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

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.

Spinal muscular atrophy (SMA) is a group of disorders that causes muscle weakness and wasting. SMA affects approximately, 1 in every 6,000 to 10,000 people. Adult-onset SMA usually happens ...

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Spinal Muscular Atrophy, or SMA, was once the leading cause of genetic deaths in infants. Early screenings and targeted therapies have changed that. IE 11 is not supported.

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 ...

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 genetic condition that every parent should be aware of, as it can significantly impact a ...

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 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.