Longitudinal study of the cognitive development in children with Williams-Beuren syndrome

被引:0
|
作者
Gosch, A
Pankau, R
机构
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 1996年 / 61卷 / 01期
关键词
Williams-Beuren syndrome; longitudinal study; cognitive development;
D O I
10.1002/(SICI)1096-8628(19960102)61:1<26::AID-AJMG5>3.3.CO;2-V
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Crisco [1990: Clin Res 38:536A] reported stability of IQs in a group of 14 children with Williams-Beuren syndrome (WBS) over a Ei-year period and concluded that they display a development rate similar to normal children. The aim of our study was to examine the stability of the development of nonverbal reasoning abilities over a period of 2 years using two methods. We studied 18 children with WBS (9 girls, 9 boys) with a mean age of 6.6 years (range: 4.4-10.6 yr) at year one (T1), and approximately two years later (T2) at the average age of 8.6 years (range: 5.11-12.7 yr), The Columbia Mental Maturity Scale (CMM) and the Draw A Person Test were administered. The results show that the IQs resulting from the Draw A Person Test were stable over the 2-year period (T1: mean IQ = 63.5, T2: mean IQ = 65, t = 0.63), and display a significant correlation between the two methods (r = 0.547, P = 0.01). Furthermore, the correlation between the two tests (CMM and Draw A Person Test) at the second assessment is high and significant (r = 0.56, P = 0.01). The mean IQs at T2 can be classified as mild mental retardation. A notable result is the significant decrease of the IQs according to the CMM (T1: mean IQ = 77, T2: mean IQ = 68, t = 2.69, P = 0.01). These results suggest that the developmental outcome of children with WBS varies in specific areas of cognitive function over a 2-year period. (C) 1996 Wiley-Liss, Inc.
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页码:26 / 29
页数:4
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