Evidence map›Paper›PMID 40486355›Full record

ArticleCureus2025

A Very Rare Variant of Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leucoencephalopathy (CADASIL) on the gnomAD Database With Variable Phenotypic Expression.

Ikechukwu Chukwuocha, Solomon Eigbe, Di Liang, Baig Al-Moyeed

Abstract readCase Reports
In one paragraph

Article in Cureus, 2025. 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
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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

4 authors.

Ikechukwu ChukwuochaNeurology, The Royal Wolverhampton NHS Trust, Wolverhampton, GBR.
Solomon EigbeNeurology, The Royal Wolverhampton NHS Trust, Wolverhampton, GBR.
Di LiangNeurology, The Royal Wolverhampton NHS Trust, Wolverhampton, GBR.
Baig Al-MoyeedNeurology, The Royal Wolverhampton NHS Trust, Wolverhampton, GBR.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL) is an important genetic cause of stroke and vascular dementia, which may also demonstrate variable phenotypic expression. The causative mutation is in the NOTCH3 gene, which maps to chromosome 19 and is largely expressed in the vascular smooth muscle cells of small cerebral blood vessels. The predominant clinical manifestations of this disease include migraines, subcortical ischaemic events, mood disturbances, apathy, and cognitive decline. We herein describe a 46-year-old man who presented to the emergency department with slurred speech, right-sided facial drop, and right lower limb incoordination. Three years before the presentation, he had episodes of right-sided leg stiffness and visual disturbances, which were suspected to be a demyelinating event. Physical examination confirmed increased tone in his lower limbs, worse on the right. His brain MRI showed severe, widespread white matter T2 signal abnormality. The possibility of an adult-onset leucodystrophy was entertained, and the diagnosis of CADASIL was confirmed through genetic testing, which identified a mutation in the NOTCH3 gene. This paper outlines the aetiopathogenesis, clinical presentation, investigations, and management of CADASIL.

Indexed as

cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (cadasil)neuroimaging findingsnotch3 genesmall vessel ischaemic diseasestroke

Identifiers

PMID40486355
PMCPMC12145495

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