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More research is needed to confirm gray matter, the darker tissue found in the brain and spinal cord, “as a potential disease ...
Problems with chemical messengers like dopamine were tied to posture issues in SMA in a mouse study, but levodopa therapy may ease symptoms.
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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.
The mutation that causes Spinal Muscular Atrophy (SMA) can be detected in ... rather than waiting until symptoms manifest and a diagnosis is made. Opponents argue that there is not enough benefit ...
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 ...
Sidra Medicine, a member of Qatar Foundation, has established a gene therapy centre to treat rare genetic diseases such as ...
An investigational higher dose of spinal muscular atrophy drug nusinersen gains attention as the FDA and European Medicines ...