MDS Abstracts

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

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  • 2024 International Congress

    eHealth – an Opportunity for personalized Care? – Healthcare Professionals’ Technology Acceptance in the Care of Parkinson’s Patients

    J. Stuempel, J. Hohn, V. Fleckenstein, K. Steidel, C. Münte, D. Pedrosa (Marburg, Germany)

    Objective: To examine how eHealth may improve personalized care for people with Parkinson's disease (PwPD) from the perspective of healthcare professionals (HCPs). Background: Parkinson's disease…
  • 2024 International Congress

    How does the PPP2R2B mutation alter neuronal cytoskeletal structure in SCA12

    A. Ganguly, B. Reddy, J. Rungta, S. Choudhury, R. Pal, H. Kumar, S. Chattarji (Kolkata, India)

    Objective: To study the effect of the PPP2R2B mutation on human induced pluripotent stem cell (iPSC) derived neurons in SCA12 patients. Background: SCA12 is an…
  • 2024 International Congress

    Pulmonary Dysfunction in Friedreich’s Ataxia (FRDA)

    T. Zesiewicz, T. Vu, A. Patel, T. Mcdonald, Y. Huang, Y. Zhao, L. Campbell, L. Evans, D. Mohan, C. Gooch, K. Calero (Tampa, USA)

    Objective: We sought to characterize pulmonary function in FRDA and identify disease variables that may contribute to dysfunction. Background: FRDA is a neurodegenerative disease that causes…
  • 2024 International Congress

    Substantia Nigra Degeneration In Spinocerebellar Ataxia 2 And 7 Using Neuromelanin-Sensitive Imaging

    L. Chougar, G. Coarelli, FX. Lejeune, R. Gaurav, P. Ziegner, A. Durr, S. Lehéricy (PARIS, France)

    Objective: To assess substantia nigra pars compacta (SN) degeneration in SCA type 2 and 7 using neuromelanin-sensitive MRI Background: Spinocerebellar ataxias (SCA) are often associated…
  • 2024 International Congress

    Clinico-radiological and genetic profile of patients with Ataxia with Oculomotor apraxia type-2 (AOA2)- A case series from India

    M. Chandarana, B. Tilva, A. Agarwal, D. Garg (Ahmedabad, India)

    Objective: To delineate clinical, radiological and genetic profile of patients with ataxia with oculomotor apraxia type-2 (AOA2) in Indian cohort. Background: AOA2 is a relatively…
  • 2024 International Congress

    A study on the phenomenological analysis of Spinocerebellar Ataxia type 12 revealing a dystonic imprint

    A. Mukherjee, S. Pandey (Faridabad, India)

    Objective: To assess the presence and distribution of dystonia in spinocerebellar ataxia type 12 (SCA12). Background: SCA12, commonly seen in the Agarwal community in India,…
  • 2024 International Congress

    Chorea Acanthocytosis Misdiagnosed as Functional Movement Disorder

    A. Crutchfield, N. Reddy, A. Ahmed, M. Lotia (Orlando, USA)

    Objective: To highlight the importance of genetic testing when the clinical symptoms of Chorea Acanthocytosis (ChAc) are misdiagnosed as functional movement disorder (FMD). Background: ChAc…
  • 2024 International Congress

    Motor and Quality of Life Outcomes of Deep Brain Stimulation for Pediatric Dystonia – CHILD-DBS Registry

    W K. Lim, C. Gorodetsky, G. Ibrahim, K. Mithani, S. Breitbart, A. Leblanc-Millar, A. Fasano (Toronto, Canada)

    Objective: To evaluate the motor and quality of life (QoL) outcomes of deep brain stimulation for pediatric dystonia with the following parameters: BFMDRS, total number…
  • 2024 International Congress

    Intrafamilial phenotypic variability of DYT-ANO3: Analyzing 14 affected members with a novel variant

    J. Ganguly, N. Sarmah, A. Rawool, H. Kumar (Kolkata, India)

    Objective: Delineation of phenotypic diversity of DYT-ANO3 in a large tribal family of Indian origin. Background: DYT-ANO3 (DYT24) is a rare cause of autosomal dominant…
  • 2024 International Congress

    The Yips in Golf: Is it a Task-Specific Dystonia ?

    E. van Wensen (Apeldoorn, Netherlands)

    Objective: The aim of this study is to classify the phenomenology of the Yips in Golf and investigate what underlies this anomalous movement by answering…
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