Visuospatial and numerical cognitive deficits in children with chromosome 22q11.2 deletion syndrome
- PMID: 15714897
- PMCID: PMC4318636
- DOI: 10.1016/s0010-9452(08)70889-x
Visuospatial and numerical cognitive deficits in children with chromosome 22q11.2 deletion syndrome
Abstract
This article presents some of the earliest evidence of visuospatial and numerical cognitive deficits in children with the chromosome 22q11.2 deletion syndrome; a common but ill-understood genetic disorder resulting in medical complications, cognitive impairment, and brain morphologic changes. Relative to a group of typically developing controls, deleted children performed more poorly on tests of visual attentional orienting, visual enumeration and relative numerical magnitude judgment. Results showed that performance deficits in children with the deletion could not be explained by a global deficit in psychomotor speed. Instead, our findings are supportive of the hypothesis that visuospatial and numerical deficits in children with the chromosome 22q11.2 deletion are due, at least in part, to posterior parietal dysfunction.
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References
-
- Bearden CE, Woodin MF, Wang PP, Moss E, McDonald-McGinn D, Zackai E, Emannuel B, Cannon TD. The neurocognitive phenotype of the 22q11.2 deletion syndrome: Selective deficit in visual-spatial memory. Journal of Clinical and Experimental Neuropsychology. 2001;23:447–64. - PubMed
-
- Bellinger DC, Jonas RA, Rappaport LA, Wypij D, Wernovsky G, Kuban KCK, Barnes PD, Holmes GL, Hickey PR, Strand RD, Walsh AZ, Helmers SL, Constantinou JE, Carrazana EJ, Mayer JE, Hanley FL, Casteneda AR, Ware JH, Newburger JW. Developmental and neurologic status of children after heart surgery with hypothermic circulatory arrest or low-flow cardiopulmonary bypass. New England Journal of Medicine. 1995;332:549–555. - PubMed
-
- Bellugi U, Lichtenberger L, Jones W, Lai Z, St. George M. The neurocognitive profile of Williams syndrome: A complex pattern of strengths and weaknesses. Journal of Cognitive Neuroscience. 2000;12:7–29. - PubMed
-
- Bellugi U, Lichtenberger L, Mills D, Galaburda A, Korenberg JR. Bridging cognition, the brain and molecular genetics: Evidence from Williams syndrome. Trends in Neuroscience. 1999;22:197–207. - PubMed
-
- Bennetto L, Pennington BF. The neuropsychology of fragile x syndrome. In: Hagerman RJ, Cronister A, editors. Fragile X Syndrome: Diagnosis, Treatment and Research. Johns Hopkins University Press; Baltimore: 1996. pp. 210–248.
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