What is the purpose of this study?

The purpose of this study is to screen for Fragile X. Fragile X is NOT included in your baby's routine newborn screening. Being in this study means that your baby will have an extra test that is not part of the state newborn screening program. We hope to learn more about the benefits and problems in newborn screening for Fragile X from the families who participate in this study. We also want to learn more about how families respond and adapt when their newborn is identified with a change in the gene.

Please note, the Fragile X screening in this study is experimental, and it is not a diagnostic test. We cannot guarantee that the screening test will find all cases of Fragile X. The study is not intended to find other genetic causes of disability, developmental delay, or medical problems.

View a copy of the consent form, which includes details about the benefits and risks of participation in this study.