A recent breakthrough in personalized gene editing has saved the life of a baby suffering from a rare genetic disorder. The achievement marks a significant milestone in the field of CRISPR technology, which has shown promise in treating various genetic diseases. However, experts warn that the future use of this technology is uncertain due to several factors.
The high cost of gene editing services and equipment may limit accessibility to this treatment for many patients. Moreover, governments are still grappling with how to regulate the use of CRISPR technology, raising concerns about its potential misuse. Additionally, there is a shortage of skilled scientists and researchers who possess the necessary expertise to implement this technology effectively.
As the field continues to evolve, it remains to be seen whether gene editing will become a mainstream treatment option for genetic diseases. While the recent success in saving a baby’s life is a significant step forward, more research and investment are needed to overcome the current challenges and unlock the full potential of CRISPR technology.
Source: https://www.sciencenews.org/article/personalized-crispr-gene-edit-therapy