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Title of Journal: Cerebellum

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Abbravation: The Cerebellum

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Springer US

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DOI

10.1016/0038-1098(73)90473-0

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1473-4230

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NonAtaxic Presenting Symptoms of Dominant Ataxias

Authors: Elsdon Storey
Publish Date: 2015/09/16
Volume: 15, Issue: 1, Pages: 26-29
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Abstract

While the onset of a dominantly inherited ataxia is typically taken to be the onset of gait ataxia a wide range of other symptoms related to central and/or peripheral nervous system impairment or even to nonneurological involvement can be the presenting feature Knowledge of these is fairly robust for the commonest spinocerebellar ataxias SCAs 1 2 3 and 6 and for those where a striking nonataxic presentation is the norm SCAs 7 and 12 but the literature is potentially misleading in the rarer dominant ataxias This review summarises what is currently known of these nonataxic presentations and outlines and explains the difficulties associated with determining nonataxic presentations of dominant ataxias The relevant literature was surveyed including systematic reviews where available and case reports Nonataxic presentations of dominant ataxias are classified by symptom

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Other Papers In This Journal:
  1. Cerebellum: from Fundamentals to Translational Approaches. The Seventh International Symposium of the Society for Research on the Cerebellum
  2. Cerebellar Contribution to Anger Recognition Deficits in Huntington’s Disease
  3. T-Type Calcium Channel as a New Therapeutic Target for Tremor
  4. Compartmentation of the Cerebellar Cortex in the Naked Mole-Rat ( Heterocephalus glaber )
  5. Behavioural Significance of Cerebellar Modules
  6. An fMRI Investigation of Cerebellar Function During Verbal Working Memory in Methadone Maintenance Patients
  7. Neurofilament Heavy Chain Expression Reveals a Unique Parasagittal Stripe Topography in the Mouse Cerebellum
  8. Regional Cerebellar Volumes Predict Functional Outcome in Children with Cerebellar Malformations
  9. Predictive Motor Timing Performance Dissociates Between Early Diseases of the Cerebellum and Parkinson's Disease
  10. A Cerebellar Framework for Predictive Coding and Homeostatic Regulation in Depressive Disorder
  11. Spinal Cord Atrophy Correlates with Disability in Friedreich’s Ataxia
  12. High Serum GFAP Levels in SCA3/MJD May Not Correlate with Disease Progression
  13. High Serum GFAP Levels in SCA3/MJD May Not Correlate with Disease Progression
  14. Recessive Spinocerebellar Ataxia with Paroxysmal Cough Attacks: A Report of Five Cases
  15. Cerebellum and Personality Traits
  16. Development of External Surfaces of Human Cerebellar Lobes in the Fetal Period
  17. Friedreich's Ataxia Causes Redistribution of Iron, Copper, and Zinc in the Dentate Nucleus
  18. Increased Catabolic State in Spinocerebellar Ataxia Type 1 Patients
  19. Mild Clinical and Biochemical Phenotype in Two Patients with PMM2-CDG (Congenital Disorder of Glycosylation Ia)
  20. Cerebellar Function in Developmental Dyslexia
  21. Glutamate Dysfunction Associated with Developmental Cerebellar Damage: Relevance to Autism Spectrum Disorders
  22. Asymmetries in Cerebellar Plasticity and Motor Learning
  23. Clinical Manifestations of Cerebellar Infarction According to Specific Lobular Involvement
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