Evidence map›Paper›PMID 42518048›Full record

ArticleCerebellum (London, England)2026

Gluten Ataxia in Children and Adolescents.

Ala Fadilah, Daniel Connolly, Marios Hadjivassiliou, Graeme Wild, Santosh R Mordekar

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Article in Cerebellum (London, England), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Ala FadilahDepartment of Paediatric Neurology, Sheffield Children's Hospital NHS Foundation Trust Ryegate Children's Centre, Sheffield, S10 5DD, UK.
Daniel ConnollyDepartment of Radiology, Royal Hallamshire Hospital, Glossop Road, Sheffield, S10 2JF, United Kingdom.
Marios HadjivassiliouDepartment of Neurology, Floor M, Sheffield Teaching Hospitals NHS Foundation Trust, Sheffield, United Kingdom.
Graeme WildDepartment of Neurology, Floor M, Sheffield Teaching Hospitals NHS Foundation Trust, Sheffield, United Kingdom.
Santosh R MordekarDepartment of Paediatric Neurology, Sheffield Children's Hospital NHS Foundation Trust Ryegate Children's Centre, Sheffield, S10 5DD, UK. santosh.mordekar@nhs.net.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Neurological manifestations of gluten sensitivity (GS) with gluten ataxia (GA) are well-recognised in adults. We present our experience in children and adolescents (C/A) seen with suspected GS, mainly GA, over a 5-year period. Retrospective case note analysis was performed on clinical, serological andneuroimaging data of 20 C/A seen in our specialist ataxia referral centre withsuspected NGS. 14 female and 6 male C/A (range: 6-15 years, median: 12.5 years) were referred to our specialist ataxia clinic with suspected GS. All 20 patients had motor coordination/balance difficulties with ataxia. Headaches were present in 12/20 C/A (60%), sensory neuropathic symptoms in 6/20 C/a (30%), postural dizziness in 6/20 (30%). 8/20 C/A (40%) had pre-existing autism spectrum disorder (ASD). Family history of GS/GA/Coeliac disease was present in 10/20 C/A (50%). Serological abnormalities were present in all 20 CYP, with raised antibodies: antigliadin in 15/20 (75%), transglutaminase-6 in 12/20 (60%), transglutaminase-2 in 7/20 (35%), and endomysial in 4/20 (20%). MR Spectroscopy of the cerebellum showed a reduced N-acetylaspartate: Creatine (NAA/Cr) ratio in 14/20 (70%). 18/20 (90%) received a gluten-free diet (GFD). 13/18 (72%) of C/A reported improvement of symptoms on GFD. We suggest considering GS as a differential diagnosis in the presence of motor coordination difficulties with abnormal MRS of the cerebellum and raised antigliadin and/or transglutaminase-6 antibodies. Early diagnosis of GS is important, as it is a treatable cause of childhood ataxia.Further follow-up will help in defining the natural history and GS in C/A.

Indexed as

AtaxiaCeliac DiseaseGlutensAdolescentAutoantibodiesChildFemaleHumansMaleRetrospective StudiesTransglutaminasesAutoantibodiesGlutensTransglutaminasesAtaxiaChildrenGluten sensitivity

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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.