Evidence map›Paper›PMID 41888964›Full record

ArticleJournal of medical case reports2026

Multifocal motor neuropathy secondary to gluten intolerance: a case report.

K Haddouali, K Simma, S Bellakhdar, H El Otmani, B El Moutawakil, M A Rafai

Abstract readCase Reports
In one paragraph

Article in Journal of medical case reports, 2026. 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
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

6 authors.

K HaddoualiDepartment of Neurology, Ibn Rochd Hospital, Faculty of Medicine and Pharmacy, Hassan II University, Tarik Ibnou Ziad Street, 20250, Casablanca, Morocco. kamal.haddouali@gmail.com.ORCID http://orcid.org/0009-0002-5656-8669
K SimmaDepartment of Neurology, Ibn Rochd Hospital, Faculty of Medicine and Pharmacy, Hassan II University, Tarik Ibnou Ziad Street, 20250, Casablanca, Morocco.
S BellakhdarDepartment of Neurology, Ibn Rochd Hospital, Faculty of Medicine and Pharmacy, Hassan II University, Tarik Ibnou Ziad Street, 20250, Casablanca, Morocco.
H El OtmaniDepartment of Neurology, Ibn Rochd Hospital, Faculty of Medicine and Pharmacy, Hassan II University, Tarik Ibnou Ziad Street, 20250, Casablanca, Morocco.
B El MoutawakilDepartment of Neurology, Ibn Rochd Hospital, Faculty of Medicine and Pharmacy, Hassan II University, Tarik Ibnou Ziad Street, 20250, Casablanca, Morocco.
M A RafaiDepartment of Neurology, Ibn Rochd Hospital, Faculty of Medicine and Pharmacy, Hassan II University, Tarik Ibnou Ziad Street, 20250, Casablanca, Morocco.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPeripheral nervous system manifestations of gluten sensitivity usually present as distal symmetric axonal polyneuropathy, small fiber neuropathy, or sensory neuropathy, often accompanied by ataxia or painful symptoms. By contrast, motor neuropathies are extremely rare, with only a few cases of multifocal motor neuropathy reported. Notably, the most recent guidelines of the European Society for the Study of Coeliac Disease do not recognize multifocal motor neuropathy as a classical neurological manifestation of gluten-related disorders. The main differential diagnoses include amyotrophic lateral sclerosis and chronic inflammatory demyelinating polyneuropathy. Currently, strict adherence to a gluten-free diet remains the only therapeutic option. Although clinical improvement is not universal, when observed, it strongly supports the causal role of gluten-related neurotoxicity. CASE PRESENTATION: We report the case of a 50-year-old North African man with a history of dermatitis herpetiformis and persistent chronic diarrhea. Over the past 5 years, he developed progressive asymmetric motor weakness. Clinical examination revealed an asymmetric, pure motor, peripheral neurogenic syndrome, confirmed by nerve conduction studies, without evidence of proximal conduction block. Cerebrospinal fluid analysis showed elevated protein levels (0.75 g/L), and serum anti-GD3 IgM antibodies were positive. Brachial plexus magnetic resonance imaging revealed bilateral hypertrophy on T1-weighted sequences, with hyperintensity on short tau inversion recovery sequences but no contrast enhancement. The motor deficit gradually improved after the introduction of a gluten-free diet. The patient also received intravenous immunoglobulin without significant clinical benefit. On the basis of clinical, paraclinical, and follow-up findings, a diagnosis of multifocal motor neuropathy secondary to gluten intolerance was established.

conclusionThis case highlights the importance of considering gluten intolerance as a potential etiology, particularly given the reversible nature of this neuropathy, which can otherwise be misdiagnosed as a more severe condition such as amyotrophic lateral sclerosis. Further studies are needed to better elucidate the pathophysiology of this rare gluten-related neurological phenotype.

Indexed as

Celiac DiseaseDiet, Gluten-FreeGlutensPolyneuropathiesDiagnosis, DifferentialHumansMagnetic Resonance ImagingMaleMiddle AgedNerve Conduction StudiesTreatment OutcomeGlutensGluten-free dietGluten-related disordersMultifocal motor neuropathy

Identifiers

PMID41888964
PMCPMC13141305

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.