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the claim

Various medical conditions cause a reduced hearing range

the verdict
SUPPORTED
the evidence backs this
Recorded sources
4 sources for · 0 against

Counts group repeated records of the same source within each side. They do not measure evidence strength or source independence.

Various medical conditions and etiologies, including genetic variants and neurological disorders, are well-documented to cause reduced hearing ranges such as high-frequency or low-frequency hearing loss.

The analysis

The claim states that various medical conditions cause a reduced hearing range. Multiple papers discuss specific medical conditions, etiologies, and genetic variants associated with different types of hearing loss (e.g., high-frequency hearing loss in essential tremor, genetic variants causing hearing loss, and etiology-based sensorineural hearing loss). Therefore, the claim is supported by the literature.

Evidence for · 4
Recorded source metadata

Kim CH, Choi BY. Etiology-Driven Personalized Cochlear Implantation: Implications for Electrode Choice, Timing, and Outcomes.. 2026. https://doi.org/10.3390/jpm16030130

Paper [2] discusses etiology-driven cochlear implantation for various sensorineural hearing loss conditions affecting hearing ranges.

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More for · 3
Recorded source metadata

Lee J, Yoon CY, Kim J, Seo YJ. Prognostic Significance of Isolated Low-Frequency Hearing Loss: A Longitudinal Audiometric Study.. 2025. https://doi.org/10.3390/jcm14196749

Paper [3] classifies hearing loss types like high-frequency and low-frequency hearing loss linked to various underlying conditions and age.

Recorded source metadata

Yıldız HY, İşeri M, İşeri P. An Exploratory Study of Auditory Brainstem Responses and Hearing Thresholds in Essential Tremor.. 2026. https://doi.org/10.3390/medicina62030495

Paper [5] reports that essential tremor is associated with a higher prevalence of high-frequency hearing loss.

Recorded source metadata

Peng LT, Wang WQ, Huang SS, Liu M, Yang SY, Kang DY, Wang X, Gao X, Yuan YY, Xu JC. A Novel Frameshift Variant c.1023_1029del (p.Asp342ArgfsTer54) Leading to Extended Incorrect Protein C Termini in HOMER2 Causing Autosomal Dominant Nonsyndromic Hearing Loss.. 2026. https://doi.org/10.1002/jcla.70137

Paper [6] identifies a novel genetic variant in HOMER2 causing autosomal dominant nonsyndromic hearing loss affecting frequency ranges.

The paper trail · every fact has a biography
first checked02 Aug 2026
judged → SUPPORTED · 7502 Aug 2026
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