Landmark study shows significant cost savings following exome and genome sequencing in pediatric neurological conditions
Rare Disease Day is only the beginning. Learn why early diagnosis, quality genomic data, and advocacy must work together—and how GeneDx helps drive action for rare disease.
With annual deductibles potentially met, now is a particularly good time to pursue comprehensive genetic testing.
Finally—an easy-to-understand guide to pediatric genetic testing.
Decades after an individual’s first unexplained seizure, a genetic diagnosis can still provide the clarity that they have been waiting for, and the chance for better outcomes.¹ It’s also more accessible than ever.
Seeing a spike in back-to-school concerns? AAP-recommended testing may help find answers sooner.
This NICU Awareness Month, GeneDx celebrates the healthcare heroes navigating some of the most challenging beginnings—and is here to help.
An emergency transfer put their newborn in a hospital where a genetic study was in progress. It may have changed everything.
Sarah knew something was wrong. The nosebleeds. The fatigue. The headaches. Her care team said she was fine. But her gut said otherwise.
