By physician referral or invitation only

UNC Pediatric Rare Disease Registry

This registry will collect data about pediatric patients with rare genetic diseases. This data and participating patients will enable current and future research aimed at better understanding, diagnosing, and treating patients affected by a wide range of genetic conditions.

Age & Gender

0 years ~ 17 years
Male, Female, Gender Inclusive

Contact the Team

Location

Thank you for your interest, but this study is recruiting by invitation only.

North Carolina (Statewide), South Carolina, Virginia

Additional Study Information

Principal Investigator

Arti Pandya
Pediatrics - Genetics and Metabolism

Study Type

Clinical or Medical
Registry

Study Topics

Child and Teen Health
Genetics and Genetic Disorders
Rare Diseases

IRB Number

20-2559

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Questions?

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