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... > Nervous System Diseases > Central Nervous System Diseases > Brain Diseases > Cerebellar Diseases > Spinocerebellar Degenerations > Myoclonic Cerebellar Dyssynergia
Nervous System Diseases > Central Nervous System Diseases > Spinal Cord Diseases > Spinocerebellar Degenerations > Myoclonic Cerebellar Dyssynergia
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Heredodegenerative Disorders, Nervous System > Spinocerebellar Degenerations > Myoclonic Cerebellar Dyssynergia
Nervous System Diseases > Neurodegenerative Diseases > Heredodegenerative Disorders, Nervous System > Spinocerebellar Degenerations > Myoclonic Cerebellar Dyssynergia

Término preferido

Myoclonic Cerebellar Dyssynergia  

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Tipo

  • mesh:Descriptor

Definición

  • A condition marked by progressive CEREBELLAR ATAXIA combined with MYOCLONUS usually presenting in the third decade of life or later. Additional clinical features may include generalized and focal SEIZURES, spasticity, and DYSKINESIAS. Autosomal recessive and autosomal dominant patterns of inheritance have been reported. Pathologically, the dentate nucleus and brachium conjunctivum of the CEREBELLUM are atrophic, with variable involvement of the spinal cord, cerebellar cortex, and basal ganglia. (From Joynt, Clinical Neurology, 1991, Ch37, pp60-1)

Concepto genérico

Etiquetas alternativas

  • Cerebellar Dyssynergia
  • Dentate Cerebellar Ataxia
  • Dentate Cerebellar Atrophy
  • Dentate Nucleus Syndrome, Ramsay Hunt
  • Dyssynergia Cerebellaris Myoclonica
  • Dyssynergia Cerebellaris Progressiva
  • Ramsay Hunt Cerebellar Syndrome
  • Ramsay Hunt Dentate Syndrome

En otras lenguas

URI

http://data.loterre.fr/ark:/67375/JVR-S38P0XRH-K

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