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

Is hearing loss due to mutations in the Connexin 26 gene progressive?

International journal of audiology - 1 Jan 2008

Gopalarao Deepika, Kimberling William J, Jesteadt Walt, Kelley Philip M, Beauchaine Kathryn L, Cohn Edward S

Abstract excerpt

Serial audiograms were analysed for seven subjects, who were homozygous for the 35delG GJB2 mutation. The criterion for determining progression of hearing loss was at least a 1-dB loss in air conduction pure-tone average-3 (ACPTA-3) or ACPTA-4 per year for 2 to 10 years, with a minimum change of...

Read the complete abstract on PubMed

Topics

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

Share to Audiometry, Pure-Tone
Share to Auditory Threshold
Share to Connexin 26

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Connexins

Share to Disease Progression

Share to Follow-Up Studies

Share to Hearing Loss, Sensorineural

Share to Homozygote

Source

Identifiers

PMID: 18196482
DOI: 10.1080/14992020701602087

Genes

GJB2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-18196482-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Is hearing loss due to mutations in the Connexin 26 gene progressive?PMID 18196482Read ↗

Connexin-26-associated deafness: phenotypic variability and progression of hearing loss.Semantic proximity Read ↗

Cx26 gene mutations in idiopathic progressive hearing loss.Semantic proximity Read ↗

Longitudinal phenotypic analysis in patients with connexin 26 (GJB2) (DFNB1) and connexin 30 (GJB6) mutations.Semantic proximity Read ↗

Sudden hearing loss in a family with GJB2 related progressive deafness.Semantic proximity Read ↗

Audiologic phenotype and progression in GJB2 (Connexin 26) hearing loss.Semantic proximity Read ↗

Novel connexin 30 and connexin 26 mutational spectrum in patients with progressive sensorineural hearing loss.Semantic proximity Read ↗

Clinical studies of families with hearing loss attributable to mutations in the connexin 26 gene (GJB2/DFNB1)Semantic proximity Read ↗

Hearing impairment in Dutch patients with connexin 26 (GJB2) and connexin 30 (GJB6) mutations.Semantic proximity Read ↗

[Progressive hearing impairment with deletion in GJB2 gene despite normal newborn hearing screening].Semantic proximity Read ↗

Hearing and Hearing Loss Progression in Patients with GJB2 Gene Mutations: A Long-Term Follow-Up.Semantic proximity Read ↗

Clinical features of the prevalent form of childhood deafness, DFNB1, due to a connexin-26 gene defect: implications for genetic counselling.Semantic proximity Read ↗

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

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