WASHINGTON – The Food and Drug Administration published draft guidance on Tuesday that would streamline approvals of some ...
A case report documents rapid progression and death in a lung cancer patient with a rare EGFR PACC mutation who showed ...
Therapy pioneered by biotechnology Chinese firm HuidaGene showed promise in animals but caused a fatal reaction in a child.
By studying hypertrichosis, a rare condition that causes excessive hair growth, researchers uncovered signals that tell hair ...
A study of 3.37 million people of European ancestry associated the rare inherited EGFR T790M variant with about 25 times the ...
A genetic study of nearly 4,000 people with OCD or tic disorders identified 36 genes in which rare damaging mutations sharply raise the odds of these conditions. Most of the genes appear to be shared ...
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Seoul St. Mary's Hospital confirms gene-editing potential for rare kidney disease Gitelman syndrome
South Korean researchers have successfully corrected a genetic defect underlying Gitelman syndrome, a rare hereditary kidney ...
A recent case report highlights a child with primary erythromelalgia driven by a novel SCN9A gene mutation who achieved ...
A Birmingham baby started chemotherapy at just one month old after being diagnosed with a rare eye cancer following a newborn genetic study.
A rare genetic change may help explain why some people with a high-risk Alzheimer’s gene remain mentally sharp into old age.
An NIH grant will help Austin musician Casey McPherson advance testing of a treatment developed for his daughter’s rare ...
Doctors gave him until age 5. Now 13, Jaxson plays three sports — and his family's push for a cure is halfway to the next ...
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