Understanding autism: insights from mind and brain

被引:238
作者
Hill, EL [1 ]
Frith, U [1 ]
机构
[1] UCL, Inst Cognit Neurosci, London WC1N 3AR, England
关键词
autism; Asperger syndrome; theory of mind; weak central coherence; executive dysfunction; phenotype;
D O I
10.1098/rstb.2002.1209
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Autism is a developmental disorder characterized by impaired social interaction and communication as well as repetitive behaviours and restricted interests. The consequences of this disorder for everyday life adaptation are extremely variable. The general public is now more aware of the high prevalence of this lifelong disorder, with ca. 0.6% of the population being affected. However, the signs and symptoms of autism are still puzzling. Since a biological basis of autism was accepted, approaches from developmental cognitive neuroscience have been applied to further our understanding of the autism spectrum. The study of the behavioural and underlying cognitive deficits in autism has advanced ahead of the study of the underlying brain abnormalities and of the putative genetic mechanisms. However, advances in these fields are expected as methodological difficulties are overcome. In this paper, recent developments in the field of autism are outlined. In particular, we review the findings of the three main neuro-cognitive theories of autism: theory-of-mind deficit, weak central coherence and executive dysfunction.
引用
收藏
页码:281 / 289
页数:9
相关论文
共 98 条
  • [1] The neuroanatomy of autism:: a voxel-based whole brain analysis of structural scans
    Abell, F
    Krams, M
    Ashburner, J
    Passingham, R
    Friston, KJ
    Frackowiak, R
    Happé, F
    Frith, C
    Frith, U
    [J]. NEUROREPORT, 1999, 10 (08) : 1647 - 1651
  • [2] [Anonymous], 1997, A real person: Life on the outside
  • [3] [Anonymous], AUTISM EXECUTIVE DIS
  • [4] Asperger Hans., 1944, Autism and Asperger Syndrome, P37
  • [5] MRI volumes of amygdala and hippocampus in non-mentally retarded autistic adolescents and adults
    Aylward, EH
    Minshew, NJ
    Goldstein, G
    Honeycutt, NA
    Augustine, AM
    Yates, KO
    Barta, PE
    Pearlson, GD
    [J]. NEUROLOGY, 1999, 53 (09) : 2145 - 2150
  • [6] Autism: The phenotype in relatives
    Bailey, A
    Palferman, S
    Heavey, L
    Le Couteur, A
    [J]. JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS, 1998, 28 (05) : 369 - 392
  • [7] Bailey A, 1998, HUM MOL GENET, V7, P571
  • [8] AUTISM AS A STRONGLY GENETIC DISORDER - EVIDENCE FROM A BRITISH TWIN STUDY
    BAILEY, A
    LECOUTEUR, A
    GOTTESMAN, I
    BOLTON, P
    SIMONOFF, E
    YUZDA, E
    RUTTER, M
    [J]. PSYCHOLOGICAL MEDICINE, 1995, 25 (01) : 63 - 77
  • [9] A clinicopathological study of autism
    Bailey, A
    Luthert, P
    Dean, A
    Harding, B
    Janota, I
    Montgomery, M
    Rutter, M
    Lantos, P
    [J]. BRAIN, 1998, 121 : 889 - 905
  • [10] A screening instrument for autism at 18 months of age: A 6-year follow-up study
    Baird, G
    Charman, T
    Baron-Cohen, S
    Cox, A
    Swettenham, J
    Wheelwright, S
    Drew, A
    [J]. JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY, 2000, 39 (06) : 694 - 702