Domain specific attentional impairments in children with chromosome 22q11.2 deletion syndrome

被引:30
作者
Bish, Joel P.
Chiodo, Renee
Mattei, Victoria
Simon, Tony J.
机构
[1] Ursinus Coll, Dept Neurosci, Collegeville, PA 19426 USA
[2] Childrens Hosp Philadelphia, Philadelphia, PA 19104 USA
[3] Univ Calif Davis, Davis, CA 95616 USA
关键词
22q; 11.2; inhibition of return; spatial attention; object attention;
D O I
10.1016/j.bandc.2007.03.007
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
One of the defining cognitive characteristics of the chromosome 22q deletion syndrome (DS22q11.2) is visuospatial processing impairments. The purpose of this study was to investigate and extend the specific attentional profile of children with this disorder using both an object-based attention task and an inhibition of return task. A group of children with the disorder was compared in these tasks with a group of age-matched typically developing children. The children with DS22q11.2 demonstrated impaired spatially based orienting which is consistent with previous findings in this group. Strikingly, the children with DS22q11.2 also demonstrated an improved ability to use object-based cues, relative to the typically developing group. Finally, the children with DS22q11.2 demonstrated an intact inhibition of return system, however, it appears to be delayed developmentally. (C) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:265 / 273
页数:9
相关论文
共 38 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]   Specific cerebellar reductions in children with chromosome 22q11.2 deletion syndrome [J].
Bish, Joel P. ;
Pendyal, Akshay ;
Ding, Lijun ;
Ferrante, Heather ;
Nguyen, Vy ;
McDonald-McGinn, Donna ;
Zackai, Elaine ;
Simon, Tony J. .
NEUROSCIENCE LETTERS, 2006, 399 (03) :245-248
[3]   Maladaptive conflict monitoring as evidence for executive dysfunction in children with chromosome 22q11.2 deletion syndrome [J].
Bish, JP ;
Ferrante, SM ;
McDonald-McGinn, D ;
Zackai, E ;
Simon, TJ .
DEVELOPMENTAL SCIENCE, 2005, 8 (01) :36-43
[4]   Thalamic reductions in children with chromosome 22qll.2 deletion syndrome [J].
Bish, JP ;
Nguyen, V ;
Ding, LJ ;
Ferrante, S ;
Simon, TJ .
NEUROREPORT, 2004, 15 (09) :1413-1415
[5]   Developmental genetics of the heart [J].
Burn, J ;
Goodship, J .
CURRENT OPINION IN GENETICS & DEVELOPMENT, 1996, 6 (03) :322-325
[6]   CONOTRUNCAL ANOMALY FACE SYNDROME IS ASSOCIATED WITH A DELETION WITHIN CHROMOSOME-22Q11 [J].
BURN, J ;
TAKAO, A ;
WILSON, D ;
CROSS, I ;
MOMMA, K ;
WADEY, R ;
SCAMBLER, P ;
GOODSHIP, J .
JOURNAL OF MEDICAL GENETICS, 1993, 30 (10) :822-824
[7]   Temporal perception in velo-cardio-facial syndrome [J].
Debbané, M ;
Glaser, B ;
Gex-Fabry, M ;
Eliez, S .
NEUROPSYCHOLOGIA, 2005, 43 (12) :1754-1762
[8]  
DRISCOLL DA, 1992, AM J HUM GENET, V50, P924
[10]   SHIFTING VISUAL-ATTENTION BETWEEN OBJECTS AND LOCATIONS - EVIDENCE FROM NORMAL AND PARIETAL LESION SUBJECTS [J].
EGLY, R ;
DRIVER, J ;
RAFAL, RD .
JOURNAL OF EXPERIMENTAL PSYCHOLOGY-GENERAL, 1994, 123 (02) :161-177