Jazmine Jackson and Eric Estrada, deeply devoted Eagles fans, welcomed their daughter in April 2025 and named her Sirianni, ...

Last July, when Jazmine Jackson learned she was pregnant, she and her older sister, Tyquanique, came up with a joke. They were talking about baby names, and Tyquanique said that if she ever had ...

The U.S. baby clothing market is thriving, with parents spending billions annually on stylish, safe, and comfortable apparel for their children. For retailers and e-commerce entrepreneurs, partnering ...

Wetzel and his girlfriend Bailey Fisher welcomed their first child together, a baby girl, on May 23. See the first photos of ...

Chiefs quarterback Patrick Mahomes and his wife, Brittany Mahomes, turn his charity golf tournament into a family affair.

In a medical first, a 9½-month-old baby named KJ has become the first person to receive a custom-made gene-editing treatment designed specifically to fix his rare genetic mutation. Diagnosed at ...

A nine-month-old baby has become the first person ever to be successfully treated with personalized gene editing therapy. Researchers corrected a specific gene mutation in baby KJ Muldoon‘s ...

FRIDAY, May 16, 2025 (HealthDay News) — A baby born with a rare and deadly genetic ... partly funded by the National Institutes of Health, shows that custom therapies may not be as costly ...

DR. KIRAN MUSUNURU, a gene-editing researcher at the University of Pennsylvania, who in months helped develop a targeted treatment to heal an uncommon genetic disease in a baby, a process that ...

An infant in Philadelphia has been successfully treated with a customized Crispr gene-editing therapy for a rare and deadly disease, doctors reported Thursday—a breakthrough in the futuristic ...

With doctors believing they only had six months to come up with a solution, KJ became the first patient in the world to receive a custom gene-editing drug in February — and he is thriving after ...

But a team at the Children’s Hospital of Philadelphia and Penn Medicine was able to bypass the standard years-long drug development timeline and use Cripsr to create a personalized medicine for ...