22/05/2025
🧬 Historic Gene Editing Breakthrough!
In a world first, doctors have successfully used CRISPR gene editing to treat a baby with a rare, life-threatening metabolic disorder—CPS1 deficiency. The treatment, delivered directly to the liver, corrected the faulty gene and helped the baby recover.
This could change the future of medicine and offer hope for those living with rare genetic diseases. 💡✨
Read the full story:
Gene-editing breakthrough has potential to treat array of devastating genetic diseases soon after birth, scientists say