内容摘要：The Associated Press Health and Science Department receives support from the Howard Hughes Medical Institute’s Science and Educational Media Group and the Robert Wood Johnson Foundation. The AP is solely responsible for all content.

The Associated Press Health and Science Department receives support from the Howard Hughes Medical Institute’s Science and Educational Media Group and the Robert Wood Johnson Foundation. The AP is solely responsible for all content.

Barbot worked with local rabbis, as well as doctors and nurses in the Jewish community, to send messages that encouraged vaccine uptake. Calls from Trump and Azar, who urged the public to vaccinate, helped her make the case, too.When national leaders distance themselves from that message, she said it “starts to erode the effectiveness of people who are trying to convey those messages at the local level.”

This story has been corrected to show the name of the organization is the Infectious Diseases Society of America, not the Infectious Disease Society of America, and Dr. Carlos del Rio is its past president, not its president.Associated Press writers Paul Weber in Austin, Texas, Devi Shastri in Milwaukee and Margery Beck in Omaha contributed to this report.is growing and thriving after getting an experimental

Researchers described the case in a new study, saying he’s among the first to be successfully treated with a custom therapy that seeks to fix a tiny but critical error in his genetic code that kills half of affected infants. Though it may be a while before similar personalized treatments are available for others, doctors hope the technology can someday help the millions left behind even as genetic medicine has advanced because their conditions are so rare.“This is the first step towards the use of gene editing therapies to treat a wide variety of rare genetic disorders for which there are currently no definitive medical treatments,” said Dr. Kiran Musunuru, a University of Pennsylvania gene editing expert who co-authored the study published Thursday in the New England Journal of Medicine.

The baby, KJ Muldoon of Clifton Heights, Pennsylvania, is one of 350 million people worldwide with rare diseases, most of which are genetic. He was diagnosed shortly after birth with severe CPS1 deficiency, estimated by some experts to affect around one in a million babies. Those infants lack an enzyme needed to help remove ammonia from the body, so it can build up in their blood and become toxic. A liver transplant is an option for some.

Knowing KJ’s odds, parents Kyle and Nicole Muldoon, both 34, worried they could lose him.“The one thing my mom asked was: ‘Did you get Aggie?” Carolyn recalls.

Many pet owners struggled to reach their domesticated animals during the frantic rush to evacuate from the Palisades wildfire in January.Aggie, who is about 5 years old, was gifted to Katherine Kiefer by a friend during the COVID-19 pandemic. Social media users have been so touched by the pair’s reunion video that many have been asking for daily updates. The family’s $30,000 GoFundMe campaign for Aggie’s vet bills had topped $21,000 by Tuesday afternoon.

The cat has undergone several blood transfusions and is now seeing a specialist.“She was basically skin and bone, and in a state of absolute starvation,” Carolyn said.