ScreenPlus: A comprehensive, multi-disorder newborn screening program.
Ontology highlight
ABSTRACT: The increasing availability of novel therapies highlights the importance of screening newborns for rare genetic disorders so that they may benefit from early therapy, when it is most likely to be effective. Pilot newborn screening (NBS) studies are a way to gather objective evidence about the feasibility and utility of screening, the accuracy of screening assays, and the incidence of disease. They are also an optimal way to evaluate the complex ethical, legal and social implications (ELSI) that accompany NBS expansion for disorders. ScreenPlus is a consented pilot NBS program that aims to enroll over 100,000 infants across New York City. The initial ScreenPlus panel includes 14 disorders and uses an analyte-based, multi-tiered screening platform in an effort to enhance screening accuracy.
SUBMITTER: Kelly NR
PROVIDER: S-EPMC10761901 | biostudies-literature | 2024 Mar
REPOSITORIES: biostudies-literature
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