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自闭症:亲属中的表型。

Autism: the phenotype in relatives.

作者信息

Bailey A, Palferman S, Heavey L, Le Couteur A

机构信息

Medical Research Council Child Psychiatry Unit, Institute of Psychiatry, London, United Kingdom.

出版信息

J Autism Dev Disord. 1998 Oct;28(5):369-92. doi: 10.1023/a:1026048320785.

Abstract

There is broad agreement that genetic influences are central in the development of idiopathic autism. Whether relatives manifest genetically related milder phenotypes, and if so how these relate to autism proper, has proved a more contentious issue. A review of the relevant studies indicates that relatives are sometimes affected by difficulties that appear conceptually related to autistic behaviors. These range in severity from pervasive developmental disorders to abnormalities in only one area of functioning, and possibly extend to related personality traits. Issues involved in clarifying the components of milder phenotypes and their relationship to autism are outlined.

摘要

人们普遍认为,遗传影响在特发性自闭症的发展中起着核心作用。亲属是否表现出与遗传相关的较轻微表型,如果是,这些表型与自闭症本身有何关系,这已被证明是一个更具争议性的问题。对相关研究的综述表明,亲属有时会受到一些在概念上与自闭症行为相关的困难的影响。这些困难的严重程度从广泛性发育障碍到仅在一个功能领域出现异常,甚至可能延伸到相关的人格特质。本文概述了在阐明较轻微表型的组成部分及其与自闭症的关系时所涉及的问题。

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