Texas study aims to speed up rare disease diagnosis for newborns
NCT ID NCT07102966
First seen Sep 30, 2025 · Last updated May 13, 2026 · Updated 32 times
Summary
This study provides advanced genetic testing and virtual doctor consultations for seriously ill newborns in Texas hospitals with fewer resources, especially near the Texas-Mexico border. Researchers will test a virtual consultation tool called Consultagene and gather feedback from healthcare providers. About 200 infants under 90 days old with suspected genetic disorders will receive rapid whole genome sequencing. The goal is to see if this approach helps diagnose rare diseases faster than usual care.
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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.
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Study contacts
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Contact
Phone: •••-•••-•••• Email: •••••@•••••
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Contact
Email: •••••@•••••
Locations
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Baylor College of Medicine
RECRUITINGHouston, Texas, 77030, United States
Contact Phone: •••-•••-•••• Email: •••••@•••••
Conditions
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