Evidence map›Paper›PMID 41969642›Full record

ReviewTremor and other hyperkinetic movements (New York, N.Y.)2026

Childhood-Onset Myoclonus-Dystonia Due to

Yun Lin, Yu Aoh, Ming-Kuei Lu

Abstract readCase ReportsReview
In one paragraph

Review in Tremor and other hyperkinetic movements (New York, N.Y.), 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. Review
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.

Yun LinDivision of Parkinson's Disease and Movement Disorders, Department of Neurology, China Medical University Hospital, Taichung, Taiwan.ORCID 0009-0006-4601-6122
Yu AohDivision of Parkinson's Disease and Movement Disorders, Department of Neurology, China Medical University Hospital, Taichung, Taiwan.ORCID 0000-0001-6985-4168
Ming-Kuei LuDivision of Parkinson's Disease and Movement Disorders, Department of Neurology, China Medical University Hospital, Taichung, Taiwan.ORCID 0000-0002-2768-4399

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Myoclonus-dystonia (M-D) is a rare hyperkinetic movement disorder most commonly associated with Case Report: A 23-year-old man with childhood-onset Tourette-like symptoms developed progressive dystonia, upper-limb-predominant dystonia, upper-limb-predominant myoclonus, and laryngeal involvement. Genetic testing identified a pathogenic Discussion: This case illustrates that Tourette-like manifestations may occur as an early presentation of Highlights: This case describes a genetically confirmed

Indexed as

Dystonic DisordersPotassium ChannelsHumansMaleMutationYoung AdultPotassium ChannelschilddystoniaKCTD17 proteinmovement disordersmyoclonusMyoclonus-dystonia

Identifiers

PMID41969642
PMCPMC13068090

What OpenQuestion holds

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LicenceCC BY
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.