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自闭症谱系障碍的遗传学:综述与临床意义。

Genetics of autistic disorders: review and clinical implications.

机构信息

Department of Child and Adolescent Psychiatry, Psychosomatics, and Psychotherapy, Johann Wolfgang Goethe-University, Deutschordenstrasse 50, Frankfurt am Main, Germany.

出版信息

Eur Child Adolesc Psychiatry. 2010 Mar;19(3):169-78. doi: 10.1007/s00787-009-0076-x. Epub 2009 Nov 26.

Abstract

Twin and family studies in autistic disorders (AD) have elucidated a high heritability of AD. In this literature review, we will present an overview on molecular genetic studies in AD and highlight the most recent findings of an increased rate of copy number variations in AD. An extensive literature search in the PubMed database was performed to obtain English published articles on genetic findings in autism. Results of linkage, (genome wide) association and cytogenetic studies are presented, and putative aetiopathological pathways are discussed. Implications of the different genetic findings for genetic counselling and genetic testing at present will be described. The article ends with a prospectus on future directions.

摘要

对自闭症谱系障碍(ASD)的双胞胎和家族研究表明,ASD 的遗传性很高。在这篇文献综述中,我们将概述 ASD 的分子遗传学研究,并强调最近发现的 ASD 中拷贝数变异率升高的研究结果。在 PubMed 数据库中进行了广泛的文献检索,以获得关于自闭症遗传发现的英文已发表文章。目前呈现了连锁、(全基因组)关联和细胞遗传学研究的结果,并讨论了可能的发病机制途径。本文还描述了不同遗传发现对目前遗传咨询和基因检测的影响。文章最后展望了未来的研究方向。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9fbc/2839494/58a7ffa7c1b1/787_2009_76_Fig1_HTML.jpg

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