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What is Riboflavin Transporter Deficiency? Welcome to the Cure RTD (formerly BVVL) website. We are the first UK website set up specifically to provide information, offer support and consolidate information on Riboflavin Transporter Deficiency. If you are visiting this site, then you or a loved one may already be affected by this rare syndrome. We hope to offer you support and some answers to your questions. Perhaps you have a SWAN (syndrome without a name) child and are striving for a diagnosis?

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BVVL International was founded as an aid to anyone interested in uncovering the mystery of Brown-Vialetto-Van Laere syndrome and ultimately,. In finding a cure. On March 4th, 2010, the first article outlining a BVVL gene. Was published. Since that time, other genes have been discovered that elucidate this disease as a riboflavin transporter gene mutation. See the BVVL Research Highlights. Page for more information. On November 26th, 2010, an article outlining a potential therapy. Page for more information.

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