Untangling the Promises of Human Genome Editing

Author:

Drabiak Katherine

Abstract

This article traces the rapid progression of policy pertaining to human genome germline modifications using genome editing. It provides an overview of how one fertility physician implemented and advertised experimental techniques as part of his fertility clinic services, examines US law and policy, and assesses the impact of rhetoric influencing global policy and interpretation of the law. This article provides an in-depth examination of the medical rationale driving the acceptance of genome editing human embryos in two contexts: to cure disease and treat infertility. It describes complexities in genomics and outlines risks currently associated with genome editing, asserting the available evidence fails to demonstrate genome editing constitutes a curative therapy.

Publisher

Cambridge University Press (CUP)

Subject

Health Policy,General Medicine,Issues, ethics and legal aspects

Reference238 articles.

1. 59. 21 CFR § 1271.3(d) (2017); Grant, supra note 43, at 615, 624-625; NAS MRT Report, supra note 11, at 25-38, 99-100.

2. 2. Califf, R. and Nalubola, R. , “FDA's Science-based Approach to Genome Editing Products,” FDA, January 18, 2017, available at (last visited November 16, 2018).

3. 185. Id.

4. 15. Drabiak, K. , “Engineering Consensus in the Development of Genome Editing Policy,” Hasting Center Bioethics Forum, March 14, 2017, available at (last visited November 16, 2018).

5. 128. Knoepfler, supra note 36.

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