Symptoms of SMA type 2 can be moderate or severe. Usually, children with this type of the disease can sit without help, but they do need help walking.

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 ...

Though rare, adults can get spinal muscular atrophy. When SMA symptoms begin in adulthood, ... When this protein is missing, the neurons die off, leading to the symptoms of the disease.

Spinal muscular atrophy (SMA) is a rare genetic disorder that causes muscle weakness and disability, typically in young children. Learn about symptoms, diagnosis, treatment options, and support.

Muscle weakness could be a sign of spinal muscular atrophy, ... More than 25,000 Americans have the disease. SMA is the No ... There are FDA-approved treatments for SMA that can ease symptoms and ...

Spinal muscular atrophy type 1 is the most common form of the condition, ... juvenile or adult onset SMA, or Kugelberg-Welander disease. Symptoms usually develop sometime between 18 months of age ...

Hyderabad: Spinal muscular atrophy (SMA) is a genetic disease affecting the central nervous system, peripheral nervous system, and voluntary muscle movement (skeletal muscle). August is observed as ...

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 ...

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 ...

Children suffering from Spinal Muscular Atrophy (SMA) – a rare but debilitating genetic condition – are being denied a simple ...