About Citrin Foundation
Citrin Foundation is a research-driven, non-profit organization set up in 2016 to tackle citrin deficiency, a monogenetic condition that is an inborn error of metabolism, as well as a secondary urea cycle disorder. Our goal is to ultimately find effective treatments and a cure for the condition. We fund research projects to better understand the condition and develop new therapies. We also provide support to citrin deficiency patients and their families globally.
For Rare Disease Day, we will be raising awareness about citrin deficiency on social media by co-creating a number of resources with our members which we will be sharing throughout the week. We have also encouraged our members to share their stories directly on the Rare Disease Day website or to be showcased in our “patient spotlight.”
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