Evidence map›Paper›PMID 39677130›Full record

ArticleCureus2024

Vanishing White Matter Disease in Children: An Unusual Association, a Novel Mutation, and a Literature Review.

Zahra Alsahlawi, Hasan M Isa, Sulaiman Alresias, Sayed Mohamed Hasan, Husain A Malalla, Ayman K Ebrahim, Khadija Ali

Abstract readCase Reports
In one paragraph

Article in Cureus, 2024. 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. Article
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

7 authors.

Zahra AlsahlawiDepartment of Pediatrics, Arabian Gulf University, Manama, BHR.
Hasan M IsaDepartment of Pediatrics, Arabian Gulf University, Manama, BHR.
Sulaiman AlresiasDepartment of Pediatrics, Salmaniya Medical Complex, Manama, BHR.
Sayed Mohamed HasanDepartment of Pediatrics, Salmaniya Medical Complex, Manama, BHR.
Husain A MalallaDepartment of Neurology, Salmaniya Medical Complex, Manama, BHR.
Ayman K EbrahimDepartment of Neurology, Salmaniya Medical Complex, Manama, BHR.
Khadija AliDepartment of Pediatrics, Salmaniya Medical Complex, Manama, BHR.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Vanishing white matter (VWM) disease is an autosomal recessive disorder caused by mutations in the gene EIF2B encoding the subunits 1-5 of eukaryotic initiation factor 2B. Although rare, with a reported prevalence of 1:80,000 (0.001%), it was considered as one of the most common leukodystrophies. However, the worldwide incidence and prevalence of this disease are not clear. In Bahrain, of 21 patients who were diagnosed with leukodystrophy, two patients were found to have VWM disease accounting for 9.5%. Vaccinations and infections were the trigger factors for this disease to manifest. Rapid neurological deterioration, loss of developmental milestones, and seizure disorders are the main presentations in both patients. Magnetic resonance imaging (MRI) showed the classical radiological changes of demyelination and leukodystrophy. Patient 1 had associated ulcerative colitis, a finding that was not reported before. Patient 1's condition progressed to a vegetative stage, while patient 2 passed away, reflecting the poor disease outcome. In patient 2, a novel homozygous missense mutation was found in the EIF2B3 gene (c.25G>A, p.Ala9Thr). In this report, we present in detail the prevalence of VWM disease among cases with leukodystrophy, patients' characteristics, clinical presentations, radiological findings, associated diseases, genetic results, and clinical outcomes in the main tertiary hospital in Bahrain between 1998 and 2024. Moreover, we conducted a thorough literature review on this rare condition.

Indexed as

bahrainchildrenleukodystrophyleukoencephalopathies leukoencephalopathy with vanishing white matternovel mutation

Identifiers

PMID39677130
PMCPMC11645671

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