Doctors have been able to uncover what causes SMA. They now classify types of the disease. Which one you have depends on when symptoms start and how critical they are. Usually, the earlier SMA ...

Rosero S, Weinstein MS, Seabury J, et al. Disease burden in children with spinal muscular atrophy: results from a large cross-sectional study. J Child Neurol . Published online December 19, 2022 ...

In the first part of this series, we explored how early genetic screening and gene therapy transform the lives of newborns ...

Hyderabad: Spinal muscular atrophy (SMA) is a genetic disease affecting the central ... Recognizing the early signs and symptoms of Spinal Muscular Atrophy (SMA) in infants is crucial for timely ...

MRI imaging scans can track muscle changes in SMA children given Spinraza, a study found, with better results seen with early ...

Spinraza (nusinersen) treatment helped school-age children with SMA be more independent in tasks involving their arms and ...

Spinal muscular atrophy (SMA) is a severe neurological disease for which there is presently no cure, although current therapies can alleviate symptoms. In the search for better treatment options ...

To address the condition effectively, it is crucial to focus on addressing its symptoms through a multidisciplinary ... and the public about rare diseases and SMA so that they’re able to ...

What Is Spinal Muscular Atrophy? Spinal muscular atrophy (SMA) most often affects babies and children and makes it hard for them to use their muscles. When your child has SMA, there's a breakdown ...

Spinal muscular atrophy (SMA) is a rare genetic disorder that causes severe muscle weakness. SMA usually affects children, and is typically diagnosed in the first 18 months of life. In its most ...

Spinal muscular atrophy (SMA) is a severe neurological disease for which there is presently no cure, although current therapies can alleviate symptoms. In the search for better treatment options ...