Cystinuria Registry

What we are studying

The purpose of this research study is to create a registry of patients with cystinuria. Registries are a way of gaining new knowledge about a specific disease, especially when the disease is rare like cystinuria. Information regarding individuals with cystinuria will be collected. This will provide a better insight into the natural history of this disease and perhaps lead to the development of better treatment for those afflicted.

Who we are studying

  • Men and Women
  • Races:
    • White
    • African American
    • Asian
    • American Indian or Alaska Native
    • Native Hawaiian or Pacific Islander
    • Other
  • All Ethnicities
  • All Ages

Eligibility Criteria

  • Diagnosed with cystinuria

What is involved

  • Data will be collected from the patient's medical record
  • 1 blood sample if patient has not received genetic testing in the past

Compensation

None

Contact Information

Study Coordinator
Jessica Lange
Email
jelange@wakehealth.edu
Phone
Not Listed

Disclaimer: The information on this website is for general informational purposes only and SHOULD NOT be relied upon as a substitute for sound professional medical advice, evaluation or care from your physician or other qualified health care provider.