Identifying neurocognitive phenotypes in autism

被引:281
作者
Tager-Flusberg, H [1 ]
Joseph, RM [1 ]
机构
[1] Boston Univ, Sch Med, Dept Anat & Neurobiol, Lab Dev Cognt Neurosci, Boston, MA 02118 USA
关键词
autism; phenotype; cognitive profile; specific language impairment; language; macrocephaly;
D O I
10.1098/rstb.2002.1198
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Autism is a complex disorder that is heterogeneous both in its phenotypic expression and its etiology. The search for genes associated with autism and the neurobiological mechanisms that underlie its behavioural symptoms has been hampered by this heterogeneity. Recent studies indicate that within autism, there may be distinct subgroups that can be defined based on differences in neurocognitive profiles. This paper presents evidence for two kinds of subtypes in autism that are defined on, the basis of language profiles and on the basis of cognitive profiles. The implications for genetic and neurobiological studies of these subgroups are discussed, with special reference to evidence relating these cognitive phenotypes to volumetric studies of brain size and organization in autism.
引用
收藏
页码:303 / 314
页数:12
相关论文
共 110 条
[1]   Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2 [J].
Amir, RE ;
Van den Veyver, IB ;
Wan, M ;
Tran, CQ ;
Francke, U ;
Zoghbi, HY .
NATURE GENETICS, 1999, 23 (02) :185-188
[2]  
[Anonymous], 1993, INT CLASS DIS
[3]  
[Anonymous], UNDERSTANDING OTHER
[4]   Autism: The phenotype in relatives [J].
Bailey, A ;
Palferman, S ;
Heavey, L ;
Le Couteur, A .
JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS, 1998, 28 (05) :369-392
[5]  
Bailey A, 1998, HUM MOL GENET, V7, P571
[6]   Autism: Towards an integration of clinical, genetic, neuropsychological, and neurobiological perspectives [J].
Bailey, A ;
Phillips, W ;
Rutter, M .
JOURNAL OF CHILD PSYCHOLOGY AND PSYCHIATRY, 1996, 37 (01) :89-126
[7]   AUTISM AS A STRONGLY GENETIC DISORDER - EVIDENCE FROM A BRITISH TWIN STUDY [J].
BAILEY, A ;
LECOUTEUR, A ;
GOTTESMAN, I ;
BOLTON, P ;
SIMONOFF, E ;
YUZDA, E ;
RUTTER, M .
PSYCHOLOGICAL MEDICINE, 1995, 25 (01) :63-77
[8]  
BallabanGil K, 1997, PEDIATR NEUROL, V16, P353, DOI 10.1016/S0887-8994(97)90140-5
[9]  
Barrett S, 1999, AM J MED GENET, V88, P609
[10]   COMPARATIVE STUDY OF INFANTILE AUTISM AND SPECIFIC DEVELOPMENTAL RECEPTIVE LANGUAGE DISORDER .1. CHILDREN [J].
BARTAK, L ;
RUTTER, M ;
COX, A .
BRITISH JOURNAL OF PSYCHIATRY, 1975, 126 (FEB) :127-145