RECRUITING Not applicable ClinicalTrials.gov

Genetic Inclusion by Virtual Evaluation

Sponsor: Baylor College of Medicine • ClinicalTrials.gov ID: NCT05318222

Registry updated: 2026-10-01

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Description

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.

Interventions

Whole genome sequencing (WGS) (Diagnostic test)
WGS will identify copy number variations (CNVs), single nucleotide variants (SNVs), as well as triplet repeat disorders in children with rare diseases

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

Conditions

Birth Defects Multiple Congenital Anomaly Neurodevelopmental Disorders

Locations

University of Texas Rio Grande Valley — Edinburg, Texas, United States

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Official Source

Data sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

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