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Newborn screening for lysosomal storage disorders and other neuronopathic conditions.

Authors :
Matern, Dietrich
Oglesbee, Devin
Tortorelli, Silvia
Source :
Developmental Disabilities Research Reviews; 2012, Vol. 17 Issue 3/4, p247-253, 7p, 1 Diagram, 2 Charts
Publication Year :
2012

Abstract

Newborn screening (NBS) is a public health program aimed at identifying treatable conditions in presymptomatic newborns to avoid premature mortality, morbidity, and disabilities. Currently, every newborn in the Unites States is screened for at least 29 conditions where evidence suggests that early detection is possible and beneficial. With new or improved treatment options and development of high-throughput screening tests, additional conditions have been proposed for inclusion into NBS programs. Among those are several conditions with a strong neuronopathic component. Some of these conditions have already been added to a few national and international screening programs, whereas others are undergoing pilot studies to determine the test performance metrics. Here, we review the current state of NBS for 13 lysosomal storage disorders, X-adrenoleukodystrophy, Wilson disease, and Friedreich ataxia. © 2013 Wiley Periodicals, Inc. Dev Disabil Res Rev 2013;17:247-253. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
19405510
Volume :
17
Issue :
3/4
Database :
Complementary Index
Journal :
Developmental Disabilities Research Reviews
Publication Type :
Academic Journal
Accession number :
88369030
Full Text :
https://doi.org/10.1002/ddrr.1117