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 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 ...

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

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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.

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 ...

Spinal muscular atrophy (SMA) is a progressive neurodegenerative disorder set in motion before birth. Scientists at St. Jude Children's Research Hospital led the first in utero treatment of SMA ...

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 rare genetic disorder that causes muscle weakness and disability, typically in young children. Learn about symptoms, diagnosis, treatment options, and support.

Adult-onset spinal muscular atrophy occurs over the age of 18, and commonly in a person's 30s or 40s. Learn more here.

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