Though it may be a while before similar personalized treatments are available for others, doctors hope the technology can ...

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The baby, KJ, was born with severe CPS1 deficiency, a rare genetic condition that affects only one in 1.3 million people.

The goal is to reuse key parts of the treatment and simply swap in a custom set of instructions for each patient's specific ...

Doctors applied a personalized treatment to cure a baby’s genetic disorder, opening the door to similar therapies for others.

PHILADELPHIA (WPVI) -- An infant, who was born with a deadly disease, is now thriving, thanks to a medical first performed at ...

An Indian-origin cardiologist, Kiran Musunuru, played a key role in a groundbreaking medical milestone, helping treat a ...

The boy was born with a very rare condition called CPS1 deficiency, which is found in about 1 in 1.3 million people.

Scientists successfully used personalised CRISPR technology to ease symptoms in a baby with a rare liver disorder. This ...

The baby, now 9½ months old, received an infusion made just for him to fix his precise mutation. Read more at ...