter syndrome: a review of the literature including genetic and hormonal factors.

Authors:  Richard Boada; Jennifer Janusz; Christa Hutaff-Lee; Nicole Tartaglia
Journal:  Dev Disabil Res Rev       Date:  2009

Review 4.  Autism-lessons from the X chromosome.

Authors:  Elysa J Marco; David H Skuse
Journal:  Soc Cogn Affect Neurosci       Date:  2006-12       Impact factor: 3.436

5.  Protocadherin 11X/Y a human-specific gene pair: an immunohistochemical survey of fetal and adult brains.

Authors:  Thomas H Priddle; Tim J Crow
Journal:  Cereb Cortex       Date:  2012-06-28       Impact factor: 5.357

6.  Genomic sister-disorders of neurodevelopment: an evolutionary approach.

Authors:  Bernard Crespi; Kyle Summers; Steve Dorus
Journal:  Evol Appl       Date:  2009-01-07       Impact factor: 5.183

Review 7.  Genetic Consideration of Schizotypal Traits: A Review.

Authors:  Emma E Walter; Francesca Fernandez; Mollie Snelling; Emma Barkus
Journal:  Front Psychol       Date:  2016-11-15

8.  Sex chromosome trisomies are not associated with atypical lateralization for language.

Authors:  Alexander C Wilson; Dorothy V M Bishop
Journal:  Dev Med Child Neurol       Date:  2018-06-10       Impact factor: 5.449

  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.