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Additional features of possible multiple system atrophy

Additional features of possible multiple system atrophy
Possible MSA-P or MSA-C
Babinski sign with hyperreflexia
Stridor
Possible MSA-P*
Rapidly progressive parkinsonism
Poor response to levodopa
Postural instability within 3 years of motor onset
Gait ataxia, cerebellar dysarthria, limb ataxia, or cerebellar oculomotor dysfunction
Dysphagia within 5 years of motor onset
Atrophy on MRI scan of putamen, middle cerebellar peduncle, pons, or cerebellum
Hypometabolism on FDG-PET scan in putamen, brainstem, or cerebellum
Possible MSA-C
Parkinsonism (bradykinesia and rigidity)
Atrophy on MRI of putamen, middle cerebellar peduncle, or pons
Hypometabolism on FDG-PET scan in putamen
Presynaptic nigrostriatal dopaminergic denervation on SPECT or PET scan
MSA-P: multiple system atrophy with predominant parkinsonism; MSA-C: multiple system atrophy with predominant cerebellar ataxia; MRI: magnetic resonance imaging; FDG: [18F]fluorodeoxyglucose; PET: positron emission tomography; SPECT: single-photon emission computed tomography.
* In the absence of clinically evident ataxia in a patient with parkinsonian features, these features can point to the diagnosis of MSA-P rather than Parkinson disease.
¶ In the absence of parkinsonian features in a patient with cerebellar ataxia, these features can point to the diagnosis of MSA-C rather than other causes of progressive ataxia in adults.
From: Gilman S, Wenning GK, Low PA, et al. Second consensus statement on the diagnosis of multiple system atrophy. Neurology 2008; 71:670. DOI: 10.1212/01.wnl.0000324625.00404.15. Copyright © 2008 American Academy of Neurology. Reproduced with permission from Wolters Kluwer Health. Unauthorized reproduction of this material is prohibited.
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