GENETIC LATENT STRUCTURE-ANALYSIS OF DYSMORPHOLOGY IN ATTENTION DEFICIT DISORDER

被引:55
作者
DEUTSCH, CK
MATTHYSSE, S
SWANSON, JM
FARKAS, LG
机构
[1] HOSP SICK CHILDREN,PLAST SURG RES LAB,LONDON WC1N 3JH,ENGLAND
[2] UNIV TORONTO,FAC MED,DEPT SURG,TORONTO M5S 1A1,ONTARIO,CANADA
[3] HARVARD UNIV,SCH MED,DEPT PSYCHIAT,BOSTON,MA 02115
[4] HARVARD UNIV,MCLEAN HOSP,SCH MED,DEPT PSYCHIAT,BELMONT,MA 02178
[5] UNIV CALIF IRVINE,CALIF COLL MED,DEPT PEDIAT,CHILD DEV CLIN,IRVINE,CA 92717
关键词
attention-deficit hyperactivity disorder; dysmorphology; genetics; minor physical anomalies;
D O I
10.1097/00004583-199003000-00006
中图分类号
B844 [发展心理学(人类心理学)];
学科分类号
040202 ;
摘要
Dysmorphology—in the form of minor physical anomalies—has been frequently reported in children with attention deficit disorder (ADD). The authors report an overrepresentation of minor physical anomalies in both ADD probands and their first-degree relatives. Further, ADD probands who are not dysmorphic have non-ADD relatives who are dysmorphic; this familial pattern suggests that a single underlying factor may influence transmission of both traits. A genetic latent structure model was fit to these data to describe the factor's mode of transmission. In this analysis, an autosomal dominant model emerged. Successfully fitting this model is not equivalent to testing the validity of the model itself. Meaningful tests of the model will require larger samples than available at present, and would benefit from diagnostic refinement of the ADD and dysmorphic phenotypes. © 1990, The American Academy of Child and Adolescent Psychiatry. All rights reserved.
引用
收藏
页码:189 / 194
页数:6
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