Dataset Information

Visuospatial interpolation in typically developing children and in people with Williams Syndrome.

ABSTRACT: Visuospatial interpolation is the estimation of object position or contour shape computed from known "anchor" positions. We characterized the developmental profile of interpolation by measuring positional thresholds as a function of inter-element separation without (Experiment 1) and with (Experiment 2) the context of illusory contours in typically developing children, typical adults and individuals with Williams Syndrome (WS), a genetic disorder that causes impaired global visuospatial abilities. We found that typically developing children and WS individuals had more difficulty integrating information across distant elements than typical adults. However, illusory contours improved thresholds in all participant groups in a similar way. Our results suggest that in WS individuals, and in typically developing children, the grouping mechanisms that enable long-range spatial integration are immature. We hypothesize that WS individuals and young children can use stimulus-driven grouping cues for bottom-up integration, but have immature mechanisms for top-down integration of spatial information.

SUBMITTER: Palomares M

PROVIDER: S-EPMC2577723 | biostudies-literature | 2008 Oct

REPOSITORIES: biostudies-literature

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Visuospatial interpolation in typically developing children and in people with Williams Syndrome.

Palomares Melanie M Landau Barbara B Egeth Howard H

Vision research 20080927 23-24

Visuospatial interpolation is the estimation of object position or contour shape computed from known "anchor" positions. We characterized the developmental profile of interpolation by measuring positional thresholds as a function of inter-element separation without (Experiment 1) and with (Experiment 2) the context of illusory contours in typically developing children, typical adults and individuals with Williams Syndrome (WS), a genetic disorder that causes impaired global visuospatial abilitie ...[more]

PMID: 18782587

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Project description:The emergence of resting-state functional connectivity (rsFC) analysis, which examines temporal correlations of low-frequency (<0.1 Hz) blood oxygen level-dependent signal fluctuations between brain regions, has dramatically improved our understanding of the functional architecture of the typically developing (TD) human brain. This study examined rsFC in Down syndrome (DS) compared with another neurodevelopmental disorder, Williams syndrome (WS), and TD. Ten subjects with DS, 18 subjects with WS, and 40 subjects with TD each participated in a 3-Tesla MRI scan. We tested for group differences (DS vs. TD, DS vs. WS, and WS vs. TD) in between- and within-network rsFC connectivity for seven functional networks. For the DS group, we also examined associations between rsFC and other cognitive and genetic risk factors. In DS compared with TD, we observed higher levels of between-network connectivity in 6 out 21 network pairs but no differences in within-network connectivity. Participants with WS showed lower levels of within-network connectivity and no significant differences in between-network connectivity relative to DS. Finally, our comparison between WS and TD controls revealed lower within-network connectivity in multiple networks and higher between-network connectivity in one network pair relative to TD controls. While preliminary due to modest sample sizes, our findings suggest a global difference in between-network connectivity in individuals with neurodevelopmental disorders compared with controls and that such a difference is exacerbated across many brain regions in DS. However, this alteration in DS does not appear to extend to within-network connections, and therefore, the altered between-network connectivity must be interpreted within the framework of an intact intra-network pattern of activity. In contrast, WS shows markedly lower levels of within-network connectivity in the default mode network and somatomotor network relative to controls. These findings warrant further investigation using a task-based procedure that may help disentangle the relationship between brain function and cognitive performance across the spectrum of neurodevelopmental disorders.

Dataset Information

Visuospatial interpolation in typically developing children and in people with Williams Syndrome.

Publications

Visuospatial interpolation in typically developing children and in people with Williams Syndrome.

Similar Datasets

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