Cognitive modularity and genetic disorders

被引:178
作者
Paterson, SJ
Brown, JH
Gsödl, MK
Johnson, MH
Karmiloff-Smith, A [1 ]
机构
[1] UCL, Inst Child Hlth, Neurocognit Dev Unit, London WC1N 1EH, England
[2] Univ London Univ Coll, Dept Psychol, London WC1E 6BT, England
[3] Birkbeck Coll, Ctr Brain & Cognit Dev, London WC1E 7JL, England
关键词
D O I
10.1126/science.286.5448.2355
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
This study challenges the use of adult neuropsychological models for explaining developmental disorders of genetic origin. When uneven cognitive profiles are found in childhood or adulthood, it is assumed that such phenotypic outcomes characterize infant starting states, and it has been claimed that modules subserving these abilities start out either intact or impaired. Findings from two experiments with infants with Williams syndrome (a phenotype selected to bolster innate modularity claims) indicate a within-syndrome double dissociation: For numerosity judgments, they do well in infancy but poorly in adulthood, whereas for Language, they perform poorly in infancy but well in adulthood. The theoretical and clinical implications of these results could Lead to a shift in focus for studies of genetic disorders.
引用
收藏
页码:2355 / 2358
页数:4
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