Niklas Juth Knihy

"This book will interest academic researchers and professionals involved with genetics and insurance."--Jacket

This book provides an in-depth analysis of the ethical, political, and philosophical issues surrounding health-oriented screening programs. It examines the values promoted or compromised by these programs, conflicts arising in health care and public health, and offers insights relevant to health care ethics, appealing to professionals and the public alike.

The book explores the ethical implications of genetic testing for health predictions, addressing critical questions about the extent of testing and access to results. It emphasizes the importance of patient autonomy and subjective well-being in the context of presymptomatic testing. The author argues for the individual's right to decide whether to inform relatives about genetic information, while critiquing the notion that such information is communal. Additionally, the text discusses broader societal issues, including the rights of insurance companies to genetic data, advocating for a robust welfare state in light of genetic advancements.