Evidence map›Paper›PMID 36873670›Full record

ArticleIntractable & rare diseases research2023

Re-evaluation of the symptoms of Hirayama disease through anatomical perspective.

Bahar Tekin, Gamze Ansen, Tugrul Ormeci, Nesrin Helvaci Yilmaz, Bayram Ufuk Sakul

Open access · diamondAbstract read
In one paragraph

Article in Intractable & rare diseases research, 2023. 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, top 97% of its field
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, 0 citations in OpenAlex.

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

5 authors at 1 institution in 1 country.

Bahar TekinDepartment of Anatomy, Faculty of Medicine, Istanbul Medipol University, Istanbul, Turkey.
Gamze AnsenDepartment of Anatomy, Faculty of Medicine, Istanbul Medipol University, Istanbul, Turkey.
Tugrul OrmeciDepartment of Radiology, Faculty of Medicine, Istanbul Medipol University, Istanbul, Turkey.
Nesrin Helvaci YilmazDepartment of Neurology, Faculty of Medicine, Istanbul Medipol University, Istanbul, Turkey.
Bayram Ufuk SakulDepartment of Anatomy, Faculty of Medicine, Istanbul Medipol University, Istanbul, Turkey.
Istanbul Medipol University · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hirayama disease is a rare disease of the anterior horn motor neuron caused by compression of the cervical spinal cord when the neck is flexed. Cervical myelopathy may accompany the disease. It is characterized by symmetrical or asymmetrical muscle weakness and atrophy of muscles innervated by lower cervical and upper thoracic motor neurons. We recorded two male cases of Hirayama disease between the ages of 15 and 21 based on magnetic resonance imaging (MRI) features obtained from the cervical neutral state and from the flexion position which appeared in the right upper extremity. Loss of strength and atrophy in the right upper extremities was existent in clinical findings of these patients. When MRI was taken in the flexion position, there were dilated veins as hypointense signal void on T2 weighted series in posterior epidural area. The contrast enhancement was seen on these veins. It was observed that the posterior dura was displaced anteriorly and the anterior subarachnoid space was narrow. In cases which show clinical findings such as atrophy and loss of strength, having normal MRI results obtained in the neutral position makes it difficult to diagnose Hirayama Disease. In case of a suspicion of Hirayama disease the diagnosis can be made more easily by MRI taken in the flexion position. These case reports aim to bring Hirayama disease to mind and optimize the management of affected individuals.

Indexed as

cervical MRIcervical myelopathyHirayamaJuvenile spinal muscular atrophyMonomelic amyotrophy

Identifiers

PMID36873670
PMCPMC9976093
OpenAlexW4321608922

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.