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Record W4416331944 · doi:10.1177/22143602251393910

Unveiling MYH2-related myopathy: Histological-genetic insights from a case series and systematic review

2025· article· en· W4416331944 on OpenAlexaff
Beatrice Labella, Guy Brochier, Maud Beuvin, Emmanuelle Lacène, A. Chanut, A. Madelaine, C. Labasse, Aurélie Méneret, Andreas Roos, Heike Kölbel, Adrian Levine, Grace Yoon, Juliette Svahn, Françoise Bouhour, Nathalie Streichenberger, Aleksandra Nadaj‐Pakleza, Edoardo Malfatti, Guillaume Bassez, Anthony Béhin, Pascal Laforêt, Rocío N. Villar‐Quiles, Sarah Léonard-Louis, Thierry Maisonobe, Tanya Stojkovic, B. Eymard, Norma B. Romero, Alessandro Padovani, Massimiliano Filosto, Denise Cassandrini, Valérie Biancalana, John Rendu, Kiran Polavarapu, Corinne Métay, Teresinha Evangelista

Bibliographic record

VenueJournal of Neuromuscular Diseases · 2025
Typearticle
Languageen
FieldBiochemistry, Genetics and Molecular Biology
TopicConnective tissue disorders research
Canadian institutionsChildren's Hospital of Eastern OntarioSickKids FoundationUniversity of TorontoUniversity of OttawaHospital for Sick Children
FundersEuropean Regional Development FundDeutsche Gesellschaft für Muskelkranke
KeywordsPathologicalPresentation (obstetrics)StainPhenotypeDiseaseGenetic testingCongenital myopathy

Abstract

fetched live from OpenAlex

We report 13 unrelated patients and a systematic review of published cases through 30 October 2024, supplemented by HGMD Pro (2024.2) and LOVD (https://www.lovd.nl/) databases. In the case series, most patients (n = 11/13, 84.6%) exhibited clinical symptoms from early childhood to middle adulthood. The mean age of onset was 22.8 years (vs 7.73 years in literature review), likely because of absence of birth contractures, described in early reports. External ophthalmoparesis, though not a defining feature, should raise suspicion of MYH2-related myopathy in patients with a CPEO-like presentation and limb-girdle weakness. Notably, two patients presented with postural tremor of the upper limbs as their first symptom. Although rimmed vacuoles were a characteristic feature in initial reports of MYH2-related myopathy, they were absent in our case series. The most informative stain was ATPase, detecting the lack or reduction of type 2A fibres. Electron microscopy revealed additional features, such as the presence of cores associated with rods in one patient and pathological subsarcolemmal mitochondrial accumulations in 2 patients. Fifteen novel variants were identified amongst the 13 patients of this study, expanding the current genetic landscape for MYH2-related muscle diseases. The phenotypic and histological diversity observed can not be fully accounted for by genetic factors alone, suggesting the presence of additional contributing factors. This wide variability may lead to under-recognition of this disease, thus the importance of clinicians' awareness on the topic.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame distilled prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. Learned from the 10,348 direct Codex labels and 10,348 direct Gemma labels. Candidate is the union of thresholded teacher heads; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels or direct frontier model labels.

metaresearch head score (Codex)0.000
metaresearch head score (Gemma)0.002
Version: codex-gemma-dda1882f352aValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Systematic review · Consensus signal: none
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.484
Threshold uncertainty score0.557

Codex and Gemma teacher scores by category

CategoryCodexGemma
Metaresearch0.0000.002
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0010.000
Bibliometrics0.0000.000
Science and technology studies0.0000.000
Scholarly communication0.0000.000
Open science0.0000.000
Research integrity0.0000.000
Insufficient payload (model declined to judge)0.0000.000

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.008
GPT teacher head0.265
Teacher spread0.258 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one teacher head, not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designSystematic review
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

Quick stats

Citations1
Published2025
Admission routes1
Has abstractyes

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