MDS Abstracts

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

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  • 2025 International Congress

    Compound Heterozygous SCA17 in a Vietnamese Patient

    C. Knight, L. Hunt, L. Fierro-Cortes, J. Pleen (Kansas City, USA)

    Objective: We seek to report the first instance of Spinocerebellar Ataxia Type 17 (SCA17) in a Vietnamese patient with a compound heterozygous mutation in the…
  • 2025 International Congress

    Hemichorea as an Atypical Manifestation of Hypoglycemia: A Rare Case Report

    Y. Raja Morangkey, A. Tiksnadi, D. Tunjungsari (DKI Jakarta, Indonesia)

    Objective: To present a rare case of hemichorea as a neurological manifestation of hypoglycemia, highlighting the importance of considering metabolic factors in patients with movement…
  • 2025 International Congress

    Adult-Onset Chorea and Psychosis in a 59-Year-Old Man with Elevated Anti-Streptolysin O (aso) Titer

    A. Soriano Ballivian, R. Singh, R. Reshi, U. Verma, Z. Khan, O. Los (Oklahoma City, USA)

    Objective: To review the pathophysiology of neuroimmune disease caused by streptococcal infection using as an example a case of a 59-year-old man with choreiform movements…
  • 2025 International Congress

    Impact of Age of Symptom Onset in Essential Tremor on Cognition in Elderly Individuals

    C. Sangali, G. Pereira, A. Detogni, N. Bruscato, A. Schuh, C. Rieder (Porto Alegre, Brazil)

    Objective: To evaluate the association between age of symptom onset and cognitive function in elderly individuals with Essential Tremor (ET). Background: ET is one of…
  • 2025 International Congress

    Brain Structural Impairment in Spinocerebellar Ataxia Type 6: Not Restricted to the Cerebellum

    B. Massuyama, T. Rezende, M. Junior, O. Barsottini, J. Pedroso (Campinas, Brazil)

    Objective: To characterize the structural brain signature in SCA6 patients. Background: Spinocerebellar ataxias (SCA) refer to a group of autosomal dominant ataxic disorders that result…
  • 2025 International Congress

    A RNF213 truncating variant causes an autosomal dominant disorder with brainstem and basal ganglia lesions and a Huntington-like phenotype

    R. Bovenzi, F. Shen, IJ. Keller Sarmiento, BI. Bustos, L. Kinsley, J. Nichols, D. Krainc, NE. Mencacci (Chicago, USA)

    Objective: To report a novel stop-gain variant in the RNF213 gene in two individuals, a father and son, presenting with variable neurologic presentations and similar…
  • 2025 International Congress

    Seven-year follow-up of clinical and neurophysiological features in essential tremor

    L. Angelini, S. Grandolfo, D. Birreci, D. Costa, M. de Riggi, A. Martini, S. Aloisio, A. Cannavacciuolo, S. Agkun, G. Paparella, M. Bologna (Pozzilli IS, Italy)

    Objective: To prospectively follow-up a sample of Essential Tremor (ET) patients to identify trends in the progression of motor and cognitive symptoms. Background: ET is…
  • 2025 International Congress

    Cardiac Autonomic Dysfunction in Patients with Multiple System Atrophy and Spinocerebellar Ataxia: A Comparative Study and Distinctive Machine Learning Model

    P. Sathirapanya, N. Limotai, C. Limotai, N. Suanprasert, S. Rujirussawarawong, C. Kongkamol, N. Cheetanom (Bangkok, Thailand)

    Objective: To assess the differences of HRV parameters between MSA-C and SCA and their age-matched normal controls and also to use the supervised ML to…
  • 2025 International Congress

    Correlation of the FXTAS Staging System and the FXTAS Rating Scale

    D. Hall, B. Ouyang, M. Tosin (Chicago, USA)

    Objective: To determine correlation between the Fragile X-associated tremor ataxia syndrome (FXTAS) staging system and the FXTAS rating scale Background: FXTAS is an X-linked, neurodegenerative…
  • 2025 International Congress

    Clinical case of Sporadic adult-onset ataxia

    N. Aripova, L. Kenjaeva, B. Bakhtiyor, Y. Nishonova (Tashkent, Uzbekistan)

    Objective: To describe a clinical case of Sporadic adult-onset ataxia(SAOA) Background: Sporadic ataxia in adults is a heterogeneous neurological condition characterized by progressive impairment of…
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