Campaigners hail ‘landmark moment’ in early detection and treatment of rare muscle-wasting disease ...

England will add SMA testing to its newborn screening program from October 2026, expanding nationwide by October 2027 to help ...

For decades, researchers studying myotonic dystrophy type 1 (DM1) have focused on the disease's underlying genetic cause: a ...

All newborns in England will now be tested for spinal muscular atrophy (SMA) in landmark change for Jesy Nelson and the ...

Niranjan, the 17-year-old Pawan Kalyan fan from Telangana battling Duchenne Muscular Dystrophy (DMD), has passed away just days after the Andhra Pradesh Deputy CM fulfilled his final wish by visiting ...

All babies in England to be screened for Spinal Muscular Atrophy National newborn screening programme for Spinal Muscular Atrophy (SMA) to be rolled ...

Jesy Nelson is sharing the moment no parent expects. And it is almost impossible to watch lightly. The former Little Mix singer breaks down in a new look at her Amazon Prime documentary as doctors ...

There is a push to reduce the demand for the plasma-derived therapy, as patients, physicians and governments worry about ...

For decades, researchers studying myotonic dystrophy type 1 (DM1) have focused on the disease's underlying genetic cause: a ...

Vor Biopharma pivots to telitacicept for autoimmune diseases, backed by $491M cash to 2029. Click here to read an analysis of ...

Years of chemotherapy marked Faye Condon’s battle against what was thought to be an autoimmune disorder, only for doctors to ...