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Multiple System Atrophy, Cerebellar type
URI:
https://gptkb.org/entity/Multiple_System_Atrophy,_Cerebellar_type
GPTKB entity
Statements (43)
Predicate
Object
gptkbp:instanceOf
neurodegenerative disease
gptkbp:abbreviation
gptkb:MSA-C
gptkbp:affects
gptkb:basal_ganglia
gptkb:cerebellum
autonomic nervous system
gptkbp:associatedWith
oligodendroglial cytoplasmic inclusions
gptkbp:cause
unknown
gptkbp:characterizedBy
autonomic dysfunction
parkinsonism
cerebellar ataxia
gptkbp:diagnosedBy
clinical evaluation
MRI brain
gptkbp:differentialDiagnosis
gptkb:Parkinson's_disease
gptkb:progressive_supranuclear_palsy
spinocerebellar ataxia
gptkbp:firstDescribed
1960s
gptkbp:gender
slightly more common in men
gptkbp:hasEpidemiology
rare
https://www.w3.org/2000/01/rdf-schema#label
Multiple System Atrophy, Cerebellar type
gptkbp:ICD-10_code
G23.2
gptkbp:medianSurvival
6-10 years
gptkbp:MeSH_ID
D020754
gptkbp:MRI_finding
hot cross bun sign
gptkbp:notableFeature
lack of response to levodopa
gptkbp:OMIM
146500
gptkbp:onset
adult
50-60 years
gptkbp:pathology
alpha-synuclein accumulation
gptkbp:prevalence
3-5 per 100,000
gptkbp:prognosis
poor
gptkbp:progression
gptkb:fire
gptkbp:riskFactor
unknown
gptkbp:subspecies
gptkb:Multiple_System_Atrophy
gptkbp:symptom
gptkb:orthostatic_hypotension
gait disturbance
dysphagia
urinary incontinence
dysarthria
gptkbp:treatment
supportive care
physical therapy
medications for symptoms
gptkbp:bfsParent
gptkb:MSA-C
gptkbp:bfsLayer
8