Highly Effective, Short‐Latency Responses to Pallidal Stimulation in Axial Dystonia Supports Early Deep Brain Stimulation

BACKGROUND: Axial dystonia is a rare form of adult-onset focal dystonia. The majority of cases are idiopathic, however a similar phenotype can be seen in monogenic dystonias and tardive syndromes. Management of axial dystonia can be challenging, and most cases are typically refractory to pharmacotherapy and botulinum toxin injections. CASES: We describe three cases of axial-predominant dystonia, two idiopathic and one with a monogenic etiology, each demonstrating an early and excellent response to GPi DBS. LITERATURE REVIEW: We conducted a narrative review of the existing literature on axial dystonia, which remains limited to case reports and small series, with no large cohort studies to guide evidence-based management. CONCLUSIONS: Consistent with limited previous reports and the three cases presented, our findings suggest that GPi DBS offers favorable outcomes in refractory AD regardless of underlying pathological substrate and should be considered early in disease course.

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Publication Details

Journal
Movement Disorders Clinical Practice
Published
2026-09-29
DOI
https://doi.org/10.1002/mdc3.70845
Primary Topic
Neurological disorders and treatments
Type
article
Field-Weighted Citation Impact
0.00
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article

Highly Effective, Short‐Latency Responses to Pallidal Stimulation in Axial Dystonia Supports Early Deep Brain Stimulation

Erlick A C Pereira, Moran Catherine, Eoghan Donlon, Maeve Bradley et al.
Movement Disorders Clinical Practice
Neurological disorders and treatments
article

Highly Effective, Short‐Latency Responses to Pallidal Stimulation in Axial Dystonia Supports Early Deep Brain Stimulation

Erlick A C Pereira, Moran Catherine, Eoghan Donlon, Maeve Bradley, J Horan, Federica Ruggieri, Richard A. Walsh, Timothy Lynch, Conor Fearon, Marie Kelly, Elaine Reynolds
article en

Abstract

BACKGROUND: Axial dystonia is a rare form of adult-onset focal dystonia. The majority of cases are idiopathic, however a similar phenotype can be seen in monogenic dystonias and tardive syndromes. Management of axial dystonia can be challenging, and most cases are typically refractory to pharmacotherapy and botulinum toxin injections. CASES: We describe three cases of axial-predominant dystonia, two idiopathic and one with a monogenic etiology, each demonstrating an early and excellent response to GPi DBS. LITERATURE REVIEW: We conducted a narrative review of the existing literature on axial dystonia, which remains limited to case reports and small series, with no large cohort studies to guide evidence-based management. CONCLUSIONS: Consistent with limited previous reports and the three cases presented, our findings suggest that GPi DBS offers favorable outcomes in refractory AD regardless of underlying pathological substrate and should be considered early in disease course.

Movement Disorders Clinical Practice
University College Dublin (IE), Royal College of Surgeons in Ireland (IE), St George's, University of London (GB), Trinity College Dublin (IE), London Clinic (GB), Beaumont Hospital (IE), Mater Misericordiae University Hospital (IE)
Good health and well-being
Openalex Percentile: Top 12%
Neurological disorders and treatments
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