ArticleCerebellum (London, England)2026
Rare and Atypical Manifestations of ARSACS-A Report of Two Cases.
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.
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.
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Authors and funding
11 authors.
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Abstract
ARSACS (Autosomal Recessive Spastic Ataxia of Charlevoix Saguenay) is a neurodegenerative disease resulting from mutation in the SACS gene. Although it classically presents with the triad of ataxia, spasticity and peripheral neuropathy, it is known to have variability in clinical presentation, progression and severity. We report two atypical cases of ARSACS (both without spasticity) and one presenting with focal epilepsy (another rare clinical manifestation).
Indexed as
Identifiers
41941018What Socratic holds
Registered trials
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 Socratic graph.