Cases and Conversations™: Little Voices, Big Challenges: Comprehensive Care for Pediatric Spinal Muscular Atrophy

January 9, 2025

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Overview:

Currently, there is no cure for SMA, although this may change with expanding treatment options. A rapidly changing treatment landscape is altering the clinical management of patients with SMA. Three therapies are currently FDA-approved and have dramatically impacted this condition. However, many health needs remain unmet in this patient population. As evidence of therapeutic effects continues to emerge, it is important for clinicians to be aware of evolving patient needs and strategies that can facilitate earlier diagnosis and more effective disease management. Furthermore, incorporating principles of diversity, equity, and inclusion (DEI) into SMA management is crucial to addressing disparities in healthcare outcomes among minority groups. By focusing on these areas, healthcare systems can better support the diverse needs of all SMA patients, fostering a more inclusive approach to care. Thus, this activity will feature expert discussing the assessment of bulbar function, use of novel therapies, and best practices for SMA management with a focus on minority patients.


Learning Objectives:

Upon completion of this activity, participants will be able to:

  • Apply assessment techniques to accurately evaluate bulbar function in pediatric patients with spinal muscular atrophy (SMA)
  • Analyze the latest safety and efficacy data of new disease-modifying therapies for SMA in pediatric patients
  • Formulate strategies to overcome challenges in managing patients of minority groups with SMA

Event Details

  • Event Date
    January 9, 2025
  • Event Time
    7:00 PM - 8:00 PM ET
  • Location
    Virtual
  • Target Audience
    This educational activity is directed toward pediatric neurologists, neuromuscular specialists, and neurologists. Other clinicians involved in the management of patients with SMA are invited to attend.

This activity is supported by an educational grant from Genentech, a member of the Roche Group.

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