The story of sickle cell disease in Michigan has always been one of resilience. Black families have advocated, organized, and cared for each other when systems looked the other way. This program has ...

Despite making significant clinical progress, CRISPR Therapeutics (NASDAQ: CRSP) has been struggling financially in the past ...

Experts make case for early testing, prevention and care In this report, VINCENT KURAUN explores the groundbreaking ...

Health camp certifies 35 sickle cell patients for disability benefits, emphasizing prevention, early detection, and community support.

Doctors announced this week that they have treated a newborn baby with a rare genetic disease using the world’s first personalized gene editing therapy. Geoff Bennett discussed the treatment and its ...

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

A 30-year-old mother is demanding change through a petition after suffering with one of the most common genetic disorders all ...

A team of doctors and scientists have successfully treated a rare genetic condition with the first-ever personalized ...

G ene therapy has always held enormous promise to correct genetic diseases, but turning that potential into treatments has ...