A cognitive characterization of dyscalculia in Turner syndrome

被引:88
作者
Bruandet, M
Molko, N
Cohen, L
Dehaene, S
机构
[1] CEA, Serv Hosp Frederic Joliot, INSERM, DRM,DSV,Unit 562, F-91401 Orsay, France
[2] Hop La Pitie Salpetriere, Serv Urgences Cerebro Vasc, AP HP, Paris, France
[3] Hop La Pitie Salpetriere, Inst Neurol, AP HP, Paris, France
关键词
developmental dyscalculia; Turner Ulrich syndrome; estrogen; X chromosome; parietal;
D O I
10.1016/j.neuropsychologia.2003.08.007
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
Current theories of number processing postulate that the human abilities for arithmetic are based on cerebral circuits that are partially laid down under genetic control and later modified by schooling and education. This view predicts the existence of genetic diseases that interfere specifically with components of the number system. Here, we investigate whether Turner syndrome (TS) corresponds to this definition. TS is a genetic disorder which affects one woman in 2500 and is characterized by partial or complete absence of one X chromosome. In addition to well-characterized physical and hormonal dysfunction, TS patients exhibit cognitive deficits including dyscalculia. We tested 12 women with Turner syndrome and 13 control subjects on a cognitive battery including arithmetical tests (addition, subtraction, multiplication, division) as well as tests of the understanding of numerosity and quantity (cognitive estimation, estimation, comparison, bisection, subitizing/counting). Impairments were observed in cognitive estimation, subitizing, and calculation. We examine whether these deficits can be attributed to a single source, and discuss the possible implications of hormonal and genetic factors in the neuropsychological profile of TS patients. (C) 2003 Elsevier Ltd. All rights reserved.
引用
收藏
页码:288 / 298
页数:11
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