Evidence map›Paper›PMID 40688862›Full record

ArticleCureus2025

A Rare Presentation of Wernicke's Encephalopathy With Internuclear Ophthalmoplegia.

Montasir Elmobark, Osama Ahmed, Wisam Ali

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. 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

3 authors.

Montasir ElmobarkGastroenterology, University Hospital of North Tees, Stockton, GBR.
Osama AhmedGeneral Internal Medicine, University Hospital of North Durham, Durham , GBR.
Wisam AliEmergency Department, Best Care Hospital, Khartoum, SDN.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Wernicke's encephalopathy (WE) is a neurological emergency caused by thiamine (vitamin B1) deficiency and classically presents with a triad of confusion, ophthalmoplegia, and ataxia. Although classically associated with chronic alcohol misuse, it may also occur in non-alcoholic individuals due to causes such as persistent vomiting, malnutrition, or gastrointestinal disorders. We present a rare case of WE in a 35-year-old woman who developed internuclear ophthalmoplegia (INO), a highly unusual manifestation in this context. She presented with a one-week history of blurred and double vision, gait unsteadiness, and persistent bilious vomiting, resulting in significant weight loss. Neurological examination revealed right INO with preserved convergence, positive Romberg's sign, and gait ataxia. Imaging revealed fibrous dysplasia of the left temporal bone, but no intracranial abnormalities were suggestive of WE. Based on clinical findings, a clinical diagnosis of WE secondary to persistent vomiting was made. Prompt intravenous thiamine led to a rapid resolution of symptoms. This case underscores the importance of early recognition of atypical WE manifestations, even in the absence of classic imaging findings. Timely thiamine replacement is critical, as delayed or inadequate treatment can result in up to 20% mortality, with approximately 85% of survivors developing Korsakoff's psychosis.

Indexed as

fibrous dysplasia (fd)gait ataxiainternuclear ophthalmoplegiathiamine or vitamin b1 deficiencywernicke’s encephalopathy (we)

Identifiers

PMID40688862
PMCPMC12274564

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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.