On the occasion of Rare Disease Day, which was worldwide on February 28 this year, representatives of the clinical laboratory SPADIA (CEO RNDr. Martin Radina) informed about the successful ongoing collaboration with the Research Unit for Rare Diseases at the First Faculty of Medicine, Charles University in Prague, and the National Center for Medical Genomics in the field of diagnostics and research of rare genetically determined diseases (Prof. Stanislav Kmoch).
This important collaboration expands diagnostic possibilities, improves care for patients and families affected by rare diseases, and supports further research that gives patients and their families hope for accurate diagnosis, prevention, and treatment.
The link to the press release is here: https://www.spadia.cz/zdravotnici/clanky/2025/laborator-spadia-zlepsujeme-peci-o-pacienty-a-rodiny-s-vzacnymi-nemocemi