Do you need a genetic test, but have problems accessing it? The Discover Dysplasias® program provides individuals suspected of having an inherited skeletal dysplasia (incl. OI) access to high-quality genetic testing. Early access to testing can enable an accurate diagnosis, which can lead to improved patient outcomes.

Blueprint Genetics and BioMarin collaborate to offer a no-cost 419-gene panel for the diagnosis of the genetic cause of skeletal dysplasias (incl. OI). This program is available for individuals in certain countries in Europe and the Middle East who meet the eligibility criteria. The comprehensive testing strategy in this program offers increased potential for establishing a molecular diagnosis.

For more Information on eligibility, participation and the complete list of countries follow this link.