A baby with a super rare genetic disease is now thriving thanks to a custom-made gene editing treatment. Doctors used a next-level CRISPR technique to literally fix his DNA—no liver transplant needed! This is one of the first times gene editing has been used like this, and scientists are saying it could be a game-changer for millions with rare diseases. The tech is still new, but this could be the start of something huge for personalized medicine. #GeneEditing #CRISPR #MedicalBreakthrough #RareDiseases #ScienceNews #Health