For Clinicians
We support the RTD scientific and medical community by providing the tools necessary to execute their best work and improve patient outcomes.
We are a world-leading resource for research into the fundamental understanding of Riboflavin Transporter Deficiency (RTD), its diagnosis and treatments. If you are considering a diagnosis of RTD or want information on this disorder, we can provide you with information on symptoms and latest research findings, including access to the world´s largest reference source of published literature on RTD and topics relevant to aspects of RTD. In addition, we can connect you with other members of the medical community worldwide who have experience diagnosing and treating RTD.
Please find addition information at the links below:
Cure RTD International Registry
Human SLC52 Gene Variant Database
The Cure RTD Foundation plays a unique role as the only organization in the world with the largest cohort of individuals who have Riboflavin Transporter Deficiency (RTD), and dissemination about research and phenotype of the disorder.
In an effort to provide healthcare professionals and families with an an invaluable diagnostic tool, we continue to expand the RTD Registry to both reflect genotype/phenotype relationship and expedite updates in genetic classifications from “unknown significance”.
We need your cooperation to accomplish this goal! We would like to be in contact with you if you are a healthcare professional who has previously treated or is currently treating an individual with a genetic diagnosis of RTD. For more information about the services we provide, please contact us.
