Evidence map›Paper›PMID 34167184›Full record

ArticleJournal of audiology & otology2021

Familial Otosclerosis Associated with Osteogenesis Imperfecta: A Case Report.

Ha Neul Lee, Hyun Jong Jeon, Young Joon Seo

Open access · diamondAbstract readCase Reports
PubMed Full text at PMC Publisher
In one paragraph

Article in Journal of audiology & otology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 93% of its field
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

0 citing papers in PubMed, 1 citations in OpenAlex.

No citing paper in PubMed yet.

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

3 authors at 1 institution in 1 country.

Ha Neul LeeDepartment of Otorhinolaryngology-Head and Neck Surgery, Research Institute of Hearing Enhancement, Yonsei University Wonju College of Medicine, Wonju, Korea.
Hyun Jong JeonDepartment of Otorhinolaryngology-Head and Neck Surgery, Research Institute of Hearing Enhancement, Yonsei University Wonju College of Medicine, Wonju, Korea.
Young Joon SeoDepartment of Otorhinolaryngology-Head and Neck Surgery, Research Institute of Hearing Enhancement, Yonsei University Wonju College of Medicine, Wonju, Korea.
Yonsei University · KR

Funding

Ministry of Science and ICTNational Information Society AgencyNational Research Foundation of Korea 2020R1A2C1009789
6 · The paper itself

Abstract

Otosclerosis, a hereditary disorder characterized by disordered resorption and deposition of bone, results in progressive hearing loss. Osteogenesis imperfecta (OI) is a genetic disorder characterized by recurrent fractures, blue sclera, and varying degrees of hearing impairment; and is a known risk factor for otosclerosis. After adolescence, the risk of fracture decreases, reducing the need for follow-up in OI. However, otosclerosis is a progressive disorder. In this report, we discuss two cases of familial otosclerosis with different clinical features. We hypothesize that the difference in hearing level correlates with the difference in computed tomography findings. The mother, whose case was considered severe, was prescribed hearing aids, while the daughter, who had normal hearing level, was regularly followed up.

Indexed as

Familial otosclerosisHearing lossHereditary disorderOsteogenesis imperfectaOtosclerosis

Identifiers

PMID34167184
PMCPMC8524114
OpenAlexW3173411339

What OpenQuestion holds

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LicenceCC BY-NC
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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.