Evidence map›Paper›PMID 41784708›Full record

Observational studyActa neurologica Belgica2026

Genetic and therapeutic insights in musician's dystonia: a single-centre case series and narrative review.

David Aktan, Charlotte Mouraux, Frédérique Depierreux

Abstract readObservational Study
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In one paragraph

Observational study in Acta neurologica Belgica, 2026. 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

3 authors.

David AktanRare Movement Disorders (RMD) Research Group, GIGA - CRC in vivo imaging unit, University of Liege, Liege, Belgium.ORCID http://orcid.org/0009-0006-6948-9133
Charlotte MourauxRare Movement Disorders (RMD) Research Group, GIGA - CRC in vivo imaging unit, University of Liege, Liege, Belgium.ORCID http://orcid.org/0000-0001-9569-9229
Frédérique DepierreuxRare Movement Disorders (RMD) Research Group, GIGA - CRC in vivo imaging unit, University of Liege, Liege, Belgium. Frederique.Depierreux@chuliege.be.ORCID http://orcid.org/0000-0001-7949-8611

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMusician’s dystonia is a task-specific focal dystonia that severely impacts professional performance and quality of life. Literature combining clinical data and therapeutic outcomes remains limited.

objectivesTo describe the clinical characteristics, genetic findings, and treatment outcomes in a cohort of musicians with dystonia, and to contextualise these data within current evidence.

methodsThis prospective, monocentric observational study included 20 patients diagnosed with musician’s dystonia at a tertiary movement disorder centre (October 2023 – October 2025). Data collected included demographics, instrument type, dystonia phenomenology, targeted genetic testing, and treatments received. Outcomes were assessed both clinically and subjectively.

resultsThe cohort comprised 16 males and 4 females (mean age at onset: 38 years). Instruments included keyboards (40%), strings (35%), and wind instruments (25%). Two patients carried TOR1A variants. Botulinum toxin injections were performed in 15 cases, with partial improvement in 80%. Sensorimotor retraining was used in 10 patients. Career impact was substantial, with 30% reporting career termination.

conclusionsMusician’s dystonia is heterogeneous and often career-threatening. Our findings highlight the importance of early diagnosis, genetic screening in selected cases, and multimodal management combining botulinum toxin and rehabilitative approaches.

Indexed as

Dystonic DisordersMusicAdultBotulinum ToxinsFemaleHumansMaleMiddle AgedMolecular ChaperonesProspective StudiesYoung AdultBotulinum ToxinsMolecular ChaperonesTOR1A protein, humanFocal dystoniaMusician’s dystoniaNeurogeneticsRare movement disordersTask-specific dystonia

Identifiers

PMID41784708

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.