High phenotypic correlations among siblings with autism and pervasive developmental disorders

被引:0
|
作者
Szatmari, P
Jones, MB
Holden, J
Bryson, S
Mahoney, W
Tuff, L
MacLean, J
White, B
Bartolucci, G
Schutz, C
Robinson, P
Hoult, L
机构
[1] MCMASTER UNIV, DEPT PSYCHIAT, HAMILTON, ON, CANADA
[2] MCMASTER UNIV, DEPT PEDIAT, HAMILTON, ON, CANADA
[3] MCMASTER UNIV, DEPT BIOL, HAMILTON, ON, CANADA
[4] QUEENS UNIV, DEPT PSYCHIAT, KINGSTON, ON K7L 3N6, CANADA
[5] YORK UNIV, DEPT PSYCHOL, N YORK, ON M3J 1P3, CANADA
[6] PENN STATE UNIV, DEPT BEHAV SCI, HERSHEY, PA USA
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 1996年 / 67卷 / 04期
关键词
autism; genetics; family studies;
D O I
10.1002/(SICI)1096-8628(19960726)67:4<354::AID-AJMG7>3.0.CO;2-M
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The objective of this study was to examine familial factors influencing clinical variation in sibships that contained at least 2 children affected with autism or another form of pervasive developmental disorder (PDD), The sample included a total of 60 families, 23 with multiple cases of PDD and 37 with a single affected child, Measurements of IQ, adaptive behaviors in socialization and communication, and autistic symptoms were taken on all affected children, A high intraclass correlation, especially on IQ and an index of social behaviors, was observed between affected children from the same family, In contrast, low correlations were observed on measurements of IQ and adaptive behavior between affected and unaffected children from the same family, These data indicate that variation in severity of PDD is influenced by familial, and probably genetic, mechanisms, The results are discussed in relation to current theories on the genetics of autism and the heritable mechanisms underlying variations in clinical severity. (C) 1996 Wiley-Liss, Inc.
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页码:354 / 360
页数:7
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