In a groundbreaking medical achievement, US doctors have successfully used CRISPR-based gene-editing therapy to treat a baby born with a rare and life-threatening genetic condition. The therapy, tailored specifically to correct a unique mutation in the infant’s DNA, marks a major leap toward individualised treatments for rare genetic diseases. What Is CPS-1 Deficiency? Baby KJ’s … Continue reading Gene-Editing Therapy Saves Baby with Rare Genetic Disorder