U.S. President Donald Trump signed a spending package into law Tuesday that reauthorizes the FDA’s previously stalled rare ...

Millions of children with rare diseases set to benefit from faster diagnosis and better treatments - A new platform is being ...

A Florida state legislator sponsored the nation's first state-backed genetic screening program after his son died from a rare genetic disease.

Congress has finally acted, but the legislation did not come soon enough for many.

Every year in the United States, thousands of families face a devastating reality: Their child has a rare disease, but they won’t know it until it’s too late for effective intervention. Thirty percent ...

Bipartisan legislation aims to give kids with cancer and other potentially terminal diseases more treatment options; Mullin ...

From rare cancers caught early to dementia foretold decades in advance, newborn genomic testing raises an unsettling question ...

Khaberni - Out of every 125 million people, only one contracts the disease known as 'CIPA' (Congenital Insensitivity to Pain with Anhidrosis), and in broader estimates for the general lack of pain ...

GeneDx (Nasdaq: WGS), the leader in rare disease diagnosis and improving health through the power of genomic data, today announced that its President and Chief Executive Officer Katherine Stueland has ...