Evidence map›Paper›PMID 41503320›Full record

ArticleCureus2025

Early Sensory-Predominant Guillain-Barré Syndrome With Normal Cerebrospinal Fluid and MRI Findings: A Diagnostic Challenge.

Salah Riyadh, Robert Knopp

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

2 authors.

Salah RiyadhEmergency Department, Pikeville Medical Center, Pikeville, USA.
Robert KnoppEmergency Department, Pikeville Medical Center, Pikeville, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Guillain-Barré syndrome (GBS) is an acute, immune-mediated polyneuropathy that classically presents with progressive, symmetric weakness and areflexia following a preceding infection. However, early or atypical presentations may lack the hallmark diagnostic features, such as elevated cerebrospinal fluid (CSF) protein or abnormal magnetic resonance imaging (MRI) findings, creating a diagnostic challenge. We present the case of a 46-year-old woman who developed progressive distal paresthesias, gait instability, perioral numbness, hoarseness, and later right foot-drop following a viral-like illness. Initial evaluation revealed normal CSF protein levels, an unremarkable MRI of the brain and spine, and preserved strength, leading to diagnostic uncertainty. Despite these findings, the clinical pattern raised suspicion for early sensory-predominant GBS, and intravenous immunoglobulin therapy was initiated with subsequent clinical improvement. This case underscores the importance of maintaining high clinical suspicion for GBS in patients with compatible symptoms, even in the absence of classical diagnostic findings, to ensure timely intervention and prevent progression.

Indexed as

acute inflammatory demyelinating polyradiculoneuropathycerebrospinal fluiddiagnostic challengeguillain‒barre syndromeintravenous immunoglobulinnerve conduction studiesperoneal neuropathysensory neuropathy

Identifiers

PMID41503320
PMCPMC12769224

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.