| Literature DB >> 28031434 |
Alda Saldan1, Gabriella Forner1, Carlo Mengoli1, Nadia Gussetti2, Giorgio Palù1, Davide Abate3.
Abstract
Congenital cytomegalovirus (CMV) infection represents a relevant cause of deafness and neurological damage in newborns. Intrauterine CMV transmission might result after primary or nonprimary infections, though at different rates (30% versus 0.2%, respectively). At present, a prenatal diagnosis of CMV infection is based mainly on maternal serology, the detection of CMV-DNA in amniotic fluid and fetal blood, and ultrasound (US) and magnetic resonance imaging (MRI). Recent evidences suggest that congenital CMV infection may be an immune-mediated disease and that evaluation of humoral and especially T-cell immunities may improve the overall prenatal diagnosis. This review summarizes the most recent advancements in the diagnosis of maternal and prenatal CMV infections.Entities:
Keywords: CMV-ELISPOT; CMV-QuantiFERON; IgG avidity; congenital infections; human cytomegalovirus; imaging; immunoserology; laboratory assays
Mesh:
Year: 2016 PMID: 28031434 PMCID: PMC5328437 DOI: 10.1128/JCM.01868-16
Source DB: PubMed Journal: J Clin Microbiol ISSN: 0095-1137 Impact factor: 5.948