Prader-Willi syndrome is a rare genetic disease that causes poor feeding in infancy but later triggers insatiable hunger.

While receiving treatment for a car accident ten years ago, Mr Chua learnt that he had an abnormal build-up of protein in his ...

About 150 people in Singapore have transthyretin amyloid cardiomyopathy. Read more at straitstimes.com. Read more at ...

Silvana Santos' groundbreaking research uncovered Spoan syndrome, a rare genetic disorder affecting children in a remote ...

For years, families in a small Brazilian town, Serrinha dos Pintos, watched their children slowly lose the ability to walk, ...

A biologist’s decades-long research in a secluded village led to the discovery of a rare genetic condition and transformed ...

"If a couple is unrelated, the chance of having a child with a rare genetic disorder or disability is about 2–3%. For cousins ...

The challenge is not just to discover more but to ensure that our discoveries make us better—more ethical, more equitable, ...

Q1 2025 Earnings Call Transcript May 7, 2025 Geron Corporation beats earnings expectations. Reported EPS is $-0.03, ...

The mitochondrial genome can help researchers map ancestry and better understand the inheritance of mitochondrial diseases.

Immunocore reports first quarter financial results and provides a business update KIMMTRAK® (tebentafusp-tebn) net revenues of $93.9 million in Q1 2025, growing by 33% year-over-year ...