Trial Parameters
Condition Birth Defects
Sponsor Baylor College of Medicine
Study Type INTERVENTIONAL
Phase N/A
Enrollment 200
Sex ALL
Min Age 1 Day
Max Age 18 Years
Start Date 2022-06-01
Completion 2027-01-31
All Conditions
Interventions
Whole genome sequencing (WGS)
Brief Summary
This study aims to transform the current clinical practice paradigm by leveraging an internally designed web-based model of delivery of care called Consultagene to provide remote evaluation and genomic sequencing for improving genetic health of less resourced children with rare disorders living along the Texas-Mexico border.
Eligibility Criteria
Inclusion Criteria: Pediatric patients with undiagnosed rare genetic diseases residing in the Rio Grande Valley and El Paso in Texas Exclusion Criteria: Children with known genetic diseases