Evidence map›Paper›PMID 42220968›Full record

SynthesisTremor and other hyperkinetic movements (New York, N.Y.)2026

Spectrum of Dystonia in Spinocerebellar Ataxia.

Siva Roja Yellaturi, Adreesh Mukherjee, Sanjay Pandey

Abstract readSystematic Review
In one paragraph

Synthesis in Tremor and other hyperkinetic movements (New York, N.Y.), 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

3 authors.

Siva Roja YellaturiDepartment of Neurology and Stroke Medicine, Amrita Institute of Medical Sciences, Mata Amritanandamayi Marg Sector 88, Faridabad, Delhi National Capital Region, India.
Adreesh MukherjeeDepartment of Neurology, Bangur Institute of Neurosciences, Institute of Post Graduate Medical Education and Research, Kolkata, India.
Sanjay PandeyDepartment of Neurology and Stroke Medicine, Amrita Institute of Medical Sciences, Mata Amritanandamayi Marg Sector 88, Faridabad, Delhi National Capital Region, India.ORCID 0000-0003-1771-9137

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Spinocerebellar ataxias (SCAs) are a diverse group of inherited disorders characterized by progressive cerebellar dysfunction. Beyond the classic ataxic features, dystonia is an important manifestation across both common and uncommon SCA subtypes. The complete clinical spectrum, pathophysiology, and treatment of dystonia in SCA remain incompletely understood. Objectives: This review aims to summarize the current literature on dystonia in SCAs, outlining its prevalence, clinical presentations, underlying mechanisms, and therapeutic strategies. Methods: The authors conducted a systematic literature review in PubMed (up to October 2025) with various search terms related to dystonia and spinocerebellar ataxia, including specific SCA types. Full text articles were included in the review based on clinical relevance. Results: Dystonia has been observed in the common SCAs such as SCA1, 2, and 3, as well as several of the rarer SCA types. While focal dystonias such as cervical dystonia and task-specific dystonia (writer's cramp) are frequent manifestations, generalized dystonias are also documented. Dystonia may follow the ataxia, or can be the presenting symptom itself. Dystonia in SCA results from dysfunction in the interconnected brain networks primarily involving the cerebellum, basal ganglia, thalamus, and sensorimotor cortex. An altered dopaminergic signalling may be present as well. Treatment responses to levodopa, anticholinergics, botulinum toxin, and deep brain stimulation vary widely, underscoring the need for individualized therapeutic approaches. Conclusions: Recognizing dystonia as a part of the SCA spectrum is important for timely diagnosis and management. Further studies are required to elucidate the mechanisms and explore the targeted interventions.

Indexed as

DystoniaSpinocerebellar AtaxiasHumansCerebellumDystoniaManagementPathophysiologySpinocerebellar Ataxia

Identifiers

PMID42220968
PMCPMC13220735

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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.