The GeneDx Blog
Ashley refused to accept a broad cerebral palsy diagnosis and pushed for a precise genetic diagnosis for her daughter—preventing permanent nerve damage and vision loss.
One courageous mom found the genetic cause behind her daughter’s cerebral palsy–and then found the silver lining.
Introducing GeneDx Discover Snapshot for patient advocacy organizations
A rare disease diagnosis from the start: One family’s experience with genome-based newborn screening
Answers for Bodhi: After two years of searching, an exome test identified his rare condition
Like many children with a rare condition, Simon’s health problems were initially thought to be flukes
Rare Disease Month spotlight: The top five psychological benefits of a genetic diagnosis
What can a genetic diagnosis do for a child with epilepsy?
Are critically ill babies put on an unnecessary diagnostic odyssey because of conventional medical protocols? A new study says yes.
Racial disparities in genetic testing: The problem may not be what you think
Just how much of a difference does it make to order exome sequencing first?
A genetic condition may be hiding behind epilepsy
A diagnosis even before symptoms begin: First results from the groundbreaking GUARDIAN study
One mom’s seven-year journey to find answers for her son’s illness.
For Carlotta’s family, early intervention meant everything.
Scientific showcase at ASHG 2024
