What is it about?

Science and society have never been as dependent on each other as they are today. We must also learn from the past episodes of eugenics and we need to investigate fraudulent practices and cases of failure in scientific research that have often occurred due to merciless scientific competition, profit-seeking commercial interests, or individual pride. Genome editing raises numerous legal questions, such as: Would it be possible to make a legal difference between specific versions of gene editing? Who decides on what is considered a disease or an anomaly, a condition, or a variation? Which diseases are worth being corrected or treated and which ones are not? What kinds of social implications will gene editing bring about when it becomes widely available? Some normative distinctions have already been made in the case of gene therapy: separating somatic from germ-line interventions. But this distinction has not yet been analyzed in the light of the most recent editing practices.

Featured Image

Why is it important?

Genome editing also realigns the structure of ethical debates. It makes us rethink the concept of discrimination and scrutinize its cases in the field of assisted reproductive procedures. It revolutionizes the concept of medical treatment. It may increase or reduce inequalities based on health conditions. It may lead to numerous new rights in the field of genetics. Good genome editing practice can only be achieved through the close cooperation between the natural and social sciences. The present paper will endeavor to examine this new form of dialogue.

Perspectives

The Article examines how ethical norms have developed by looking at the history of how gene technologies were perceived and envisages the future of the ethical norms on genome editing.

Judit Sandor
Central European University

Read the Original

This page is a summary of: Genome Editing: Learning from Its Past and Envisioning Its Future, European Journal of Health Law, April 2022, Brill,
DOI: 10.1163/15718093-bja10081.
You can read the full text:

Read

Contributors

The following have contributed to this page