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Dictionary » Spinocerebellar ataxia
 

Spinocerebellar ataxia

Introduction: Spinocerebellar ataxia

Description of Spinocerebellar ataxia

Spinocerebellar ataxia (medical condition): A condition characterised by a failure of muscle...more »

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Spinocerebellar Ataxia:
  »Introduction: Spinocerebellar Ataxia
  »Symptoms of Spinocerebellar Ataxia

Spinocerebellar ataxia: A group of dominantly inherited, predominately late-onset, cerebellar ataxias which have been divided into multiple subtypes based on clinical features and genetic mapping. Progressive ataxia is a central feature of these conditions, and in certain subtypes POLYNEUROPATHY; DYSARTHRIA; visual loss; and other disorders may develop. (From Joynt, Clinical Neurology, 1997, Ch65, pp 12-17; J Neuropathol Exp Neurol 1998 Jun;57(6):531-43)
Source: Diseases Database

Spinocerebellar ataxia: Related Topics

These medical condition or symptom topics may be relevant to medical information for Spinocerebellar ataxia:

Spinocerebellar ataxia as a Disease

Spinocerebellar ataxia (medical condition): See Spinocerebellar Ataxia (disease information).
  »Introduction: Spinocerebellar Ataxia
  »Symptoms of Spinocerebellar Ataxia

Spinocerebellar ataxia: Related Diseases

Spinocerebellar ataxia: Spinocerebellar ataxia is listed as a type of (or associated with) the following medical conditions in our database:

Spinocerebellar ataxia: Article Excerpts

Persons with spinocerebellar ataxia, of which there are several types, experience a degeneration of the spinal cord...(Source: Genes and Disease by the National Center for Biotechnology)

More information on medical condition: Spinocerebellar Ataxia:

Spinocerebellar ataxia: Related Disease Topics

These medical disease topics may be related to Spinocerebellar ataxia:

  • inherited ataxia
  • hereditary ataxia
  • progressive limb and gait ataxia
  • dysarthria
  • loss of joint position and vibration senses
  • absent tendon reflexes in the legs

External links related to: Spinocerebellar ataxia

Source: Diseases Database

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