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

Concomitant imaging and genetic findings in children with unilateral sensorineural hearing loss.

The Journal of laryngology and otology - 1 Aug 2017

Gruber M, Brown C, Mahadevan M, Neeff M

Abstract excerpt

OBJECTIVE: To describe the concomitant imaging and genetic findings in children diagnosed with non-syndromic unilateral sensorineural hearing loss. METHODS: A retrospective cohort study was conducted of 60 children diagnosed between January 2005 and December 2015 in a tertiary-level paediatric institution. RESULTS: Average age at diagnosis was 4.3 years. All children were considered non-syndromic. Hearing loss...

Read the complete abstract on PubMed

Topics

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

Share to Child
Share to Child, Preschool
Share to Connexin 26

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Connexins

Share to GJB2 gene

Share to Magnetic Resonance Imaging

Share to Mutation

Share to Tomography, X-Ray Computed

Source

Identifiers

PMID: 28651654
DOI: 10.1017/S0022215117001219

Genes

GJB2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Concomitant imaging and genetic findings in children with unilateral sensorineural hearing loss.PMID 28651654Read ↗

The Yield of Multigene Testing in the Management of Pediatric Unilateral Sensorineural Hearing Loss.Semantic proximity Read ↗

Genetic Underpinnings and Audiological Characteristics in Children with Unilateral Sensorineural Hearing LossSemantic proximity Read ↗

Outcomes of evaluation and testing of 660 individuals with hearing loss in a pediatric genetics of hearing loss clinic.Semantic proximity Read ↗

Audiologic and temporal bone imaging findings in patients with sensorineural hearing loss and GJB2 mutations.Semantic proximity Read ↗

Evaluation and management of nonsyndromic congenital hearing loss.Semantic proximity Read ↗

Etiologic and Audiologic Characteristics of Patients With Pediatric-Onset Unilateral and Asymmetric Sensorineural Hearing Loss.Semantic proximity Read ↗

Genetic and Non-genetic Workup for Pediatric Congenital Hearing LossSemantic proximity Read ↗

Additional clinical manifestations in children with sensorineural hearing loss and biallelic GJB2 mutations: who should be offered GJB2 testing?Semantic proximity Read ↗

Comprehensive genetic testing improves the clinical diagnosis and medical management of pediatric patients with isolated hearing loss.Semantic proximity Read ↗

Syndromic Hearing Loss: A Brief Review of Common Presentations and GeneticsSemantic proximity Read ↗

Diagnostic yield in the workup of congenital sensorineural hearing loss is dependent on patient ethnicity.Semantic proximity Read ↗

Children with GJB2 gene mutations have various audiological phenotypes.Semantic proximity Read ↗

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