Shy-Drager syndrome (Q65222): Difference between revisions
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Shy-Drager é uma forma de atrofia de múltiplos sistemas. A atrofia de múltiplos sistemas (AMS) é uma doença neurodegenerativa esporádica de início na idade adulta (idade média de início de 55 a 58 anos) (duração média da doença de 7 a 9 anos) caracterizada por uma combinação variável de insuficiência autonômica, parkinsonismo e sinais cerebelares. O exame neuropatológico mostra perda neuronal dos núcleos estriatonigral, olivopontocerebelar e autonômico, gliose, palidez de mielina e degeneração axonal. | |||
| description / en | description / en | ||
Shy-Drager is a form of multiple system atrophy. Multiple system atrophy (MSA) is a sporadic, adult onset (mean age of onset 55-58 years) progressive (mean disease duration 7-9 years) neurodegenerative disease characterised by a variable combination of autonomic failure, parkinsonism and cerebellar signs. Neuropathological examination shows striatonigral, olivopontocerebellar and autonomic nuclei neuronal loss, gliosis, myelin pallor and axonal degeneration. | |||
Revision as of 12:56, 14 August 2026
Shy-Drager is a form of multiple system atrophy. Multiple system atrophy (MSA) is a sporadic, adult onset (mean age of onset 55-58 years) progressive (mean disease duration 7-9 years) neurodegenerative disease characterised by a variable combination of autonomic failure, parkinsonism and cerebellar signs. Neuropathological examination shows striatonigral, olivopontocerebellar and autonomic nuclei neuronal loss, gliosis, myelin pallor and axonal degeneration.
| Language | Label | Description | Also known as |
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| default for all languages | ID_859030797 |
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| English | Shy-Drager syndrome |
Shy-Drager is a form of multiple system atrophy. Multiple system atrophy (MSA) is a sporadic, adult onset (mean age of onset 55-58 years) progressive (mean disease duration 7-9 years) neurodegenerative disease characterised by a variable combination of autonomic failure, parkinsonism and cerebellar signs. Neuropathological examination shows striatonigral, olivopontocerebellar and autonomic nuclei neuronal loss, gliosis, myelin pallor and axonal degeneration. |
