Spinal muscular atrophy (SMA) is a rare hereditary neuromuscular disorder in which the spinal cord does not form normally.

A former Winchester University student is raising funds to help with his dream of competing in the Paralympics. Ben Morris, 24, from Swindon, is raising the funds needed to train in the sport of ...

A group of questionnaires called PROfuture can meaningfully measure a variety of symptoms of SMA that impact patients, a study reported.

As treatment for spinal muscular atrophy (SMA) has drastically improved over the last decade, so too have survival rates and the number of people with SMA living well into adulthood. | A new education ...

Upgrades to the home of a person with spinal muscular atrophy can ease daily SMA accessibility challenges and support greater ...

More Hong Kong patients suffering from spinal muscular atrophy (SMA) will be able to enjoy a government subsidy to control ...

Remini shared an emotional tribute to the 21-year-old she met while filming the "King of Queens" sitcom: "I want people to ...

The court said Switzerland’s refusal to pay for Spinraza for a quadriplegic patient with spinal muscular atrophy did not ...

For people like 16-year-old Vivienne Liedtke, who was born with the physical disability spinal muscular atrophy, finding a ...

After a season of regulatory upheaval, obesity and rare genetic diseases will likely remain major themes for biopharma in ...

It will grow to $9.02 billion in 2029 at a compound annual growth rate (CAGR) of 15.3%.” — The Business Research Company LONDON, GREATER LONDON, UNITED KINGDOM, July 3, 2025 /EINPresswire.com/ -- Save ...