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FDA approves 1st-ever gene therapy to restore hearing

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Overview
 · 3h · on MSN
FDA approves first gene therapy for inherited deafness, shown to restore hearing for children with rare condition
The US Food and Drug Administration on Thursday approved the first gene therapy for inherited hearing loss, a one-time treatment that proved to be life-changing for a small number of children in a clinical trial who were born without hearing.

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 · 2h
FDA approves first gene therapy for genetic hearing loss
 · 4h
New Gene Therapy Enables Children With a Rare Form of Deafness to Hear
Boise State Public Radio · 3h
The FDA gives the green light to the first gene therapy for deafness
The Food and Drug Administration approved the first gene therapy to restore hearing for people who were born deaf.

Continue reading

STAT · 1d
Gene therapy trial for deafness adds evidence to drug’s efficacy
KUOW · 1d
Gene therapy for a rare type of deafness shows lasting results
3don MSN

Redheads May Have Some Genetic Advantages. But They Are Predisposed to Other Illnesses, Scientists Say

Research into ancient DNA samples has discovered that those who carry genes for red hair also are have immune benefits — but are more likely to have celiac disease
2don MSN

Unexpected cancer mutations in brain's immune cells may help fuel Alzheimer's disease

As the body ages, cells naturally accumulate dozens of genetic mutations each year. New research from Boston Children's Hospital, published in Cell, finds that the brain's resident immune cells, microglia,
9d

A New AI Tool Could Transform How We Diagnose Genetic Diseases

Researchers say a new AI system can identify disease-causing mutations and explain their biological effects, potentially changing how genetic disorders are diagnosed.
Yahoo
11mon

Rare genetic mutation lets some people thrive on just 4 hours of shut-eye

Some lucky people have rare genetic mutations that enable them to feel well-rested after just four hours of sleep, while the rest of us need around eight hours to function. Now, researchers have identified one of these mutations, named SIK3-N783Y, in a ...
1d

Study explores the genetic basis of an encephalopathy associated with epilepsy and autism

SYNGAP1 encephalopathy is a rare genetic disorder for which there is no treatment. It causes epilepsy, intellectual disability, psychomotor delay and, frequently, autism. It arises from mutations in the SYNGAP1 gene,
News 6 WKMG
12mon

Genetic medicine can leave people with rare mutations behind. But there's new hope

This photo provided by Emilys Entourage in April 2025 shows Emily Kramer-Golinkoff, who has cystic fibrosis caused by a rare genetic mutation, during a trip to Maine. (Emilys Entourage via AP) (Uncredited, Emily’s Entourage) Emily Kramer-Golinkoff can ...
Multiple Sclerosis News Today
3h

Scientists studying yak genetics discover myelin repair mechanism

Scientists studying animals at high altitudes discovered a previously unknown mechanism that is key for regulating myelin repair.
National Geographic news
7mon

The curious case of the tigers who changed their stripes

Decades ago, India’s tigers were on the brink of extinction. Slowly, their numbers have rebounded. But that ecological success has prompted a dire problem—and a race to save many of them from genetic collapse. In 2014 just four tigers remained in India ...
Forbes
7mon

Does Smoking Cause Genetic Mutations In Your Children?

A man sits outside and holds a slim menthol cigarette between his fingers. Close-up with focus on the cigarette. The study provided a comprehensive examination of how lifestyle and environmental factors impact the rate of new genetic changes. These changes ...
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