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

Early deterioration of residual hearing in patients with SLC26A4 mutations.

The Laryngoscope - 1 Aug 2016

Kim Bo Gyung, Roh Kyung Jin, Park Ah Young, Lee Seung Chul, Kang Bo Sung, Seo Young Joon, Lee Jong Dae, Choi Jae Young

Abstract excerpt

OBJECTIVES/HYPOTHESIS: To compare changes in hearing in patients with SLC26A4 during early and late childhood. STUDY DESIGN: Retrospective chart review. METHODS: A total of 102 patients with biallelic SLC26A4 mutations visited the tertiary referral otolaryngology department between March 2005 and February 2015. Newborn hearing screening tests had been performed on 22 of these patients. We analyzed 26 patients who...

Read the complete abstract on PubMed

Topics

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

Share to Age Factors
Share to Child, Preschool
Share to Hearing Loss

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Hearing Tests

Share to Infant

Share to Infant, Newborn

Share to Membrane Transport Proteins

Share to Sulfate Transporters

Source

Identifiers

PMID: 26650914
DOI: 10.1002/lary.25786

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

Early deterioration of residual hearing in patients with SLC26A4 mutations.PMID 26650914Read ↗

Natural Course of Residual Hearing with Reference to GJB2 and SLC26A4 Genotypes: Clinical Implications for Hearing Rehabilitation.Semantic proximity Read ↗

Newborn Hearing Screening to Diagnosis: A Clinical Study of 15,818 CasesSemantic proximity Read ↗

Hearing Progression of Children with Enlarged Vestibular Aqueduct (EVA) According to<i>SLC26A4</i>Genetic Mutation StatusSemantic proximity Read ↗

Newborn genetic screening for hearing impairment: a population-based longitudinal study.Semantic proximity Read ↗

[Research progress on the etiology of delayed-onset hearing loss in children].Semantic proximity Read ↗

Prenatal diagnosis of SLC26A4 mutation and delayed onset of hearing loss.Semantic proximity Read ↗

Hearing loss associated with enlarged vestibular aqueduct and zero or one mutant allele of SLC26A4.Semantic proximity Read ↗

Connexin 26 deafness is not always congenital.Semantic proximity Read ↗

Limitations of hearing screening in newborns with PDS mutations.Semantic proximity Read ↗

Hearing Preservation During Cochlear Implantation and Electroacoustic Stimulation in Patients With SLC26A4 Mutations.Semantic proximity Read ↗

Moderate-Severe Hearing Loss in Children: A Diagnostic and Rehabilitative Challenge.Semantic proximity Read ↗

Vestibular function is associated with residual low-frequency hearing loss in patients with bi-allelic mutations in the SLC26A4 gene.Semantic proximity Read ↗

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