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 ...

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

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, ...