Democratizing precision neurology:
Expanding first-line genome access for every child in need
Date: Tuesday, November 17, 2026
Time: 12:00 PM ET | 9:00 AM PT
Webinar duration: 60 minutes
Registrants will receive a recording of the webinar approximately one week after the event.
In child neurology, defining an underlying genetic etiology is often stalled by fragmented approaches to testing, including tiered, single-gene, or panel testing. A broad “genome-first” model has the potential to simplify clinical workflows by replacing multiple diagnostic steps with a single, highly comprehensive test—helping clinicians reach diagnostic clarity sooner for children with complex neurodevelopmental disorders, refractory epilepsies, or unexplained tone anomalies.
During this session, our speakers will:
- Examine the clinical justification for adopting broad genomic sequencing as an initial diagnostic tool
- Explore which patient phenotypes may benefit most
- Discuss the importance of expanding access to testing to help reduce diagnostic disparities
- Demonstrate how a “one-test” strategy can provide clinicians with insights to guide personalized management earlier in a child’s care journey