Back to All Events

Advisory Committee on Heritable Disorders in Newborns and Children

The committee heard from experts in the field and discuss issues related to newborn screening information, education, training activities, and training resources. The committee also heard presentations on the use of genomic sequencing in newborn screening as well as the clinical setting for both well and sick infants. In addition, the committee discussed the nomination of cerebrotendinous xanthomatosis (CTX) to the RUSP