Visuospatial and numerical cognitive deficits in children with chromosome 22q11.2 deletion syndrome

被引:110
作者
Simon, TJ
Bearden, CE
Mc-Ginn, DM
Zackai, E
机构
[1] Childrens Hosp Philadelphia, Philadelphia, PA 19104 USA
[2] Univ Penn, Sch Med, Philadelphia, PA 19104 USA
关键词
child; chromosome; 22q11.2; VCFS; parietal lobe; attention; enumeration; magnitude; judgment;
D O I
10.1016/S0010-9452(08)70889-X
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
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.
引用
收藏
页码:145 / 155
页数:11
相关论文
共 58 条
[1]   The neurocognitive phenotype of the 22Q11.2 deletion syndrome: Selective deficit in visual-spatial memory [J].
Bearden, CE ;
Woodin, MF ;
Wang, PP ;
Moss, E ;
McDonald-McGinn, D ;
Zackai, E ;
Emannuel, B ;
Cannon, TD .
JOURNAL OF CLINICAL AND EXPERIMENTAL NEUROPSYCHOLOGY, 2001, 23 (04) :447-464
[2]   DEVELOPMENTAL AND NEUROLOGIC STATUS OF CHILDREN AFTER HEART-SURGERY WITH HYPOTHERMIC CIRCULATORY ARREST OR LOW-FLOW CARDIOPULMONARY BYPASS [J].
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 ;
CASTANEDA, AR ;
WARE, JH ;
NEWBURGER, JW .
NEW ENGLAND JOURNAL OF MEDICINE, 1995, 332 (09) :549-555
[3]   The neurocognitive profile of Williams syndrome: A complex pattern of strengths and weaknesses [J].
Bellugi, U ;
Lichtenberger, L ;
Jones, W ;
Lai, Z ;
St George, M .
JOURNAL OF COGNITIVE NEUROSCIENCE, 2000, 12 :7-29
[4]   Bridging cognition, the brain and molecular genetics: evidence from Williams syndrome [J].
Bellugi, U ;
Lichtenberger, L ;
Mills, D ;
Galaburda, A ;
Korenberg, JR .
TRENDS IN NEUROSCIENCES, 1999, 22 (05) :197-207
[5]  
BENNETTO L, 1996, FRAGILE X SYNDROME D, P210
[6]  
BENTON AL, 1987, MATH DISABILITIES CO, P111
[7]  
Bingham PM, 1997, AM J MED GENET, V74, P538, DOI 10.1002/(SICI)1096-8628(19970919)74:5<538::AID-AJMG17>3.0.CO
[8]  
2-D
[9]  
Chapman RS, 2000, MENT RETARD DEV D R, V6, P84, DOI 10.1002/1098-2779(2000)6:2<84::AID-MRDD2>3.3.CO
[10]  
2-G