Screening Before We Know: Radical Uncertainties in Expanded Prenatal Genetics
نویسندگان
چکیده
In this article, we discuss the radical uncertainties unleashed by expanded prenatal genetics. We show how are now routinely screening fetuses in absence of two essential sorts information. At population level, do not have sound, unbiased data about prevalence, penetrance, and clinical variability most mutations. level proband, it is often too soon to discern relevant information fetus’ phenotype. First, outline longstanding ethical objections newborn for poorly understood genetic anomalies disorders, explain limits our understanding their penetrance variability. Next, contrast strong restrictions regulations around with more laissez-faire framework screening, using rollout non-invasive testing (NIPT) as timeliest illuminating example. new conditions added NIPT kits based on technological feasibility profit motive, leading widespread incompletely disorders. Finally, explore myriad dilemmas that ‘screening before know’ creates counsellors, caregivers, prospective parents age argue an approach openly embraces face.
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ژورنال
عنوان ژورنال: OBM genetics
سال: 2021
ISSN: ['2577-5790']
DOI: https://doi.org/10.21926/obm.genet.2104140