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首页> 外文期刊>Journal of genetic counseling >Department of Medical Genetics, University Medical Center, Utrecht, The Netherlands
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Department of Medical Genetics, University Medical Center, Utrecht, The Netherlands

机译:荷兰乌得勒支大学医学中心医学遗传学系

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摘要

Fragile X syndrome is primarily due to a CGG repeat expansion found in the FMR1 X-linked gene. In a previous study, we conducted focus groups with women to assess their attitudes towards fragile X carrier screening. In this follow-up study, we conducted in-depth interviews of general population reproductive-age women who were identified as carriers. We explored their attitudes toward testing for carrier status of the fragile X mutation. These women underwent screening primarily to participate in a research project rather than in search of a diagnosis for specific symptoms. As such, these women were wholly unprepared for positive carrier results. Their responses about their results and carrier screening, in many cases, were being worked out over the course of the interview itself. The most salient finding of this work is the apparent lack of relevance of carrier status to these women. Many expressed that although the information could be relevant in the future, it is not relevant at this stage of their lives in terms of family planning (either with respect to having unaffected offspring or to premature ovarian failure) and personal relationships. Although issues of abortion seemed prominent in the focus groups, we found that carrier status did not have an apparent effect on women’s attitudes about termination. We hypothesize this may be related to the fact that women had not processed their new carrier status and had not related it to previously-formed personal opinions. The findings of this work have significant implications for genetic counseling and population screening. Genetic counselors should be mindful that general population women may not recognize the immediate importance of their carrier status even when literature is provided and discussed prior to providing a sample. As part of comprehensive genetic counseling, counselors should identify the reproductive life stage of the woman receiving the new information and help her identify when this information would be more meaningful in her life. Counselors can assist in setting up a personalized road map with specific types of services that will be more applicable to the woman as her carrier status becomes more relevant.
机译:脆性X综合征主要归因于在FMR1 X连锁基因中发现的CGG重复扩增。在先前的研究中,我们与女性进行了焦点小组讨论,以评估她们对脆弱的X携带者筛查的态度。在这项后续研究中,我们对被确定为携带者的一般人口育龄妇女进行了深入访谈。我们探索了他们对测试脆性X突变携带者状态的态度。这些妇女进行筛查主要是为了参加研究项目,而不是为了寻找特定症状的诊断。因此,这些妇女完全没有为阳性携带者结果做好准备。在许多情况下,他们是在访谈本身的过程中就其对结果和携带者筛查的反应做出的。这项工作最显着的发现是,这些妇女显然缺乏携带者身份。许多人表示,尽管这些信息将来可能有用,但就其计划生育(不影响后代或卵巢早衰而言)和人际关系而言,在现阶段的生活中并不重要。尽管堕胎问题在焦点小组中似乎很突出,但我们发现携带者的身份并没有对妇女的终止态度产生明显影响。我们假设这可能与以下事实有关:女性没有处理其新的携带者身份,也没有将其与先前形成的个人意见相关。这项工作的发现对遗传咨询和人口筛选具有重要意义。遗传咨询师应注意,即使在提供样本之前提​​供了文献并进行了讨论,普通女性也可能不会意识到其携带者身份的紧迫性。作为全面遗传咨询的一部分,咨询员应确定接受新信息的妇女的生殖生命阶段,并帮助她确定该信息何时对她的生活更有意义。辅导员可以协助建立个性化的路线图,其中包含特定类型的服务,随着女性的携带者身份变得越来越重要,该路线图将更适用于该女性。

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