Tragedy strikes as an Arizona resident dies from pneumonic plague, marking the first death in Coconino County since 2007. Health officials stress the risk to the public remains low, urging awareness and prevention measures.
An 8-year-old boy's life took a dramatic turn as he regained mobility through an experimental treatment for a rare genetic disorder. After months of decline, hope emerged with a pioneering drug that bypasses the genetic mutation.
In an unprecedented medical achievement, a child with a rare genetic disorder receives a customized CRISPR gene therapy, paving the way for future treatments of similar conditions.
In a groundbreaking case, a 6-month-old baby boy named KJ was treated with a personalized CRISPR gene-editing therapy, correcting a dangerous mutation before it could threaten his life. This innovative approach promises hope for similar cases.
KJ Muldoon, born with a deadly genetic disorder, received a groundbreaking CRISPR treatment just six months after birth. His remarkable progress showcases the future of personalized medicine for rare diseases.
The final autopsy results of Gene Hackman and his wife, Betsy Arakawa, reveal shocking health conditions and the tragic circumstances surrounding their deaths, including hantavirus and advanced Alzheimer's.
Emily Kramer-Golinkoff, a cystic fibrosis patient with a rare mutation, highlights the struggles of those left behind as gene therapies show promise for others. Her journey underscores the need for equitable treatments in rare genetic conditions.
The world mourns the loss of Prince Frederik of Luxembourg, who passed away at just 22 due to a rare genetic condition. His father, Prince Robert, shares a heartfelt tribute highlighting Frederik's inspiring legacy and dedication to finding a cure.
