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The five types of SMA are categorized by the disease's severity and the age when symptoms begin: When they think a child might have spinal muscular atrophy, doctors will order genetic testing to look ...

More research is needed to confirm gray matter, the darker tissue found in the brain and spinal cord, “as a potential disease ...

Spinal muscular atrophy (SMA) is a rare hereditary neuromuscular ... treatment and support are available to manage the symptoms and help people with SMA obtain the best possible quality of life.

Problems with chemical messengers like dopamine were tied to posture issues in SMA in a mouse study, but levodopa therapy may ease symptoms.

Is a very rare form of Spinal Muscular Atrophy caused by mutations in the gene. Symptoms appear during infancy, between ages 6 weeks and 6 months. Children with SMARD1 suddenly may be unable to ...

An investigational higher dose of spinal muscular atrophy drug nusinersen gains attention as the FDA and European Medicines ...

The five types of SMA are categorized by the disease's severity and the age when symptoms begin: When they think a child might have spinal muscular atrophy, doctors will order genetic testing to look ...

Since SMA has similar symptoms to other neuromuscular disorders, like muscular dystrophy, we’ll use diagnostic tools to rule out other conditions and determine if you have spinal muscle atrophy. Those ...

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