Evidence map›Paper›PMID 41138027›Full record

SynthesisActa neurologica Belgica2026

Spectrum of movement disorders in Japanese encephalitis: a systematic review of case reports, case series, and cohort studies.

Ravindra Kumar Garg, Shweta Pandey, Raza Abbas Mahdi, Sanjay Singhal, Neeraj Kumar

Abstract readSystematic ReviewReview
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In one paragraph

Synthesis in Acta neurologica Belgica, 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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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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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

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5 · Who and what money

Authors and funding

5 authors.

Ravindra Kumar GargDepartment of Neurology Era's Lucknow Medical College & Hospital, Era University, Lucknow, 226003, India. garg50@yahoo.com.ORCID http://orcid.org/0000-0003-0044-7083
Shweta PandeyDepartment of Neurology, King George's Medical University, Lucknow, 226003, India.
Raza Abbas MahdiDepartment of Nuclear Medicine, Postgraduate Institute of Medical Education and Research Chandigarh, Chandigarh, 160012, India.
Sanjay SinghalDepartment of Pulmonary Medicine, Dr. Ram Manohar Lohia Institute of Medical Sciences, Lucknow, India.
Neeraj KumarDepartment of Neurology, King George's Medical University, Lucknow, 226003, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMovement disorders are common, disabling sequelae of Japanese encephalitis (JE) survivors yet remain poorly characterized. This review synthesizes their epidemiology, clinical spectrum, radiological correlates and outcomes to inform early diagnosis and treatment.

methodsWe searched PubMed, Scopus, Embase and Google Scholar data bases for reports of JE with subsequent movement disorders. We included case reports, case series and cohort studies. Extracted data on demographics, timing and type of movement disorder, magnetic resonance imaging findings, treatment and follow-up outcomes were recorded.

resultsIn this review of 72 isolated JE cases, the mean age was 20.8 years (range < 1-66), with 39 males (54.2%). Most cases (60%) were from India. The most frequent movement disorder was parkinsonism (18, 25%), followed by rigidity (13, 18.1%), bradykinesia (8, 11.1%), and hypomimia (7, 9.7%). Dystonia occurred in 28 (38.9%), including generalized (6.7%), oromandibular (2.2%), and opisthotonus (4.5%). Neuropsychiatric features were noted in 22 (30.6%), bulbar-autonomic signs in 14 (19.4%), and long-term sequelae in 11 (15.3%). Abnormal cerebrospinal fluid was found in 44 (61.1%), and bilateral thalamic hyperintensities on MRI in 49 (68.1%). Symptomatic treatment was given in 15 (20.8%) and immunotherapy in 7 (9.7%). Outcomes included partial improvement in 20 (27.8%), complete in 12 (16.7%), and death in 1 (1.4%). Two Indian retrospective cohorts (n = 209, n = 50) showed similar spectrum of movement disorders with predominant thalamic-basal ganglia involvement.

conclusionsMovement disorders following JE are common, predominantly parkinsonism and dystonia, often with bilateral thalamic involvement and variable recovery.

Indexed as

Encephalitis, JapaneseMovement DisordersAdolescentAdultChildChild, PreschoolCohort StudiesFemaleHumansMaleMiddle AgedYoung AdultDystoniaJapanese encephalitisMovement disordersNeuroimagingParkinsonism

Identifiers

PMID41138027

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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.