GeneDx Blog

GeneDx offers more than a test. We’re dedicated to advancing the field of genomics—so more patients get answers.

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For Carlotta’s Family, Early Intervention Meant Everything
Rare Disease

For Carlotta’s Family, Early Intervention Meant Everything

Patient Stories
Ben’s Story: How Genome Sequencing Diagnosed Labrune Syndrome
Epilepsy

Ben’s Story: How Genome Sequencing Diagnosed Labrune Syndrome

Patient Stories
Genome Sequencing for Newborn Screening: First Results From the GUARDIAN Study
Newborn

Genome Sequencing for Newborn Screening: First Results From the GUARDIAN Study

Research & Innovation
From Dismissed to Diagnosed: A Family’s Journey to an HHT Genetic Diagnosis
Rare Disease

From Dismissed to Diagnosed: A Family’s Journey to an HHT Genetic Diagnosis

Patient Stories
Rare Disease Day: Moving Beyond Awareness to Action
Education

Rare Disease Day: Moving Beyond Awareness to Action

Education