Evidence map›Paper›PMID 42527583›Full record

ArticleEuropean journal of human genetics : EJHG2026

PALM3 and hearing loss: a potential dual diagnosis interfering with novel gene discovery.

Paria Najarzadeh Torbati, Lukas Hallbrucker, Michaela A H Hofrichter, Daniel Owrang, Jonas Setzke, Manfred W Kilimann, Anahid Hemmatpour, Mohsen Rajati, Ehsan Ghayoor Karimiani, Thomas Haaf and 2 more

Abstract readCase Reports
In one paragraph

Article in European journal of human genetics : EJHG, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Genomics cycle: discover, diagnose, interpret, act.European journal of human genetics : EJHG · 2026
    Article
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

12 authors.

Paria Najarzadeh TorbatiDepartment of Medical Genetics, Next Generation Genetic Polyclinic, Mashhad, Iran.
Lukas HallbruckerAuditory Neuroscience Group, Institute of Physiology, Medical University Innsbruck, Innsbruck, Austria.
Michaela A H HofrichterInstitute of Clinical Genetics and Genomic Medicine, University Hospital Würzburg, Würzburg, Germany.
Daniel OwrangInstitute for Auditory Neuroscience and Inner Ear Lab, University Medical Center Göttingen, Göttingen, Germany.
Jonas SetzkeInstitute for Auditory Neuroscience and Inner Ear Lab, University Medical Center Göttingen, Göttingen, Germany.
Manfred W KilimannMax-Planck-Institute for Multidisciplinary Sciences (City Campus), Göttingen, Germany.
Anahid HemmatpourDepartment of Medical Genetics, Next Generation Genetic Polyclinic, Mashhad, Iran.
Mohsen RajatiDepartment of Otorhinolaryngology, School of Medicine, Ghaem Hospital, Sinus and Surgical Endoscopic Research Center, Mashhad University of Medical Sciences, Mashhad, Iran.
Ehsan Ghayoor KarimianiDepartment of Medical Genetics, Next Generation Genetic Polyclinic, Mashhad, Iran.
Thomas HaafInstitute of Human Genetics, Julius-Maximilians-University Würzburg, Würzburg, Germany.ORCID http://orcid.org/0000-0002-0737-0763
Christian VoglAuditory Neuroscience Group, Institute of Physiology, Medical University Innsbruck, Innsbruck, Austria.ORCID http://orcid.org/0000-0003-4432-2733
Barbara VonaInstitute for Auditory Neuroscience and Inner Ear Lab, University Medical Center Göttingen, Göttingen, Germany. barbara.vona@med.uni-goettingen.de.ORCID http://orcid.org/0000-0002-6719-3447

Funding

Austrian Science Fund (Fonds zur Förderung der Wissenschaftlichen Forschung) 10.55776/PIN5995324Deutsche Forschungsgemeinschaft (German Research Foundation) Collaborative Research Center 1690 (Project A03)Deutsche Forschungsgemeinschaft (German Research Foundation) VO 2138/7-1 grant 469177153Deutsche Forschungsgemeinschaft (German Research Foundation) VO 2138/8-1 grant 543719215
6 · The paper itself

Abstract

Hereditary hearing loss is highly genetically heterogeneous, with emerging overlap between genes implicated in early-onset and age-related hearing loss. We report a consanguineous family with autosomal recessive, non-syndromic hearing loss in which the proband harbors a homozygous splice-site variant in PALM3 NM_001145028.2:c.314+1G>A and a homozygous missense variant in OTOA NM_144672.4:c.1939G>C p.(Gly647Arg). A minigene assay for the PALM3 variant demonstrated aberrant splicing with exon skipping, resulting in either a frameshift or a large in-frame deletion, both consistent with loss of function and impacting all known transcripts. While the organ of Corti from 12-month-old heterozygous Palm3 mice showed preserved overall architecture, a study describing Palm3 knockout mice exhibit auditory dysfunction, supporting a possible auditory phenotype with loss of function. Although a dual molecular diagnosis cannot be excluded, the combined genetic, functional, and comparative data support PALM3 as a candidate gene potentially contributing to autosomal recessive hearing loss.

Indexed as

Hearing LossAnimalsFemaleGasderminsHomozygoteHumansMaleMiceMice, KnockoutMutation, MissenseNerve Tissue ProteinsPedigreeGasderminsNerve Tissue ProteinsPJVK protein, human

Identifiers

PMID42527583
PMCPMC13634051

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.