GeneDx

When a cerebral palsy diagnosis didn’t fully explain Rosie’s developmental delays, hearing loss, and complex medical history, her family kept searching for answers.

Genetic testing ultimately revealed an underlying rare condition, bringing long-awaited clarity and helping guide future care for Rosie and her family.

Read Rosie’s story to learn how genetic testing can help families and clinicians look beyond a single diagnosis when symptoms don’t fully add up.
https://genedx.co/4a7BmHP

What if answers came sooner, not just for some patients, but as a standard of care?

What if care felt truly connected across specialties, systems, and settings?

What if progress didn’t stall in silos, but moved at the speed of science?

On March 3, leaders across healthcare, research, policy, and innovation will gather at the CNBC Cures Summit to explore what’s next for precision medicine and patient care.

We’re proud that our GeneDx leaders will be part of that conversation bringing perspective from the front lines of genomic medicine and the families we serve.

Join the FREE livestream on March 3 and be part of the conversation shaping the future of care → https://www.cnbcevents.com/cures/