Spinal muscular atrophy (SMA) manifests across a broad clinical spectrum, with functional status and disease trajectory varying widely among individuals. Understanding this heterogeneity is essential to anticipate progression, manage patient and caregiver burden, and optimize outcomes. Early diagnosis remains critical; newborn screening (NBS) and confirmatory genetic testing have transformed identification and management, yet real-world implementation gaps persist. Tune in to the first episode of our four-part video podcast series to hear from two leading experts as they unpack the diverse clinical presentations of SMA, examine the impact of delayed diagnosis, and discuss how early detection through NBS can reshape the course of care. Watch the full video podcast or listen on the go with the audio-only version!
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298 of a sample of 300 are free · 416 courses listed here.
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- Podcast / audio
- includes On-demand / recorded video
- Credit · Up to 0.5 credits
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ReleasedDec 30, 2025
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Last day to claim creditDec 30, 2026 3 months left
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PRIME Education, Inc. (PRIME®) Navigating the Spectrum of SMA: From Genetic Insights to Timely Diagnosis
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PRIME Education, Inc. (PRIME®) Assess, Adapt, Advance: Multidisciplinary Strategies for Long-Term Spinal Muscular Atrophy (SMA) Management
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PRIME Education, Inc. (PRIME®) Navigating the Evolving Treatment Landscape in SMA: An Interactive Clinical Decision-Making Simulation
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Medscape, LLC Meeting the Needs of Adults With Spinal Muscular Atrophy: Exploring the Prospect of Meaningful Therapeutic Gains
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MDA +1 Leveraging Genetic Testing to Optimize Early Intervention in SMA & DMD
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American Academy of Pediatrics Duchenne Muscular Dystrophy: Genetic Diagnosis, Neuromuscular, Rehabilitation, Orthopaedic and Surgical Management
