Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Genotypic diversity and mixed infection in newborn disease and hearing loss in congenital cytomegalovirus infection.

The Pediatric infectious disease journal - 1 Oct 2013

Pati Sunil K, Pinninti Swetha, Novak Zdenek, Chowdhury Nazma, Patro Raj K, Fowler Karen, Ross Shannon, Boppana Suresh

Abstract excerpt

BACKGROUND: Congenital cytomegalovirus (cCMV) is a common congenital infection and a leading nongenetic cause of sensorineural hearing loss (SNHL). CMV exhibits extensive genetic variability, and infection with multiple CMV strains (mixed infection) was shown to be common in congenital CMV. The role of mixed infections in disease and outcome remains to be defined. METHODS: Genotyping of envelope glycoproteins,...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Cohort Studies
Share to Coinfection

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Cytomegalovirus

Share to Cytomegalovirus Infections

Share to Hearing Loss, Sensorineural

Share to Infant, Newborn

Share to Saliva

Share to Viral Load

Source

Open in PubMed Open full text

Identifiers

PMID: 23694837
DOI: 10.1097/INF.0b013e31829bb0b9
PMCID: PMC3785554

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Genotypic diversity and mixed infection in newborn disease and hearing loss in congenital cytomegalovirus infection.PMID 23694837Read ↗

Association of CMV genomic mutations with symptomatic infection and hearing loss in congenital CMV infection.Semantic proximity Read ↗

Mixed infection and strain diversity in congenital cytomegalovirus infection.Semantic proximity Read ↗

Viral shedding, and distribution of cytomegalovirus glycoprotein H (UL75), glycoprotein B (UL55), and glycoprotein N (UL73) genotypes in congenital cytomegalovirus infection.Semantic proximity Read ↗

Distribution of CMV envelope glycoprotein B, H and N genotypes in infants with congenital cytomegalovirus symptomatic infectionSemantic proximity Read ↗

Characterization of a universal screening approach for congenital CMV infection based on a highly-sensitive, quantitative, multiplex real-time PCR assaySemantic proximity Read ↗

Cytomegalovirus glycoprotein H genotype distribution and the relationship with hearing loss in children.Semantic proximity Read ↗

Hearing Loss in Infants and Children with Asymptomatic Congenital Cytomegalovirus Infection: An Update in Diagnosis, Screening and TreatmentSemantic proximity Read ↗

Cytomegalovirus Genetic Diversity Following Primary Infection.Semantic proximity Read ↗

Human cytomegalovirus UL55, UL144, and US28 genotype distribution in infants infected congenitally or postnatally.Semantic proximity Read ↗

Detection of cytomegalovirus DNA in dried blood spots of Minnesota infants who do not pass newborn hearing screening.Semantic proximity Read ↗

Analysis of human cytomegalovirus strain populations in urine samples of newborns by ultra deep sequencing.Semantic proximity Read ↗

Prevalence of cytomegalovirus DNAemia and genotypic distribution among childbearing mothers and neonates in Taiwan.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.