2018 NBSTRN Network Meeting Presentations

Thank you to all for attending and participating in the 2018 NBSTRN Network Meeting, held July 31- August 1, 2018 in Bethesda, MD.  The one and half day meeting showcased the use of genomic sequencing in newborns, discovering novel technologies to screen and diagnose newborns, expanded treatment options for NBS conditions, and creative collaborations between the NBS system and industry.  We hope you found the meeting to be informative and worthwhile.

Below you will find presentations from the speakers at the 2018 NBSTRN Network Meeting:

NBSTRN Update- Michael Watson

The BabySeq Project: A Study of Newborn Genomic Sequencing- Ingrid Holm

Newborn Screening Implementation Pilots: Statistical Considerations on the Path to Nationwide Newborn Screening- Amy Brower

The “Epidemic” of Prenatal Diagnoses of Sex Chromosome Aneuploidy and the eXtraordinarY Babies Study- Nicole Tartaglia

Newborn Infant Vision Test- Angela Brown

Metabolites Measured by Newborn Screening and Risk of Wheezing in Early Childhood?- Kelli Ryckman

Enhancement Newborn Screening to Improve the Efficacy of Cord Blood Transplant for Krabbe Disease- Thomas Langan

Ten Years of Newborn Screening for Severe Combined Immunodeficiency- Jennifer Puck

Urea Cycle Disorders - Newborn Screening Candidates- Susan Berry


Published On: 
Tuesday, September 4, 2018