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Spinocerebellar ataxia type 6 (brain MRI)

Midline sagittal brain MRI of a patient with spinocerebellar ataxia type 6 demonstrating cerebellar atrophy without pontine or medullary atrophy. (Contributed by Dr. Michael Oh.)

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Associated Disorders

  • Acute cerebellar ataxia in children
  • Autosomal dominant hereditary ataxias
  • Celiac disease (Neurologic complications of celiac disease)
  • Cerebellar astrocytoma
  • Chiari malformation
  • Fragile X-associated tremor/ataxia syndrome
  • Hereditary spastic paraplegia
  • Many other specific disorders
  • Medulloblastoma
  • Nondominant hereditary ataxias
  • Nonparaneoplastic autoimmune cerebellar diseases
  • Paraneoplastic cerebellar degeneration
  • Pontocerebellar hypoplasias
  • Sensory neuropathies associated with anti-GD1b ganglioside antibodies
  • Spinocerebellar ataxias
  • Structural lesions of the cerebellum
  • Wilson disease