🧬 CRISPR Breakthrough Editing Genes to Fight Rare Diseases

#CRISPR #GeneEditing #FutureOfMedicine #Biotech #RareDiseases #GlobalPulse #ScienceNews https://www.youtube.com/@VISIONARRAT0R

Transcript

00:00CRISPR gene editing is making headlines again. What's happening? Scientists have successfully

00:05used CRISPR to correct genetic mutations linked to rare inherited disorders in early stage

00:10clinical trials. This marks a huge leap in precision medicine. Why it matters? Instead

00:14of treating symptoms, CRISPR targets the root cause, faulty DNA. If proven safe, this could

00:17revolutionize how we treat conditions like sickle cell anemia, muscular dystrophy, and certain forms

00:21of blindness. Global impact. While the promise is enormous, ethical debates remain. Who gets

00:28access? How do we prevent misuse? And what happens if edits have unintended consequences?

00:33The breakdown CRISPR tech cuts and repairs faulty DNA clinical trials. Early success in rare disease

00:39treatment. Potential cure genetic disorders at their source. Challenges, safety, ethics, and equitable

00:46access. That's your one-minute dive into today's niche topic, CRISPR and the future of medicine.