Specific cerebellar reductions in children with chromosome 22q11.2 deletion syndrome

被引:41
作者
Bish, Joel P. [1 ]
Pendyal, Akshay
Ding, Lijun
Ferrante, Heather
Nguyen, Vy
McDonald-McGinn, Donna
Zackai, Elaine
Simon, Tony J.
机构
[1] Childrens Hosp Philadelphia, Philadelphia, PA 19104 USA
[2] Ursinus Coll, Dept Neurosci & Psychol, Collegeville, PA 19426 USA
[3] Univ Penn, Philadelphia, PA 19104 USA
[4] Univ Calif Davis, Davis, CA 95616 USA
关键词
chromosome; 22q11.2; VCFS; cerebellum; visuospatial; psychopathology;
D O I
10.1016/j.neulet.2006.02.001
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Children with chromosome 22q11.2 deletion syndrome commonly are found to have morphological brain changes, cognitive impairments, and elevated rates of psychopathology. One of the most commonly and consistently reported brain changes is reduced cerebellar volume. Here, we demonstrate that, in addition to the global cerebellum reductions previously reported, volumetric reductions of the anterior lobule and the vermal region of the neo-cerebellum in the mid-sagittal plane best differentiate children with the deletion from typically developing children. These results suggest that the morphological changes of specific portions of the cerebellum may be an important underlying substrate of cognitive impairments and increased incidence of psychopathology in this group. (c) 2006 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:245 / 248
页数:4
相关论文
共 33 条
[1]   A NEW ROLE FOR THE CEREBELLUM IN COGNITIVE OPERATIONS [J].
AKSHOOMOFF, NA ;
COURCHESNE, E .
BEHAVIORAL NEUROSCIENCE, 1992, 106 (05) :731-738
[2]   The relationship between brain structure and neurocognition in schizophrenia: a selective review [J].
Antonova, E ;
Sharma, T ;
Morris, R ;
Kumari, V .
SCHIZOPHRENIA RESEARCH, 2004, 70 (2-3) :117-145
[3]   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
[4]   Cerebellum in attention-deficit hyperactivity disorder - A morphometric MRI study [J].
Berquin, PC ;
Giedd, JN ;
Jacobsen, LK ;
Hamburger, SD ;
Krain, AL ;
Rapoport, JL ;
Castellanos, FX .
NEUROLOGY, 1998, 50 (04) :1087-1093
[5]   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
[6]   Developmental genetics of the heart [J].
Burn, J ;
Goodship, J .
CURRENT OPINION IN GENETICS & DEVELOPMENT, 1996, 6 (03) :322-325
[7]   HYPOPLASIA OF CEREBELLAR VERMAL LOBULE-VI AND LOBULE-VII IN AUTISM [J].
COURCHESNE, E ;
YEUNGCOURCHESNE, R ;
PRESS, GA ;
HESSELINK, JR ;
JERNIGAN, TL .
NEW ENGLAND JOURNAL OF MEDICINE, 1988, 318 (21) :1349-1354
[8]   Close interrelation of motor development and cognitive development and of the cerebellum and prefrontal cortex [J].
Diamond, A .
CHILD DEVELOPMENT, 2000, 71 (01) :44-56
[9]   PREVALENCE OF 22Q11 MICRODELETIONS IN DIGEORGE AND VELOCARDIOFACIAL SYNDROMES - IMPLICATIONS FOR GENETIC-COUNSELING AND PRENATAL-DIAGNOSIS [J].
DRISCOLL, DA ;
SALVIN, J ;
SELLINGER, B ;
BUDARF, ML ;
MCDONALDMCGINN, DM ;
ZACKAI, EH ;
EMANUEL, BS .
JOURNAL OF MEDICAL GENETICS, 1993, 30 (10) :813-817
[10]   Children and adolescents with velocardiofacial syndrome: A volumetric MRI study [J].
Eliez, S ;
Schmitt, JE ;
White, CD ;
Reiss, AL .
AMERICAN JOURNAL OF PSYCHIATRY, 2000, 157 (03) :409-415