Nearly 80% of all rare diseases have a genetic cause. For many patients, whole-genome sequencing can provide a diagnosis, which can prevent unnecessary additional testing, lead to stronger medical management, and provide a link to a community for support. But not all patients receive a definitive answer. Join experts to learn about the strengths and limitations of sequencing for rare disease.
Speakers: Shimul Chowdhury, MD, Ryan Taft

Stay Connected
Sign up for updates straight to your inbox.