Vanderbilt Down Syndrome Research Registry

Principal Investigator: Jeffrey L. Neul, M.D., Ph.D.


The Down Syndrome Research Registry connects families interested in research with researchers who want to better understand the challenges some individuals with Down syndrome may experience.


Child or adults with Down syndrome up to age 18.


One 60 minute appointment to complete questionnaires about demographics, health, and developmental history, and to provide a blood sample for DNA. There is no compensation for participation.


Monroe Carell Jr. Children’s Hospital at Vanderbilt

Participant Criteria

Any child or adult with Down syndrome


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Contact Information

Down Syndrome Registery Coordinator

Last Updated: Thursday, December 17, 2020

Enter your name and contact information and this study's coordinators will contact you if there are openings available.