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Researchers say the CRISPR-based technique used could eventually be employed to treat more people with rare genetic diseases ...
Treatment seems to have been effective, but it is not clear whether such bespoke therapies can be widely applied.
A pivotal medical milestone has been reached. For the first time ever, researchers have used a personalized CRISPR-based gene ...
He’s among the first to be successfully treated with a custom therapy that seeks to fix a tiny but critical error in his ...
3don MSN
Doctors have successfully used gene-editing therapy to treat an infant born with a rare disorder. Experts believe the ...
5don MSN
A team of doctors at the Children's Hospital of Philadelphia and Penn Medicine treated a baby with a gene editing technology ...
KJ received the bespoke CRISPR treatment 6.5 months after birth, receiving three infusions of the therapy as of April 2025.
The Crispr therapy was tailored to the baby’s specific condition and could provide a template for others.
A team of doctors and scientists have successfully treated a rare genetic condition with the first-ever personalized ...
5d
New Scientist on MSNBaby with rare disease given world-first personal CRISPR gene therapyBy Michael Le PageA baby boy with a life-threatening genetic condition has become the first person to receive a bespoke ...
A personalized gene editing therapy was successfully used to treat an infant with CPS1 deficiency, a disease that causes ...
A research team has developed and safely delivered a personalized gene editing therapy to treat an infant with a life-threatening, incurable genetic disease. The infant, who was diagnosed with the ...
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