Spinal muscular atrophy (SMA) is a genetic condition in which neurons in the brain degenerate due to mutations in the survival motor neuron 1 (SMN1) gene.

Panelists discuss how spinal muscular atrophy is an autosomal recessive genetic disease affecting motor neurons with 3 ...

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Biogen said that new data examining of its already approved spinal muscular atrophy treatment Spinraza (nusinersen) indicates ...

Spinal muscular atrophy is usually diagnosed with a simple blood test. If genetic testing isn’t able to confirm SMA, there are other ways to see if your child has this disease that makes muscles ...

Maximum mouth opening, which is lower in children with spinal muscular atrophy compared to healthy kids, can be accurately measured during the first 2 years of life. Here’s why that matters.

Source Reference: Finkel RS, et al "Risdiplam for prenatal therapy of spinal muscular atrophy" N Engl J Med 2025; DOI: 10.1056/NEJMc2300802.

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.

Learn what you need to do to have a fun, safe, and stress-free day at an amusement park when you have spinal muscular atrophy.

Spinal Muscular Atrophy (SMA) is a genetic condition that every parent should be aware of, as it can significantly impact a ...

Spinal muscular atrophy is a debilitating genetic condition that’s usually fatal by a few years of age. But an intriguing case study might demonstrate a simple new treatment, with a child ...

Spinal muscular atrophy (SMA) is a genetic disorder that affects the nerves controlling muscle movement, leading to muscle weakness and loss over time. It is caused by changes in a gene called ...