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The GeneDx Blog
With annual deductibles potentially met, now is a particularly good time to pursue comprehensive genetic testing.
Three hospitals. Two surgeries. One rare disease diagnosis. How a determined mom and dad fought for their newborn daughter to help her survive–and thrive.
Unexplained epilepsy doesn’t have to remain unexplained. Even for adults, answers are within reach.
Genetic testing options for children: a comprehensive guide
A useful tool for back-to-school concerns
Celebrating NICU heroes, big and small
From dismissed to diagnosed: A mom’s 4-year journey for answers—and what it meant for her son
AAP recommends exome and genome sequencing for global developmental delay and intellectual disability
When the search ends, life can move forward
What is the “Diagnostic Odyssey” And how do we end it?
How to talk to your child’s doctor about genetic testing
A breakthrough in autism research: 230 new genes now associated with autism
When a cerebral palsy diagnosis isn’t diagnosis enough: How one mom’s tenacity got her daughter exome testing—and answers
Introducing GeneDx Discover Snapshot for patient advocacy organizations
One courageous mom found the genetic cause behind her daughter’s cerebral palsy–and then found the silver lining
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
