New registry of patients with achondroplasia
Achondroplasia is a rare genetic condition, which affects the normal growth of human skeleton. It is important for patients, their families and physicians to be able to connect and to share information. A new registry, entitled ReACH, has been developed in cooperation between the Faculty of Medicine of the Masaryk University (FM MU) and the Institute of Biostatistics and Analyses of the Masaryk University (IBA MU).