ReviewBrazilian journal of otorhinolaryngology
Hearing loss among patients with Turner's syndrome: literature review.
Review in Brazilian journal of otorhinolaryngology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.
What it found
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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.
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Who cites it
8 citing papers in PubMed, 23 citations in OpenAlex.
- Determinants of Health-Related Quality of Life in Women with Turner Syndrome: The Role of Comorbidities, Hormonal Therapy and Depressive Symptoms.Journal of clinical medicine · 2026Article
- Hearing Loss and Turner Syndrome: A Scoping Review.The journal of international advanced otology · 2025Article
- Turner Syndrome where are we?Orphanet journal of rare diseases · 2024Review
- Disorders of the eye, ear, skin, and nervous system in women with Turner syndrome -a nationwide cohort study.European journal of human genetics : EJHG · 2022Article
- Auditory function and dysfunction: estrogen makes a difference.Cellular and molecular life sciences : CMLS · 2020Review
- Metabolic Syndrome Is not an Independent Risk Factor for Hearing Impairment.The journal of nutrition, health & aging · 2016Article
- Association between cytogenetic alteration and the audiometric profile of individuals with Turner syndrome.Brazilian journal of otorhinolaryngologyArticle
- Endocrine Glands and Hearing: Auditory Manifestations of Various Endocrine and Metabolic Conditions.Indian journal of endocrinology and metabolismReview
Corrections and comments
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Authors and funding
2 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
introductionTurner's syndrome (TS) is caused by a partial or total deletion of an X chromosome, occurring in 1:2,000 to 1:5,000 live born females. Hearing loss is one of its major clinical manifestations. However, there are few studies investigating this problem.
objectivesTo review the current knowledge regarding the epidemiology, etiology, clinical manifestations and diagnosis of hearing impairment in patients with TS.
methodsA bibliographic search was performed in the Medline and Lilacs databanks (1980-2012) to identify the main papers associating Turner's syndrome, hearing impairment and its clinical outcomes.
conclusionsRecurrent otitis media, dysfunction of the Eustachian tube, conductive hearing loss during infancy and sensorineural hearing loss in adolescence are the audiologic disorders more common in ST. The karyotype appears to be important in the hearing loss, with studies demonstrating an increased prevalence in patients with monosomy 45,X or isochromosome 46,i(Xq). Morphologic studies of the cochlea are necessary to help out in the clarifying the etiology of the sensorineural hearing loss.
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Registered trials
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.