MDS Abstracts

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

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  • 2024 International Congress

    Evaluating Adaptive Devices to Assist Eating in Essential Tremor Patients: A Comparative Analysis

    K. Adabi, W. Ondo (Houston, USA)

    Objective: To evaluate the effectiveness of six adaptive devices to mitigate tremor impact while eating in patients with essential tremor (ET), compared to a standard…
  • 2024 International Congress

    Haptics’ use in extended reality environments for Parkinson disease: A systematic review

    L. Ali, C. Lella, G. Giuliano, R. Di Fuccio (Napoli, Italy)

    Objective: This systematic review aims to identify how haptics in extended reality (XR) are used for patients with Parkinson disease (PD) and their outcome in…
  • 2024 International Congress

    The Use of Biometric Feedback Devices for Stratification of Deep Brain Stimulation (DBS) Eligibility and Treatment Response in Parkinson Disease

    E. Kolesnick, H. Ooi, M. Rashid, K. Pain, H. Sarva, A. Deik (New York, USA)

    Objective: To review the literature on digital biomarkers’ role in DBS candidacy assessment and treatment response in people with Parkinson Disease (PwP). Background: Visit frequency…
  • 2024 International Congress

    Comparative Analysis of GAITRite and Moticon Digital Insoles for Gait Assessment in Parkinson’s Disease Patients Before and After Levodopa Administration

    R. Acosta, B. Kuyani, S. Stuart, A. Avbersek, P. Rai, S. Mishra, K. Kwei, D. Hall, N. Desai, S. Hamon, J. Urbanek, R. Alaj, O. Harari, M. Wipperman, O. Levy (Tarrytown, USA)

    Objective: Parkinson’s disease (PD) is characterized by gait impairments, impacting patient mobility and quality of life. This study compares a reference gait measurement system, GAITRite (GR) against digital…
  • 2024 International Congress

    Variant Ataxia Telangiectasia: A Novel ATM Gene Mutation With Disabling Tremor and Response to Deep Brain Stimulation

    S. Giri Ravindran, A. Rajput, N. Noyes (Saskatoon, Canada)

    Objective: We describe a patient with a novel ATM gene variant presenting with tremor, neuropathy, and late-onset ataxia. Background: Ataxia Telangiectasia (AT) is an autosomal…
  • 2024 International Congress

    Clinical and Genetic Profile of Spinocerebellar Ataxias in a Tunisian Cohort

    M S. Majoul, R. Zouari, A. Kalfat, R. Amouri, D. Ben Mohamed, M Z. Saied, F. Nabli, S. Ben Sassi (Tunis, Tunisia)

    Objective: Our aim was to determine the clinical, genetic and radiological characteristics of spinocerebellar ataxias (SCA) in a Tunisian cohort. Background: SCA is a heterogenous…
  • 2024 International Congress

    Alterations in the Daily Living Gait and Mobility during the Day and Night among Individuals with Cerebellar Ataxia, SCA3: An Exploratory Study

    P. Ponger, A. Solomon, M. Brozgol, E. Gazit, J. Hausdorff (Tel Aviv, Israel)

    Objective: In this pilot study, we aimed to examine step counts and daily living physical activity, confirm findings regarding gait variability, explore changes in nighttime…
  • 2024 International Congress

    Superficial siderosis; a case review

    ANM. Afifi, L. Satke, E. čecháková (Olomouc, Czech Republic)

    Objective: To highlight an often overlooked cause of ataxia with hearing impairment. Background: Superficial siderosis (SS) of the nervous system is caused by chronic hemosiderin…
  • 2024 International Congress

    A Novel Mutation of NKX2-1 Gene: A Rare Presentation of Chorea

    BC. Ari, S. Canbek, G. Kenangil (ISTANBUL, Turkey)

    Objective: NKX2-1-related disorders encompass a spectrum extending from benign hereditary chorea (BHC) to choreoathetosis, hypothyroidism, neonatal respiratory distress. The prevalence of chorea remains undetermined, albeit…
  • 2024 International Congress

    Choreoacanthocytosis: The First Genetically Confirmed Cases From Algeria

    Y. Mecheri, S. Talbi, A. Rezigue, M. Zouzou, BS. Fekraoui, F. Serradj, A. M'Zahem (Constantine, Algeria)

    Objective: Here we describe for the first time two unrelated cases of genetically confirmed Choreoacanthocytosis from Algeria. Background: Choreoacanthocytosis is a rare and severe inherited…
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