Screening for C3 deficiency in newborns using microarrays

23Citations
Citations of this article
24Readers
Mendeley users who have this article in their library.

Abstract

Background: Dried blood spot samples (DBSS) from newborns are widely used in neonatal screening for selected metabolic diseases and diagnostic possibilities for additional disorders are continuously being evaluated. Primary immunodeficiency disorders comprise a group of more than one hundred diseases, several of which are fatal early in life. Yet, a majority of the patients are not diagnosed due to lack of high-throughput screening methods. Methodology/Principal Findings: We have previously developed a system using reverse phase protein microarrays for analysis of IgA levels in serum samples. In this study, we extended the applicability of the method to include determination of complement component C3 levels in eluates from DBSS collected at birth. Normal levels of C3 were readily detected in 269 DBSS from healthy newborns, while no C3 was detected in sera and DBSS from C3 deficient patients. Conclusions/Significance: The findings suggest that patients with deficiencies of specific serum proteins can be identified by analysis of DBSS using reverse phase protein microarrays. © 2009 Janzi et al.

Cite

CITATION STYLE

APA

Janzi, M., Sjöberg, R., Wan, J., Fischler, B., von Döbeln, U., Isaac, L., … Hammartström, L. (2009). Screening for C3 deficiency in newborns using microarrays. PLoS ONE, 4(4). https://doi.org/10.1371/journal.pone.0005321

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free