Evidence map›Paper›PMID 41964125›Full record

ArticleAnnals of Indian Academy of Neurology2026

Hirayama Disease: Latest Insights into an Intriguing Disorder.

Dipti Baskar, Atchayaram Nalini, Seena Vengalil

Abstract read
In one paragraph

Article in Annals of Indian Academy of Neurology, 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.

Dipti BaskarDepartment of Neurology, National Institute of Mental Health and Neuro Sciences, Bengaluru, Karnataka, India.
Atchayaram Nalini
Seena Vengalil

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

abstractHirayama disease (HD) is a cervical flexion-induced myelopathy that causes asymmetrical distal upper limb atrophy and weakening. It usually affects males, with onset in early adolescence, and progression occurs over 3-5 years, resulting in irreversible functional deficits. In addition to classical HD, several rarer phenotypes are described, including distal bimelic amyotrophy, lower limb, proximal, and upper motor neuron variants. Dynamic flexion magnetic resonance imaging is critical in the diagnosis, with distinctive characteristics such as significant epidural flow voids and anterior displacement of the posterior dural sac involving lower cervical segments, with sensitivity and specificity of 93% and 98%, respectively. In progressive cases, apart from conservative management with a cervical collar, surgical management is considered early, with the ideal approach being anterior cervical discectomy and fusion with plating. This review aims to address the latest insights in the pathophysiology, HD variants, spine imaging, and various surgical procedures in the management and prevention of serious residual limb weakness.

Indexed as

brachial monomelic amyotrophycervical flexion induced myelopathydistal bimelic amyotrophydynamic magnetic resonance imagingHirayama diseasemonomelic amyotrophy

Identifiers

PMID41964125
PMCPMC13193633

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.