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染色体微阵列分析解读:儿童神经科医生该如何应对?

Chromosomal microarray interpretation: what is a child neurologist to do?

机构信息

Division of Pediatric and Developmental Neurology, Department of Neurology, Washington University School of Medicine, Campus Box 8111, 660 South Euclid Avenue, St. Louis, MO 63110-1093, USA.

出版信息

Pediatr Neurol. 2009 Dec;41(6):391-8. doi: 10.1016/j.pediatrneurol.2009.05.003.

Abstract

The chromosomal microarray now plays a central role in the evaluation of children with neurologic developmental disorders, including global developmental delay, mental retardation, and increasingly also autistic spectrum disorders. As arrays become more sophisticated and their use more widespread, the child neurologist is likely to encounter abnormal chromosomal microarray results. The interpretation of such data is not always straightforward. This review article discusses in a practical manner the nature of chromosomal microarray results, describes an algorithm to help the child neurologist navigate a variety of testing scenarios, and proposes a standardized system for ranking array data based on levels of evidence of genotype-phenotype correlation.

摘要

染色体微阵列分析在神经发育障碍儿童的评估中起着核心作用,包括全面发育迟缓、智力障碍,以及越来越多的自闭症谱系障碍。随着微阵列技术的不断发展和应用的日益广泛,儿童神经科医生可能会遇到异常的染色体微阵列结果。这些数据的解释并不总是那么简单。本文以实用的方式讨论了染色体微阵列结果的性质,描述了一种帮助儿童神经科医生处理各种测试情况的算法,并提出了一种基于基因型-表型相关性证据水平的标准化阵列数据分级系统。

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