Probable MSA |
Sporadic, progressive, adult (>30 years) -onset disease characterized by
AND one of the following predominant motor features
Poorly levodopa-responsive parkinsonism (defined as bradykinesia with rigidity, tremor, or postural instability); OR
A cerebellar syndrome consisting of gait ataxia with cerebellar dysarthria, limb ataxia, or cerebellar oculomotor dysfunction
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Possible MSA |
Sporadic, progressive, adult (>30 years) -onset disease characterized by
Parkinsonism (defined as bradykinesia with rigidity, tremor, or postural instability); OR
A cerebellar syndrome consisting of gait ataxia with cerebellar dysarthria, limb ataxia, or cerebellar oculomotor dysfunction
AND at least one of the following symptoms that suggest autonomic dysfunction including
Urinary urgency
Urinary frequency or incomplete bladder emptying
Erectile dysfunction in males
Significant orthostatic blood pressure drop not meeting the criterion for Probable MSA
AND at least one of the following additional features for MSA-P or MSA-C
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MSA-P or MSA-C
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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 of putamen, middle cerebellar pedunle, pons, or cerebellum
Hypometabolism on FDG-PET in putamen, brainstem, or cerebellum
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MSA-C
Parkinsonism (bradykinesia and rigidity)
Atrophy on MRI of putamen, middle cerebellar peduncle, or pons
Hypometabolism on FDG-PET in putamen
Presynaptic nigrostriatal dopaminergic denervation on SPECT or PET
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