MDS Abstracts

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

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Articles tagged "Ataxia: Genetics"

  • 2018 International Congress

    Comorbid Pediatric Early Onset Ataxia and Dystonia – Is the Cerebellum Involved?

    D. Sival, M. Tijssen, D. Verbeek (Groningen, Netherlands)

    Objective: In children with Early Onset Ataxia (EOA), we aimed to determine the prevalence of comorbid dystonia and to explore the pathogenesis by the shared…
  • 2018 International Congress

    A strategic approach to understand microsatellite repeat loci among Indian spinocerebellar ataxia patients

    V. Suroliya, M. Faruq, A. Srivastava (New Delhi, India)

    Objective: To identify novel unstable tandem nucleotide repeat loci in uncharacterized ataxia patients. Background: Microsatellites like tandem nucleotide repeats are of importance to human genome…
  • 2018 International Congress

    Antisense FMR1 splice variant: A predictor of fragile X-associated tremor/ataxia syndrome

    P. Vittal, S. Pandya, K. Sharp, E. Berry-Kravis, L. Zhou, B. Ouyang, J. Jackson, D. Hall (Winfield, IL, USA)

    Objective: To determine the role of a splice variant of the antisense fragile X mental retardation 1 (ASFMR1) gene, loss of FMR1 AGG interspersions and…
  • 2018 International Congress

    Genotype-phenotype correlations in 104 Uzbekish families with Spinocerebellar ataxias

    F. Rakhimov, Y. Majidova, G. Rakhimbaeva (Tashkent, Uzbekistan)

    Objective: Spinocerebellar ataxias are neurodegenerative disorders involving the cerebellum and its connections. There are more than 30 distinct subtypes, 16 of which are associated with…
  • 2018 International Congress

    Chorea and Ataxia as Manifestations of Xeroderma Pigmentosum: A Case Report

    A. Jocson, K. Ngo, D. Togasaki, B. Fogel (Los Angeles, CA, USA)

    Objective: To report a case of a 51-year-old woman with recurrent basal cell carcinoma, severe photosensitivity, and progressive chorea and ataxia caused by xeroderma pigmentosum…
  • 2018 International Congress

    Multi-tiered Diagnostic Approaches Reveal a High Degree of Genetic Heterogeneity for Hereditary Cerebellar Ataxias: A Retrospective Review of an Australian Cohort

    C. Kang, C. Liang, K. Ahmad, Y. Gu, SF. Siow, J. Colebatch, S. Whyte, K. Ng, P. Cremer, R. Davis, T. Roscioli, M. Cowley, J.S. Park, C. Sue, K. Kumar (Sydney, Australia)

    Objective: A retrospective review of the genetic spectrum in an Australian cohort of hereditary cerebellar ataxia (HCA), as well as evaluating HCA’s testing modalities at…
  • 2018 International Congress

    Daughter’s ataxia reveals father’s genetic Parkinsonism. The first reported case of Spinocerebellar ataxia -15 presenting with levodopa responsive hemi Parkinsonism

    M. Ghaly, C. Wools, A. Evans, E. Storey (St Albans, Australia)

    Objective: A 38 year old Australian florist of Anglo-Celtic origin described two years of difficulty using his right hand with associated sensory disturbance attributed initially…
  • 2018 International Congress

    Clinico-genetic correlation in Indian Spinocerebellar ataxia Type 1 (SCA1) patients

    A. Takkar, I. Ahmed, S. Shakya, A. Srivastava (New Delhi, India)

    Objective: To conduct a clinical and genetic analysis of SCA 1 in Indian population. Background: Spinocerebellar ataxia type1 (SCA1) is a neurodegenerative disease caused by…
  • 2018 International Congress

    Rare ADCY6 variants in two families with cerebellar ataxia, neuropathy and vestibular areflexia syndrome (CANVAS)

    N. Brüggemann, L. Olschewski, V. Tadic, A. Münchau, C. Helmchen, K. Lohmann (Lübeck, Germany)

    Objective: To reveal a genetic cause for a syndrome of combined cerebellar ataxia, neuropathy and vestibular areflexia (CANVAS). Background: CANVAS is a clinically defined neurological…
  • 2018 International Congress

    A new distinct spastic ataxia with hypomyelination: Clinical, neuroimaging and molecular expression of NKX6-2 mutations

    V. Chelban, N. Kaya, M. Alsagob, S. Efthymiou, J. Vandrovcova, D. Lynch, K. Kloth, A. Chirita-Emandi, F. Alkuraya, N. Wood, H. Houlden (London, United Kingdom)

    Objective: To identify the phenotypic, neuroimaging and genotype-phenotype expression of NKX6-2 mutations. Background: Despite advances in genetic testing a large number of hyopomyelinating disorders remain…
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