ArticleCureus2026
Multiple System Atrophy-Cerebellar Variant With Absence of Parkinsonian Motor Features.
Article in Cureus, 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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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.
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Authors and funding
4 authors.
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Abstract
Multiple system atrophy (MSA) is a rapidly progressive, multisystem, neurodegenerative disease characterized clinically by varying severity of Parkinsonian features, cerebellar, autonomic, and urogenital dysfunction, and corticospinal disorders. There are two subtypes of MSA - the Cerebellar and Parkinsonian types. The cerebellar subtype (MSA-C) commonly presents with gait ataxia, dysarthria, and coordination deficits; however, the absence of classical Parkinsonian features may delay diagnosis. We report the case of a 52-year-old man who presented with recurrent unexplained falls, progressive gait instability, dysarthria, and cerebellar signs without evidence of rigidity, resting tremor, or bradykinesia. The diagnosis of MSA-C was supported by neuroimaging, which showed significant pontocerebellar atrophy with the distinctive "hot cross bun" sign on MRI. Multiple conditions with similar progressive cerebellar symptoms, like spinocerebellar ataxias, Parkinson's disease, and progressive supranuclear palsy, may show overlapping manifestations. This shows the importance of thorough clinical assessment along with the distinctive neuroimaging in diagnosing MSA-C. In addition, better awareness of the clinical heterogeneity of MSA may facilitate earlier recognition and diagnosis.
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