Spectrum of Movement Disorders in Early‐Onset Hereditary Spastic Paraplegia: A Study of 428 Cases

Movement disorders are common, genotype-specific, and clinically impactful features of childhood-onset HSP. Routine screening and genotype-tailored management of movement disorders, especially dystonia, may improve functional outcomes and quality of life. © 2025 International Parkinson and Movement Disorder Society.

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Publication Details

Journal
Movement Disorders
Published
2025-12-02
DOI
https://doi.org/10.1002/mds.70141
Primary Topic
Hereditary Neurological Disorders
Type
article
Field-Weighted Citation Impact
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article

Spectrum of Movement Disorders in Early‐Onset Hereditary Spastic Paraplegia: A Study of 428 Cases

Kathryn Yang, Sally E. Carty, Marcondes C. França, Amy Tam et al.
Movement Disorders
Hereditary Neurological Disorders
article

Spectrum of Movement Disorders in Early‐Onset Hereditary Spastic Paraplegia: A Study of 428 Cases

Kathryn Yang, Sally E. Carty, Marcondes C. França, Amy Tam, Darius Ebrahimi‐Fakhari, Zainab Zaman, Carelis González‐Salazar, Julian E. Alecu, Matthias Kieslich, Filippo Maria Santorelli, Katerina Bernardi, Vicente Quiroz, Luca Schierbaum, Dario Resch, Habibah A.P. Agianda, Nicole Battaglia, Joshua Rong
article en

Abstract

Movement disorders are common, genotype-specific, and clinically impactful features of childhood-onset HSP. Routine screening and genotype-tailored management of movement disorders, especially dystonia, may improve functional outcomes and quality of life. © 2025 International Parkinson and Movement Disorder Society.

Movement DisordersVol. 41(3)
Goethe University Frankfurt (DE), Boston Children's Hospital (US), Harvard University (US), Universidade Estadual de Campinas (UNICAMP) (BR), Fondazione Stella Maris (IT), University Hospital Frankfurt (DE), Hospital de Clínicas da Unicamp (BR)
Openalex Percentile: Top 59%
Hereditary Neurological Disorders
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