Virginia Tech researchers discovered an indication hidden in the brain that may help doctors identify children suffering from ...
Researchers have identified specific genes containing rare mutations that significantly increase the likelihood of developing attention deficit hyperactivity disorder. These findings, published in the ...
Experiments on an ultra-rare genetic mutation that causes neurodegeneration in children have helped uncover a new mechanism by which brain cells die. A team led by scientists at the German research ...
A study suggests overactive VCP may contribute to ALS nerve damage by disrupting nuclear pore proteins in genetic ALS.
Is Obesity Genetic or Environmental? Get All the Details This article was reviewed by Lynn Marie Morski, MD, JD. Key ...
Opus Genetics launches gene therapy clinical trial for MERTK-related retinitis pigmentosa: Research Triangle Park, North Carolina Wednesday, January 28, 2026, 16:00 Hrs [IST] Opus ...
News Medical on MSN
First topical CRISPR gene therapy corrects disease-causing mutations in human skin
Gene-editing tools like CRISPR have unlocked new treatments for previously uncurable diseases. Now, researchers at the ...
Two of Opus's seven gene therapy assets are in clinical trials, with additional programs expected to enter the clinic.
Kaitlyn and Gerard Norton welcomed their daughter, Madeline, into the world. Six months later, the family found itself in a unique situation, regularly traveling to another state for medical care and ...
Decluttering Mom on MSN
3-year-old girl faces second organ transplant after rare genetic condition affects both her and her brother
In a small corner of Northern Ireland, a three year old girl is gearing up for her second major organ transplant before she ...
BEAVERTON, Ore. (KOIN) – Just 21 months ago, Tommy and Linda Pham welcomed their son Raiden into this world. But when he was 3 months old, they noticed something was wrong. “He wasn’t hitting ...
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