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... > Nervous System Diseases > Central Nervous System Diseases > Brain Diseases > Cerebellar Diseases > Cerebellar Ataxia > Spinocerebellar Ataxias
... > Nervous System Diseases > Neurologic Manifestations > Dyskinesias > Ataxia > Cerebellar Ataxia > Spinocerebellar Ataxias
... > Pathological Conditions, Signs and Symptoms > Signs and Symptoms > Neurologic Manifestations > Dyskinesias > Ataxia > Cerebellar Ataxia > Spinocerebellar Ataxias
... > Nervous System Diseases > Central Nervous System Diseases > Movement Disorders > Dyskinesias > Ataxia > Cerebellar Ataxia > Spinocerebellar Ataxias
... > Nervous System Diseases > Central Nervous System Diseases > Brain Diseases > Cerebellar Diseases > Spinocerebellar Degenerations > Spinocerebellar Ataxias
Nervous System Diseases > Central Nervous System Diseases > Spinal Cord Diseases > Spinocerebellar Degenerations > Spinocerebellar Ataxias
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Heredodegenerative Disorders, Nervous System > Spinocerebellar Degenerations > Spinocerebellar Ataxias
Nervous System Diseases > Neurodegenerative Diseases > Heredodegenerative Disorders, Nervous System > Spinocerebellar Degenerations > Spinocerebellar Ataxias

Preferred term

Spinocerebellar Ataxias  

Type

  • mesh:Descriptor

Definition

  • A group of 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) A group of dominantly inherited, predominatly 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)

Broader concept

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Entry terms

  • Spinocerebellar Atrophies

Allowable Qualifier(s)

In other languages

  • Ataxies spinocérébelleuses

    French

  • Ataxies cérébelleuses autosomiques dominantes
  • Ataxies spino-cérébelleuses
  • Ataxies spino-cérébelleuses dominantes
  • Ataxies spino-cérébelleuses héréditaires dominantes
  • Ataxies spinocérébelleuses autosomiques dominantes
  • Ataxies spinocérébelleuses dominantes
  • Ataxies spinocérébelleuses héréditaires dominantes
  • SCA (SpinoCerebellar Ataxia)

URI

http://data.loterre.fr/ark:/67375/JVR-GPCH3BKZ-5

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