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Spinal Muscular Atrophy Type 1 (SMA1) is a severe genetic disease characterized by motor neuron degeneration. While gene replacement therapy (e.g., AVXS-101/Onasemnogene Abeparvovec) has transformed the treatment landscape, motor development remains suboptimal for some symptomatic patients. This research identifies the median CMAP amplitude : Explain the concept of "narrative echo"—how repeating