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家长对儿童耳聋基因检测的态度。

Parental attitudes toward genetic testing for pediatric deafness.

作者信息

Brunger J W, Murray G S, O'Riordan M, Matthews A L, Smith R J, Robin N H

机构信息

Department of Genetics, Case Western Reserve University School of Medicine, University Hospitals of Cleveland, Cleveland, OH, USA.

出版信息

Am J Hum Genet. 2000 Dec;67(6):1621-5. doi: 10.1086/316901. Epub 2000 Nov 2.

Abstract

Recent molecular genetic advances have resulted in genetic testing becoming an option for deaf individuals and their families. However, there is little information about the interest in such testing. To investigate this issue, parents with normal hearing who have one or more deaf children were surveyed about their attitudes toward diagnostic, carrier, and prenatal genetic testing for deafness. This population was chosen because it represents the majority of individuals who are encountered in clinical practice, given that 90%-95% of deaf individuals are born to persons with normal hearing. Of 328 surveys distributed, 96 were completed and returned. Of the respondents, 96% recorded a positive attitude toward genetic testing for deafness, including prenatal testing, although none would use this information to terminate an affected pregnancy. All respondents had a poor understanding of genetics, with 98% both incorrectly estimating the recurrence risk of deafness and misunderstanding the concept of inheritance. Notably, these findings were similar in the group who had had genetic testing for their children and in the group who had not, suggesting either that the parents who received genetic testing did not receive genetic counseling or that the counseling was not effective. On the basis of these results, it was concluded that this population is interested in the use of genetic testing and that testing should not be done without first providing formal genetic counseling. Appropriate counseling can help parents to understand the risks, benefits, and limitations of genetic testing.

摘要

最近分子遗传学的进展使基因检测成为聋人及其家庭的一种选择。然而,关于这种检测的兴趣方面的信息却很少。为了调查这个问题,对有一个或多个失聪子女的听力正常的父母进行了调查,询问他们对耳聋的诊断性、携带者及产前基因检测的态度。选择这一人群是因为考虑到90%-95%的聋人出生于听力正常的人,他们代表了临床实践中遇到的大多数个体。在分发的328份调查问卷中,96份被填写并返回。在受访者中,96%的人对耳聋基因检测,包括产前检测持积极态度,尽管没有人会利用这些信息终止受影响的妊娠。所有受访者对遗传学的了解都很差,98%的人既错误估计了耳聋的复发风险,又误解了遗传的概念。值得注意的是,在为子女进行过基因检测的组和未进行过基因检测的组中,这些发现相似,这表明接受基因检测的父母要么没有接受遗传咨询,要么咨询没有效果。基于这些结果,得出的结论是,这一人群对基因检测的应用感兴趣,并且在没有首先提供正式遗传咨询的情况下不应进行检测。适当的咨询可以帮助父母了解基因检测的风险、益处和局限性。

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