A RECOMMENDATION for the HSE not to cover the cost of a drug to help children with a rare muscular disease has been blasted by families. Last year, The Irish Sun highlighted the plight of ...

Researchers at the University of Basel have developed a gene therapy that could potentially treat a rare and currently fatal ...

Researchers developed a gene therapy for LAMA2-related muscular dystrophy that restored muscle and nerve function in mice.

In Trumbull County, a local nonprofit will once again be hiding colorful candy-filled eggs in yards this Easter to help a ...

Kochi: The state govt has spent Rs 1,600 crore to provide free medical treatment to the public, health minister Veena George said on Tuesday. She was .

The Pro-Human Declaration was finalized before last week's Pentagon-Anthropic standoff, but the collision of the two events wasn’t lost on anyone involved.

Solid Biosciences Inc. (Nasdaq: SLDB), a life sciences company developing precision genetic medicines for neuromuscular and cardiac diseases, today announced presentations on SGT-003, its ...

With parental consent, 14-year-old Praise Adams speaks to TEMITOPE ADETUNJI about living with a disability caused by muscular dystrophy, a condition that began affecting her in early childhood, her ...

Following a debunked fake image, The Mandalorian and Grogu unveils our best look yet at Rotta the Hutt ...

The first signs of distress appeared when Punarvika was just five months old. She was unable to hold her neck upright, struggled to move her legs and failed to gain weight like other children her age.

Early diagnosis of rare diseases in children can significantly improve treatment outcomes and quality of life. Learn symptoms, challenges, and why early detection is crucial for managing pediatric ...

The model of the charity allows children with life-limiting conditions to receive care in the comfort of their own homes, avoiding stressful hospital trips and helping families create special memories ...