Abstract
Genetic testing has revolutionised disease diagnosis, treatment, and prevention in the medical field. This study explores the rapidly developing field of genomic medicine, highlighting developments while negotiating the complex issues of genetic testing privacy and ethics. The study carefully considers the difficulties of protecting patient genetic data and suggests strategies based on awareness-raising, education, and flexible consent-processing. The all-encompassing framework aims to provide a strong ethical basis by enforcing stringent access rules, anonymising data, and guaranteeing regulatory compliance. This study promotes public awareness-building and education of healthcare providers to create a climate in which people actively engage in decisions about their genetic information. Besides, it adds to the conversation about responsible and ethical practices in genomic medicine, protecting patient privacy and advancing the field towards a future of compassionate and knowledgeable healthcare by highlighting the dynamic nature of consent and the constant need for careful monitoring.
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