A Northern Kentucky family is in a desperate search for answers as their 10-year-old boy battles a rare brain disorder.
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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 ...
Learn more about the gene linked to the evolutionary loss of human tails, and how, in rare cases, some people are still born ...
Scientists from UC Davis Center for Surgical Bioengineering, the MIND Institute and UC Berkeley’s Murthy Lab are developing ...
Researchers have identified specific genes containing rare mutations that significantly increase the likelihood of developing attention deficit hyperactivity disorder. These findings, published in the ...
A vanishingly rare genetic glitch in a single enzyme can erase a newborn’s brain cells in a matter of weeks, leaving doctors with almost no way to intervene. Researchers have now traced that ...
A rare form of diabetes affecting newborn babies and caused by a genetic disorder has been discovered by scientists in the UK ...
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 ...
Most patients with non-small cell lung cancer (NSCLC) that has metastasized to the brain have a dire prognosis. But Yale researchers have identified a subset of those patients with a rare genetic ...
Two of Opus's seven gene therapy assets are in clinical trials, with additional programs expected to enter the clinic.
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