Brunger J W, Matthews A L, Smith R H, Robin N H
Departments of Genetics, Case Western Reserve University School of Medicine, University Hospitals of Cleveland, Cleveland, Ohio, USA.
Laryngoscope. 2001 Apr;111(4 Pt 1):715-8. doi: 10.1097/00005537-200104000-00027.
Today, genetic testing is an option for individuals who have deafness and hard-of-hearing conditions (D/HOH) and their families for diagnosis and carrier detection. As more and more D/HOH genes are identified, genetic testing will become commonplace. However, genetic testing is different from other tests that physicians commonly order and therefore should be conducted differently. The objective of this study was to determine the best manner in which to conduct genetic testing for individuals who have D/HOH. Numerous studies have shown that pretest and post-test genetic counseling is beneficial for patients and families undergoing genetic testing for a variety of conditions. The need for counseling was emphasized by our recently completed study in which we found that the majority of individuals whose children had genetic testing for D/HOH had a poor understanding of many genetic issues concerning recurrence risks for D/HOH and the meaning of the test results. We think that genetic counseling should be an integral part of genetic testing for individuals who have D/HOH.
如今,基因检测对于患有耳聋及听力障碍疾病(D/HOH)的个人及其家属来说,是一种用于诊断和携带者检测的选择。随着越来越多的D/HOH基因被识别出来,基因检测将变得普遍。然而,基因检测与医生通常所安排的其他检测不同,因此其实施方式也应有所不同。本研究的目的是确定对患有D/HOH的个体进行基因检测的最佳方式。大量研究表明,检测前和检测后的基因咨询对接受各种疾病基因检测的患者及其家属有益。我们最近完成的一项研究强调了咨询的必要性,在该研究中我们发现,大多数其子女接受D/HOH基因检测的个体对许多与D/HOH复发风险及检测结果含义相关的基因问题了解甚少。我们认为,基因咨询应该成为患有D/HOH个体基因检测不可或缺的一部分。