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Human Genome Epidemiology, 2nd EditionBuilding the evidence for using genetic information to improve health and prevent disease$
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Muin Khoury, Sara Bedrosian, Marta Gwinn, Julian Higgins, John Ioannidis, and Julian Little

Print publication date: 2009

Print ISBN-13: 9780195398441

Published to Oxford Scholarship Online: May 2010

DOI: 10.1093/acprof:oso/9780195398441.001.0001

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Assessing the evidence for clinical utility in newborn screening

Assessing the evidence for clinical utility in newborn screening

Chapter:
(p.517) 26 Assessing the evidence for clinical utility in newborn screening
Source:
Human Genome Epidemiology, 2nd Edition
Author(s):

Scott D. Grosse

Publisher:
Oxford University Press
DOI:10.1093/acprof:oso/9780195398441.003.0026

This chapter outlines key methodological issues in collecting and analyzing data on outcomes in individuals with genetic disorders that are candidates for inclusion in screening panels, and reviews the relevant literature for two disorders that have relatively abundant evidence. One disorder is medium-chain acyl-CoA dehydrogenase deficiency (MCADD), which is a fatty acid oxidation disorder that is the most common of the new disorders detected by mass-throughput MS/MS technology. MCADD has been the “poster child” for expanded newborn screening. The other disorder is cystic fibrosis (CF), which is also increasingly being added to screening panels.

Keywords:   newborn screening, cystic fibrosis, genetic disorders

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