MDS Abstracts

Abstracts from the International Congress of Parkinson’s and Movement Disorders.

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2026 International Congress » Pediatric Movement Disorders

Meeting: 2026 International Congress

Basal Ganglia Germinoma (BGG) Presenting as Hemidystonia

C. Ryan, R. Patel, S. Younes, M. Chintagumpala, N. Gadgil, M. Parnes (Houston, USA)

Childhood-Onset Parkinsonism with Prominent Pyramidal Signs: A Complex Neurogenetic Phenotype

D. Munoz-Chesta, F. Acuña, M. Troncoso (Santiago, Chile)

Effects of Manual Therapy on Hand Dexterity in Children Aged 4–8 Years: A Prospective Interventional Study

TV. Voloshyn (TRUSKAVETS, Ukraine)

Expanding the Childhood Spectrum of Dentatorubral–pallidoluysian Atrophy: Neuropsychiatric and Motor Phenotypes in Four Siblings

M. Siegel, I. Malaty, A. Ramirez-Zamora (Gainesville, USA)

Feasibility of Remote Identification of Catatonia Across Different Motor Presentations

N. Kadubandi, A. Elshourbagy, A. Tasmiya, M. van Emdeboas, R. Aydin, A. Epstein, R. Guo, L. Smith, N. Li, J. Barnett, J. Brasic (Baltimore, USA)

From Clinical Patterns to Symptom-specific Functional Networks in Dyskinetic Cerebral Palsy

AL. Almeida Marcelino, B. Al-Fatly, L. de Pol, M. Tuncer, NM. Wilpert, A. Tietze, C. Werner, A. Saryyeva, M. San Luciano, L. Timmermann, A. Schnitzler, J. Krauss, P. Starr, A. Kaindl, A. Koy, A. Buizer, A. Kühn (Berlin, Germany)

Functional Improvement Following Early GPi-DBS for Moderate-Stage Atypical KMT2B Dystonia: A Case Report in a 13-Year-Old Girl

Z. Sclavont, V. Leclercq, C. Vilain, S. Schuind, F. Supiot, N. Deconinck, P. van Gyseghem (Brussels, Belgium)

Genotype-Phenotype Correlations in KCNMA1 Channelopathy: A Comparative Analysis of Gain-of-Function and Loss-of-Function Variants in a Korean Cohort and Literature Review

JM. Kim, S. Lee, SY. Kim, J. Moon, JH. Chae (Seoul, Republic of Korea)

IncobotulinumtoxinA for the Treatment of Lower Limb Spasticity in Children and Adolescents with Cerebral Palsy Evaluation of Lower Limb IncobotulinumtoxinA Efficacy (ELLIE)

I. Makedonska (Dnipro, Ukraine)

Integrating Multidisciplinary, Family-Centered Care to Optimize Functional Outcomes in Children with Cerebral Palsy.

T. Voloshyn (TRUSKAVETS, Ukraine)

Movement Disorder Phenotypes and Etiological Associations in Genetic Early-Onset Ataxias: A Pediatric Cohort Study

F. Dridi, H. Klaa, M. Ben Hafsa, Z. Miladi, T. Ben Younes, A. Zioudi, M. Jamoussi, H. Benrhouma, I. Kraoua (Tunis, Tunisia)

Movement Disorder Spectrum and Neurological Outcomes in Children with Neuronal Ceroid Lipofuscinosis

A. Saini, S. Vaidya (chandigarh, India)

Multi-Omics Biomarker Discovery in Friedreich’s Ataxia Cardiomyopathy

F. Siddiqui, T. Keller, C. Koehring, G. Upadhyay, B. Higgins, T. Zesiewicz, K. Kim, G. Halade, A. Patel, T. Mcdonald (Tampa, USA)

Neurological disease progression in adults with ataxia telangiectasia – a longitudinal study

AE. Hensiek, L. Bottolo, MY. Tiet, E. Harrison, H. Biggs, E. Ashby, C. Olympio, N. Everett, R. Horvath (Cambridge, United Kingdom)

Paroxismal Torticollis Revealing Cervical disc Calcifications in a Child About a Case

C. Boukadir (Benaknoun; Algiers, Algeria)

Pelizaeus Merzbacher like disease (PMLD): Neuroradiological Phenotyping

K. Shah, M. Shah (Mumbai, India)

Plasma Phospho-Tau217 and Neuromelanin-Sensitive MRI as Candidate Biomarkers in Beta-Propeller Protein-Associated Neurodegeneration

JH. Lee, YS. Kim (Yangsan, Republic of Korea)

Presence of Common Psychiatric Diagnoses Did Not Impact the Efficacy or Safety of Ecopipam in Individuals With Tourette Syndrome

J. Mcguire, J. Flatt, G. Karkanias, F. Munschauer, T. Cunniff, S. Wanaski, E. Greenberg (Baltimore, USA)

Receptor Selectivity Profile and Clinical Significance of Ecopipam and Its Metabolites as a Potential Therapy for Tourette Syndrome

S. Wanaski, V. Schmith, G. Karkanias, T. Cunniff (Chicago, USA)

Safety and Effect of Ecopipam During the First 8 Weeks of Treatment for Tourette Syndrome: A Post Hoc Analysis

K. Tomczak, T. Katz, J. Flatt, G. Karkanias, S. Wanaski, T. Cunniff, D. Gilbert (Boston, USA)

SCN8A-Related Disorders: Expanding the Movement Disorder Phenotype Through a Case Report and Literature Review

R. Alkhodair, H. Alfaris, S. Yoganathan, C. Gorodetsky (Toronto, Canada)

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