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.

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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 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 (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 ...

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 ...

Living with spinal muscular atrophy. DIMITAR DILKOFF/AFP via Getty Images. By Jason Mast. March 19, 2025. General Assignment Reporter Jason Mast [email protected] ...

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.

Biohaven's spinal muscular atrophy drug fails to meet study goal. By Mariam E Sunny. November 25, 2024 7:06 PM UTC Updated November 25, 2024 Companies; Biohaven Ltd. Follow. Biogen ...