While the medical world is melting down from the absolute apocalypse that is RFK Jr., it's good to celebrate that (at least ...

Sickle cell disease is a devasting disorder that affects approximately 100,000 people in the U.S., leading to anemia, severe pain, stroke and even early death. Receiving orphan drug designation from ...

The personalized CRISPR treatment could be the future of gene therapy, but hurdles remain before everyone has access.

In medical breakthrough, a baby diagnosed with rare genetic disorder is thriving after customized CRISPR gene editing therapy ...

KJ Muldoon came into the world with a genetic time bomb ticking inside him.

Over the past few years, investors have moved away from somewhat speculative and unprofitable companies to put their money ...

A team of researchers at Columbia, Harvard and University of Minnesota has developed a gene editing technique they say could ...

Innovations in gene editing, expanding global diagnostic infrastructure, and strong government initiatives are driving the hemoglobinopathies market's projected 11.56% CAGR through 2032, according to ...

The child will need to be monitored throughout his life, but researchers said the treatment’s success indicates that other ...