METACARPOPHALANGEAL PATTERN PROFILE ANALYSIS IN WILLIAMS-SYNDROME

被引:9
作者
BURNS, MA
MCLEOD, DR
LINTON, LR
BUTLER, MG
机构
[1] ALBERTA CHILDRENS PROV GEN HOSP,RES CTR,1820 RICHMOND RD SW,CALGARY T2T 5C7,ALBERTA,CANADA
[2] UNIV CALGARY,SCH MED,CALGARY T2N 1N4,ALBERTA,CANADA
[3] UNIV CALGARY,DEPT BIOL SCI,CALGARY T2N 1N4,ALBERTA,CANADA
[4] VANDERBILT UNIV,MED CTR,SCH MED,DEPT PEDIAT,NASHVILLE,TN 37232
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 1993年 / 47卷 / 04期
关键词
WILLIAMS SYNDROME; METACARPOPHALANGEAL PATTERN PROFILE (MCPP); COMPUTER-AUTOMATED METACARPOPHALANGEAL PROFILE SYSTEM (CAMPS); DISCRIMINANT ANALYSIS;
D O I
10.1002/ajmg.1320470407
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Many patients with Williams syndrome (WS) are not diagnosed until they are old enough to demonstrate the characteristic personality and facial changes. A number of these changes are quite subtle and none of them is present in all affected individuals. The cause of WS remains obscure and consequently, there are no cytogenetic, biochemical, or molecular studies to help in the diagnosis of patients in whom the diagnosis is uncertain. We have generated a mean WS metacarpophalangeal pattern profile (MCPP) on 21 clinically diagnosed individuals with WS. This mean syndrome profile shows that WS hands are smaller than average age-matched control hands and that the distal phalanx of the thumb is disproportionately large with respect to the rest of the hand. A mathematical model, which effectively discriminates WS patients from unaffected control individuals, was developed using discriminant analysis of the MCPP data. Of the 21 WS patients classified by this method, only 2 were misclassified as ''normal.'' Similarly, 2 of the 24 control individuals were misclassified as ''WS,'' yielding an overall successful classification rate of 91%. (C) 1993 Wiley-Liss, Inc.
引用
收藏
页码:471 / 474
页数:4
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