Resources

There are a number of patient organizations and advocacy groups that offer resources and support for those living with cystinuria. These organizations can help you connect with other patients and can provide up-to-date information on treatments and research. Please contact an organization directly if you have questions about the information or resources it provides:

National Kidney Foundation
International Cystinuria Foundation
NephCure
GARD (Genetic and Rare Diseases Information Center)
National Organization for Rare Disorders
MyCare SolutionsTM

For additional support or information about Tiopronin Delayed-Release Tablets

ARE YOU A HEALTHCARE PROFESSIONAL?

The information in the following section is intended for US Healthcare Professionals only.