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• W2110248103 abstract "This article examines the specific ways in which the gene, the clinic, and the family interact in clinical consultations over children with suspected congenital problems. It draws upon an ethnography of dysmorphology, 2 I gratefully acknowledge all the families, my collaborators (Paul Atkinson, Angus Clarke, Katie Featherstone, Daniela T. Pilz, and Maggie Gregory), the Wellcome Trust (award no. 057181/Z/99), and the Economic and Social Research Council (award no. R000239863) for their support for the studies upon which this article is based. a specialty in genetic medicine that involves the study of abnormal human forms and the description of complex syndromes. Dysmorphologists describe what they do as “genetic counselling,” a twin process of differential diagnosis and the calculation of risk of recurrence in other pregnancies. Policy treats genetic counselling as a positive knowledge practice that provides parents with information about “what is” in order that they can make informed, yet autonomous, decisions. Specifically, it is portrayed as non-interventionist. In dysmorphology the categorization of the genetic emerges as a field of uncertainty and “a new frontier.” Parents are not simply informed about “what is”; rather, the clinic engages them in the epistemological work of objectification. This work defines the abnormal alongside the clinician's performance of deferral. Participation in this motility of clinical work moves parents between definition and deferral to excite consciousness of the riskiness of reproduction, to elicit moments of reflexivity, and to accomplish shifts in perspective." @default.
• W2110248103 created "2016-06-24" @default.
• W2110248103 creator A5041589290 @default.
• W2110248103 date "2007-04-26" @default.
• W2110248103 modified "2023-09-26" @default.
• W2110248103 title "Diagnosis, Dysmorphology, and the Family: Knowledge, Motility, Choice¹" @default.
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• W2110248103 doi "https://doi.org/10.1080/01459740601183697" @default.
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