Evidence map›Paper›PMID 40727136›Full record

ArticleIndian journal of otolaryngology and head and neck surgery : official publication of the Association of Otolaryngologists of India2025

Characteristics of Hearing Loss in Patients with

María Fábrega-Torrano, Rocío González-Aguado, Esther Onecha, Carmelo Morales-Angulo

Abstract read
In one paragraph

Article in Indian journal of otolaryngology and head and neck surgery : official publication of the Association of Otolaryngologists of India, 2025. 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
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.

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

4 authors.

María Fábrega-TorranoFacultad de Medicina, Universidad de Cantabria, Santander, Spain.
Rocío González-AguadoFacultad de Medicina, Universidad de Cantabria, Santander, Spain.ORCID 0000-0002-4407-287X
Esther OnechaDepartment of Genetics, Hospital Universitario Marqués de Valdecilla, Santander, Cantabria Spain.ORCID 0000-0002-8631-3555
Carmelo Morales-AnguloFacultad de Medicina, Universidad de Cantabria, Santander, Spain.ORCID 0000-0002-4268-2762

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Stickler syndrome type 1 (STL1) is an autosomal dominant genetic disorder that affects connective tissue with highly heterogeneous clinical manifestations, primarily at the ocular, orofacial, skeletal, and auditory levels. The aim of our study was to determine the variability of the auditory phenotype associated with pathogenic variants of the Supplementary Information: The online version contains supplementary material available at 10.1007/s12070-025-05638-7.

Indexed as

Autosomal dominantCOL2A1Genetic hearing lossSensorineural hearing lossStickler Syndrome

Identifiers

PMID40727136
PMCPMC12297190

What OpenQuestion holds

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Registered trials

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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.