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The Crispr therapy was tailored to the baby’s specific condition and could provide a template for others.
A tailored CRISPR base-editing therapy was given for the first time to an infant who was born with a rare genetic disease, ...
The technique used on a 9½-month-old boy with a rare condition has the potential to help people with thousands of other ...
A Delaware County infant with a rare metabolic disease, CPS1 deficiency, was treated at CHOP with a custom CRISPR therapy.
The baby, KJ Muldoon of Clifton Heights, Penn., is one of 350 million people worldwide with rare diseases, most of which are ...
The goal is to reuse key parts of the treatment and simply swap in a custom set of instructions for each patient's specific ...
A range of other rare inherited diseases are now likely to be curable by similar procedures, the research team said ...
An infant with a rare urea cycle disorder became the first patient to receive a personalized gene-editing therapy. His care ...
Doctors used personal gene therapy to treat an infant with a deadly genetic disease in a medical first. KJ Muldoon was born ...
Though it may be a while before similar personalized treatments are available for others, doctors hope the technology can ...
A US baby born with a rare and life-threatening genetic disease is thriving after undergoing the first successful ...
PHILADELPHIA (WPVI) -- An infant, who was born with a deadly disease, is now thriving, thanks to a medical first performed at ...