Jaipur: The life of 20-month-old Kartik hangs in balance. Diagnosed with spinal muscular atrophy (SMA), a rare and life-threatening neuromuscular dise.

"Everything we do is for the cause. It's a cause that's bigger than us. It's all for the kids. It's more than a football game ...

But now there is a ray of light. Lilah is scheduled for surgery on July 15 that will see a metal ring called a halo fastened ...

The use of salbutamol may improve upper limb strength and aid breathing in young children with spinal muscular atrophy, an ...

As Dr. Geary transitions out of his role, he will continue as a strategic consultant through 2026 to ensure continuity. Ionis ...

A 'fragile' girl's life has been transformed thanks to "caring and loving" staff at a hospice. Ellie, 12, from Salisbury, Wiltshire, has a rare life-limiting muscle wasting condition called Spinal ...

AbbVie, Lilly, Roche and Takeda have demonstrated strong interest in licensing innovator oligonucleotides for CNS indications ...

A girl was diagnosed with a rare muscle -wasting condition after she stopped crawling as a baby. Ellie Soares, 11, seemed ...

Newborn with SMA gene mutation receives presymptomatic treatment at SAT Hospital, a rare step in managing rare diseases.

Panelists discuss how insurance challenges impact spinal muscular atrophy (SMA) care, with prior authorizations becoming more ...

Panelists discuss how combination therapies targeting different aspects of spinal muscular atrophy (SMA), such as myostatin ...