A genetics startup founded by scientists Tobias Wolfram and Alex Strudwick Young has left stealth mode, with Futurism ...

Computer geeks are dishing out up to $50,000, not on luxury cars or mega-mansions – but on a screening of their embryos to ...

Later pregnancies carry higher risks. Advances in genetic reproductive medicine, like IVF and NIPT, are making it possible ...

Gabrielius Misurenkovas can finally play football with his friends after being diagnosed with a rare genetic condition as a ...

A U.S. baby has set a world record — born from an embryo frozen for 30 years. Here’s how it happened and what it means for ...

This Baby’s One-in-a-Million Genetic Disorder Had No Cure. So Scientists Designed One Just for Him© ZME Science Kyle Muldoon plays with his son KJ after an infusion treatment.

Doctors used personal gene therapy to treat an infant with a deadly genetic disease in a medical first. KJ Muldoon was born in August 2024, and DNA sequencing revealed he had inherited two gene ...

KJ Muldoon, a 10-month-old baby, was diagnosed with the genetic disease carbamoyl-phosphate synthetase 1 deficiency after he was born. He got out of hospital on Tuesday.

A mom in Michigan credits her baby with saving her life during pregnancy, when she was diagnosed with a rare genetic condition that led to a life-threatening blood vessel problem. Amanda Banic, 35 ...

The baby, KJ Muldoon of Clifton Heights, Pa., is one of 350 million people worldwide with rare diseases, most of which are genetic.

A Californian baby was diagnosed shortly after birth with CPS1 deficiency—a rare, life-threatening metabolic disorder. This case became the world's first personalized CRISPR gene-editing therapy ...