News

A new neonatal screening test recently saved the life of a little girl with spinal muscular atrophy, a rare neuromuscular ...
Abu Dhabi (DoH), the regulator of the healthcare sector in the Emirate, M42, a global health champion powered by AI, technology and genomics and PureHealth, the largest healthcare group in the Middle ...
Sheikh Mohammed bin Rashid funds Dh7 million treatment for a young Syrian girl with spinal muscular atrophy, giving her a ...
The family of Yaqeen Ibrahim Kanaker, a Syrian child, confirmed that she began treatment on Thursday at Al Jalila Children's ...
Sheikh Mohammed bin Rashid, Vice President and Ruler of Dubai, will cover Dh7 million ($1.9 million) in medical treatment for ...
The ruler of Dubai, His Highness Sheikh Mohammed bin Rashid Al Maktoum, has covered the cost of Syrian girl Yaqeen Ibrahim ...
The Syrian girl suffers from spinal muscular atrophy, a rare and serious genetic disorder that affects muscle strength and ...
Roughly 53 million people in the U.S. provide care to a family member such as a child with complex medical needs, an aging ...
Spinal Muscular Atrophy known as SMA is a rare genetic disease that affects 1 in 6,000 children. And, tonight, the parents of 6 month old baby Emiliano Flores are calling out for help for their son.
Objective The aim of this study was to assess early language acquisitions in treated individuals with spinal muscular atrophy (SMA) type 1 and in infants identified by newborn screening (NBS). Methods ...
Treatment with salanersen slowed neurodegeneration and improved motor function in children with SMA in a Phase 1 trial, ...
Biogen (BIIB) announced new data that it says reinforce the clinical impact of nusinersen across a broad spectrum of individuals affected by spinal muscular atrophy. These latest findings from Part C ...