White matter microstructural abnormalities in girls with chromosome 22q11.2 deletion syndrome, Fragile X or Turner syndrome as evidenced by diffusion tensor imaging

@article{Villalon2013WhiteMM,
  title={White matter microstructural abnormalities in girls with chromosome 22q11.2 deletion syndrome, Fragile X or Turner syndrome as evidenced by diffusion tensor imaging},
  author={Julio Villalon and Neda Jahanshad and Elliott A Beaton and Arthur W. Toga and Paul M. Thompson and Tony J. Simon},
  journal={NeuroImage},
  year={2013},
  volume={81},
  pages={
          441-454
        }
}
Children with chromosome 22q11.2 deletion syndrome (22q11.2DS), Fragile X syndrome (FXS), or Turner syndrome (TS) are considered to belong to distinct genetic groups, as each disorder is caused by separate genetic alterations. Even so, they have similar cognitive and behavioral dysfunctions, particularly in visuospatial and numerical abilities. To assess evidence for common underlying neural microstructural alterations, we set out to determine whether these groups have partially overlapping… CONTINUE READING
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