Evidence map›Paper›PMID 39936645›Full record

ArticleThe journal of international advanced otology2025

Hearing Loss and Turner Syndrome: A Scoping Review.

Andrea Migliorelli, Andrea Ciorba, Marianna Manuelli, Virginia Corazzi, Francesco Stomeo, Chiara Bianchini, Stefano Pelucchi, Daniele Monzani, Elisabetta Genovese, Silvia Palma

Abstract readScoping Review
In one paragraph

Article in The journal of international advanced otology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Impact of Clinical Factors on Bone Microarchitecture in Patients with Turner Syndrome.Endocrine, metabolic & immune disorders drug targets · 2026
    Article
  2. Review
  3. High frequency of balance abnormalities in Turner syndrome.Brazilian journal of otorhinolaryngology
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Andrea MigliorelliDepartment of Neurosciences, ENT and Audiology Unit, University Hospital of Ferrara, Ferrara, Italy.ORCID 0009-0004-8980-3877
Andrea CiorbaDepartment of Neurosciences, ENT and Audiology Unit, University Hospital of Ferrara, Ferrara, Italy.ORCID 0000-0003-3455-2295
Marianna ManuelliDepartment of Neurosciences, ENT and Audiology Unit, University Hospital of Ferrara, Ferrara, Italy.
Virginia CorazziDepartment of Neurosciences, ENT and Audiology Unit, University Hospital of Ferrara, Ferrara, Italy.
Francesco StomeoDepartment of Neurosciences, ENT and Audiology Unit, University Hospital of Ferrara, Ferrara, Italy.
Chiara BianchiniDepartment of Neurosciences, ENT and Audiology Unit, University Hospital of Ferrara, Ferrara, Italy.ORCID 0000-0002-5115-6107
Stefano PelucchiDepartment of Neurosciences, ENT and Audiology Unit, University Hospital of Ferrara, Ferrara, Italy.
Daniele MonzaniDepartment of ENT and Audiology, University of Verona, Verona, Italy.
Elisabetta GenoveseDepartment of ENT and Audiology, University of Modena and Reggio Emilia, Modena, Italy.
Silvia PalmaDepartment of ENT and Audiology, University of Modena and Reggio Emilia, Modena, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hearing loss (HL) is one of the most frequent disorders in Turner syndrome (TS); HL can be present with a wide spectrum of manifestations and also evolve with age. The aim of this paper is to perform a review of the literature on the prevalence of HL in TS patients also analyzing the possible genetic alterations underlying the auditory features. A review of the literature was performed using PubMed/MEDLINE, EMBASE, and Cochrane Library databases, according to the preferred reporting items for systematic reviews and meta-analyses criteria for scoping reviews (from 2000 to December 2023). A total of 17 articles and 2129 patients with TS have been included; the majority of studies focused on young women/girls, with a mean age range from 2 to 43.6 years. External and middle ear problems, inducing conductive and mixed HL, have been reported to be more frequent in childhood, while sensorineural HL has been described since adolescence. Monosomy 45,X and loss of the X chromosome short arm (p) are the alterations most frequently associated with HL. To date, the pathophysiological mechanisms related to HL in TS are still not fully understood; further studies are necessary to clarify these features and to offer therapies or prevention strategies to avoid the progression of HL in TS subjects.

Indexed as

Hearing LossTurner SyndromeAdolescentAdultChildChild, PreschoolFemaleHearing Loss, SensorineuralHumansPrevalenceYoung Adult

Identifiers

PMID39936645
PMCPMC11843325

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.