Assessment of Fine Motor Abilities Among Children with Spinal Muscular Atrophy Treated with Nusinersen Using a New Touchscreen Application: A Pilot Study
Inbal Klemm, Alexandra Danial-Saad, Alexis R. Karlin, Rya Nassar-Yassien, Iuliana Eshel, Hagit Levine, Tamar Steinberg, Sharon Aharoni

TL;DR
A new touchscreen tool shows promise in measuring fine motor improvements in children with spinal muscular atrophy treated with nusinersen.
Contribution
Introduces a novel touchscreen-based assessment for detecting fine motor changes in SMA patients receiving therapy.
Findings
TATOO detected significant improvements in hand grip strength and fine motor performance.
Touchscreen metrics revealed enhancements in accuracy and speed across tasks.
RULM results were not statistically significant for SMA type 3 patients.
Abstract
Background/Objectives: Spinal Muscular Atrophy (SMA) is a genetic neurodegenerative disease characterized by severe muscle weakness and atrophy. Advances in disease-modifying therapies have dramatically changed the natural history of SMA and the outcome measures that are used to assess the clinical response to therapy. Standard assessment methods for SMA are limited in their ability to detect minor changes in fine motor abilities and in patients’ daily functions. The aim of this pilot study was to evaluate the feasibility and preliminary use of the Touchscreen-Assessment Tool (TATOO) alongside standardized tools to detect changes in upper extremity motor function among individuals with SMA receiving nusinersen therapy. Methods: Thirteen individuals with genetically-confirmed SMA, aged 6–23 years, eight with SMA type 2, and five with SMA type 3, participated. The patients continued the…
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Taxonomy
TopicsNeurogenetic and Muscular Disorders Research · Congenital Anomalies and Fetal Surgery
