New study aims to diagnose rare diseases in newborns using virtual genetic consultations
NCT ID NCT07102966
First seen Sep 30, 2025 · Last updated May 23, 2026 · Updated 35 times
Summary
This study offers advanced genetic testing and virtual doctor consultations for seriously ill newborns in Texas hospitals with limited resources, especially near the Texas-Mexico border. Researchers will test a tool called Consultagene to see if it helps doctors diagnose rare genetic conditions faster than usual care. About 200 infants under 90 days old with suspected genetic disorders will receive rapid whole genome sequencing over 5 years.
Disclaimer
Read more
Show less
This is a summary of
the original study
.
Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for RARE DISEASES are added.
By submitting, you agree to our Terms of use
Contacts and locations
Show contact details
Enter your email to view the contact information for this study.
By submitting, you agree to our Terms of use
Study contacts
-
Contact
Phone: •••-•••-•••• Email: •••••@•••••
-
Contact
Email: •••••@•••••
Locations
-
Baylor College of Medicine
RECRUITINGHouston, Texas, 77030, United States
Contact Phone: •••-•••-•••• Email: •••••@•••••
Conditions
Explore the condition pages connected to this study.