Evidence map›Paper›PMID 37399346›Full record

ArticleBMJ case reports2023

Lateral semicircular canal dilatation in a patient with congenital hearing loss due to α-tectorin mutation: microanatomical considerations.

Anastasios Goulioumis, Michalis Athanasopoulos, Kleanthi Kalogerakou, Kostis Gyftopoulos

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

Article in BMJ case reports, 2023. 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
0.1field-weighted citation impact, top 53% 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

4 authors at 3 institutions in 1 country.

Anastasios GoulioumisOtorhinolaryngology, Karamandanio Children's Hospital, Patras, Greece goulioum@upatras.gr.ORCID http://orcid.org/0000-0003-3178-2618
Michalis AthanasopoulosOtorhinolaryngology, Karamandanio Children's Hospital, Patras, Greece.ORCID http://orcid.org/0000-0003-0592-6921
Kleanthi KalogerakouCT and MRI, Athens Medical Centre, Athens, Greece.
Kostis GyftopoulosAnatomy, University of Patras School of Health Sciences, Patras, Greece.
University of Patras · GRAthens Medical Center · GRGeneral Hospital Pediatric Karamandanio · GR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The tectorial membrane is crucial in the physiology of the auditory neuroepithelium. Mutations in one of its functional molecules, α-tectorin, lead to autosomal dominant and recessive congenital mid-frequency, non-syndromic hearing loss.Typically, α-tectorin mutations are not accompanied by any morphological abnormalities of the labyrinth. For the first time, we present a case of a toddler boy with congenital hearing loss due to

Indexed as

DeafnessHearing Loss, SensorineuralDilatationGPI-Linked ProteinsHumansMaleMutationSemicircular CanalsGPI-Linked ProteinsCongenital disordersEar, nose and throat/otolaryngologyGenetics

Identifiers

PMID37399346
PMCPMC10314528
OpenAlexW4382657607

What OpenQuestion holds

Textmetadata
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.