Efficacy of Nusinersen Treatment in Type 1, 2, and 3 Spinal Muscular Atrophy: Real-World Data from a Single-Center Study

Background: Spinal muscular atrophy (SMA) is an inherited neuromuscular disease characterized by progressive muscle weakness and atrophy due to the absence of the survival motor neuron 1 (<i>SMN1</i>) gene. SMA is classified into types 0 through 4 based on the age of symptom onset and th...

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Bibliographic Details
Main Authors: Anna Lemska, Piotr Ruminski, Jakub Szymarek, Sylwia Studzinska, Maria Mazurkiewicz-Beldzinska
Format: Article
Language:English
Published: MDPI AG 2024-10-01
Series:Neurology International
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Online Access:https://www.mdpi.com/2035-8377/16/6/96
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