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表达主义对产前检测的反对:患有遗传疾病的家庭的经历。

The expressivist objection to prenatal testing: the experiences of families living with genetic disease.

机构信息

Warwick Medical School, Gibbet Hill Road, Coventry CV4 7AL, UK.

出版信息

Soc Sci Med. 2014 Apr;107:18-25. doi: 10.1016/j.socscimed.2014.02.025. Epub 2014 Feb 14.

Abstract

The expressivist objection to prenatal testing is acknowledged as a significant critique of prenatal testing practices most commonly advanced by disability rights supporters. Such writers argue that prenatal testing and selective termination practices are objectionable as they express disvalue not only of the foetus being tested, but also of disabled people as a whole, by focusing exclusively on the disabling trait. While the objection has been widely critiqued on the basis of its theoretical incoherence, this paper highlights the way in which it, nevertheless, is a significant mediator in decisions around the use of reproductive genetic technologies. By drawing on 41 in-depth qualitative interviews (drawn from a sample of 61) conducted in the UK between 2007 and 2009 with families and individuals living with a genetic disease, Spinal Muscular Atrophy (SMA), this paper highlights the ways in which expressivist objections feature prominently in the reproductive decisions of families living with SMA and the significant emotional burden they represent. While the literature on the expressivist objection has focused on the reproductive decisions of those undergoing prenatal testing for a condition of which they have little (or no) prior knowledge, the context of intimate familial relationships and extensive experience with the tested-for condition fundamentally alters the nature and impact of expressivist objections within families living with an inheritable condition. By focussing on the reproductive decisions of families living with SMA and their strategic management of the expressivist objection, this paper will address the call, made primarily by disability rights supporters, for 'experientially based' (as opposed to medical) information about the tested-for disability to be made available to would-be parents considering selective termination. It will be argued that parents' experiential knowledge of the tested-for disability can, in fact, amplify expressivist objections to prenatal testing, and thus paradoxically constrain, rather than facilitate, reproductive decisions.

摘要

表达主义者反对产前检测被认为是对残疾权利支持者最常提出的产前检测实践的重要批评。这些作家认为,产前检测和选择性终止实践是令人反感的,因为它们不仅表达了对被检测胎儿的不重视,而且还表达了对整个残疾人群体的不重视,因为它们只关注残疾特征。虽然这种反对意见在理论上不一致的基础上受到了广泛的批评,但本文强调了它在生殖遗传技术使用决策中仍然是一个重要的中介。通过借鉴 2007 年至 2009 年间在英国对患有遗传性疾病脊髓性肌萎缩症 (SMA) 的家庭和个人进行的 41 次深入定性访谈(样本为 61 人),本文强调了表达主义反对意见在 SMA 患者家庭的生殖决策中以及他们所代表的重大情感负担中如何突出体现。虽然关于表达主义反对意见的文献主要集中在那些接受产前检测的人的生殖决策上,他们对要检测的疾病几乎(或没有)事先了解,但亲密的家庭关系和对所检测疾病的广泛经验的背景从根本上改变了遗传性疾病患者家庭中表达主义反对意见的性质和影响。通过关注 SMA 患者家庭的生殖决策以及他们对表达主义反对意见的战略管理,本文将回应残疾权利支持者的呼吁,即需要向考虑选择性终止的准父母提供关于所检测残疾的“基于经验”(而不是医学)的信息。本文将论证,父母对所检测残疾的经验知识实际上可以放大对产前检测的表达主义反对意见,从而矛盾地限制而不是促进生殖决策。

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