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

Audio profiles in mitochondrial deafness m.1555A>G and m.3243A>G show distinct differences.

Medical science monitor : international medical journal of experimental and clinical research - 6 Mar 2015

Iwanicka-Pronicka Katarzyna, Pollak Agnieszka, Skórka Agata, Lechowicz Urszula, Korniszewski Lech, Westfal Przemysław, Skarżyński Henryk, Płoski Rafał

Abstract excerpt

BACKGROUND: Hearing loss is one of the most common symptoms of mitochondrial disorders. However, audiological phenotypes associated with different molecular defects in mtDNA are not yet well characterized. MATERIAL AND METHODS: A large cohort of 1499 nonconsanguineous patients aged 5-40 years with hearing loss of unknown etiology was screened for mutations in mtDNA. For further analysis, patients harboring...

Read the complete abstract on PubMed

Topics

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

Share to Audiometry
Share to Auditory Threshold

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Child, Preschool

Share to Deafness

Share to DNA, Mitochondrial

Share to Hearing Loss

Share to Mitochondria

Share to Young Adult

Source

Open in PubMed Open full text

Identifiers

PMID: 25744662
DOI: 10.12659/MSM.890965
PMCID: PMC4360812

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

Audio profiles in mitochondrial deafness m.1555A>G and m.3243A>G show distinct differences.PMID 25744662Read ↗

The clinical and audiologic features of hearing loss due to mitochondrial mutations.Semantic proximity Read ↗

Audiological and genetic features of the mtDNA mutations.Semantic proximity Read ↗

Sensorineural hearing loss caused by mitochondrial DNA mutations: special reference to the A1555G mutation.Semantic proximity Read ↗

Analysis of mitochondrial alterations in Brazilian patients with sensorineural hearing loss using MALDI-TOF mass spectrometry.Semantic proximity Read ↗

Clinical characteristics and hearing impairment in carriers of the m.3243 A > G variant.Semantic proximity Read ↗

Prevalence and Clinical Characteristics of Mitochondrial DNA Mutations in Korean Patients With Sensorineural Hearing Loss.Semantic proximity Read ↗

Audiological features and mitochondrial DNA sequence in a large family carrying mitochondrial A1555G mutation without use of aminoglycoside.Semantic proximity Read ↗

Defining the cellular and molecular mechanism of maternally inherited hearing lossSemantic proximity Read ↗

Audiological follow-up of children with the m.1555A>G mutation in mitochondrial DNA.Semantic proximity Read ↗

Audiovestibular findings in patients with mitochondrial A1555G mutation.Semantic proximity Read ↗

Heteroplasmy levels of mtDNA1555A>G mutation is positively associated with diverse phenotypes and mutation transmission in a Chinese family.Semantic proximity Read ↗

The A1555G mtDNA mutation in Danish hearing-impaired patients: frequency and clinical signs.Semantic proximity Read ↗

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