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... > Nervous System Diseases > Central Nervous System Diseases > Brain Diseases > Basal Ganglia Diseases > Multiple System Atrophy > Striatonigral Degeneration
Nervous System Diseases > Central Nervous System Diseases > Movement Disorders > Multiple System Atrophy > Striatonigral Degeneration
Nervous System Diseases > Autonomic Nervous System Diseases > Primary Dysautonomias > Multiple System Atrophy > Striatonigral Degeneration
... > Nutritional and Metabolic Diseases > Metabolic Diseases > Proteostasis Deficiencies > Synucleinopathies > Multiple System Atrophy > Striatonigral Degeneration
Nervous System Diseases > Neurodegenerative Diseases > Synucleinopathies > Multiple System Atrophy > Striatonigral Degeneration

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Striatonigral Degeneration  

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Tipo

  • mesh:Descriptor

Definición

  • A sporadic neurodegenerative disease with onset in middle-age characterized clinically by Parkinsonian features (e.g., MUSCLE RIGIDITY; HYPOKINESIA; stooped posture) and HYPOTENSION. This condition is considered a clinical variant of MULTIPLE SYSTEM ATROPHY. Pathologic features include a prominent loss of neurons in the zona compacta of the SUBSTANTIA NIGRA and PUTAMEN. (From Adams et al., Principles of Neurology, 6th ed, p1075-6)

Concepto genérico

Conceptos relacionados

Etiquetas alternativas

  • Striatonigral Atrophy

En otras lenguas

  • Dégénerescence striatonigrique

    francés

  • Dégénérescence de la voie nigro-striée
  • Dégénerescence de la voie nigrostriée
  • Dégénérescence nigrostriée
  • Dégénérescence striato-nigrique
  • Dégénérescence striatonigrale
  • DSN (Dégénérescence StriatoNigrique)

URI

http://data.loterre.fr/ark:/67375/JVR-QQ6D1XXP-9

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