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近亲结婚的产前和孕前遗传咨询:近亲夫妇的期望、经历和观点。

Prenatal and preconception genetic counseling for consanguinity: Consanguineous couples' expectations, experiences, and perspectives.

作者信息

Thain Emily, Shuman Cheryl, Miller Kristen, Sappleton Karen, Myles-Reid Diane, Chitayat David, Gibbons Clare

机构信息

Department of Molecular Genetics, University of Toronto, Toronto, ON, Canada.

Division of Clinical and Metabolic Genetics, Department of Pediatrics, The Hospital for Sick Children, Toronto, ON, Canada.

出版信息

J Genet Couns. 2019 Oct;28(5):982-992. doi: 10.1002/jgc4.1150. Epub 2019 Jul 16.

Abstract

Consanguinity, the union between two individuals who are related as second cousins or closer, is a long-standing and respected tradition in many communities. Although there are social and economic benefits of consanguineous unions, offspring are at increased risk of having an inherited genetic condition or congenital anomaly. Genetic counseling services for consanguinity are available to couples at many centers. However, little is known about patient expectations of and experiences with genetic counseling for this indication, or their perspectives on genetic screening relevant to family planning, such as expanded carrier screening (ECS). This exploratory qualitative study involved interviews with 13 individuals who had recently received preconception or prenatal genetic counseling for consanguinity at a single center. We sought to gain insight into their expectations for the genetic counseling session, experiences discussing family history and reproductive risks with the genetic counselor, and views on ECS. Interview transcripts were analyzed using an interpretive descriptive approach. Data analysis revealed three main themes: (a) anticipation balances apprehension before the appointment; (b) genetic counseling reduces anxiety and empowers; and (c) the need for wider information dissemination about consanguinity-related risks and genetic services. Our findings support the personal utility of genetic counseling for consanguinity and demonstrate the need for increased visibility and access to genetics information, counseling, and testing relevant to this patient population.

摘要

近亲结婚,即两个具有二级表亲或更近亲缘关系的个体之间的结合,在许多社区都是一个由来已久且备受尊重的传统。尽管近亲结婚有社会和经济方面的益处,但后代患遗传性疾病或先天性异常的风险会增加。许多中心都为近亲结婚的夫妇提供遗传咨询服务。然而,对于患者对这种遗传咨询的期望和体验,或者他们对与计划生育相关的基因筛查(如扩展携带者筛查,ECS)的看法,我们知之甚少。这项探索性的定性研究对13名最近在单一中心接受过近亲结婚孕前或产前遗传咨询的个体进行了访谈。我们试图深入了解他们对遗传咨询 session 的期望、与遗传咨询师讨论家族史和生殖风险的经历,以及对扩展携带者筛查的看法。访谈记录采用解释性描述方法进行分析。数据分析揭示了三个主要主题:(a) 在预约前,期待与担忧并存;(b) 遗传咨询减轻焦虑并赋予力量;(c) 需要更广泛地传播与近亲结婚相关风险和遗传服务的信息。我们的研究结果支持了近亲结婚遗传咨询的个人效用,并表明需要提高与该患者群体相关的遗传学信息、咨询和检测的可见性和可及性。

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