Extrapyramidal and movement disorders

Description

postencephalitic Parkinson disease: Parkinsonism following encephalitis, historically seen as a sequella of encephalitis lethargica (Von Economo Encephalitis). The early age of onset, the rapid progression of symptoms followed by stabilization, and the presence of a variety of other neurological disorders (e.g., sociopathic behavior; TICS; MUSCLE SPASMS; oculogyric crises; hyperphagia; and bizarre movements) distinguish this condition from primary PARKINSON DISEASE. Pathologic features include neuronal loss and gliosis concentrated in the MESENCEPHALON; SUBTHALAMUS; and HYPOTHALAMUS. (From Adams et al., Principles of Neurology, 6th ed, p754)

Data source
FinnGen phenocode G6_XTRAPYR
Include G6_PARKINSON, G6_PARKSCND, G6_BASDEGENOTH, G6_DYSTON, G6_XTRAPYROTH
Level in the ICD-hierarchy 2
First defined in version DF2
Ontology
DOID 14332
GWAS catalog 1001402
MESH D010301
SNOMED CT 19972008

Key figures

Sex All Female Male
Number of individuals 2862 1500 1362
Unadjusted prevalence (%) 2.16 2.0 2.37
Mean age at first event (years) 60.53 59.52 61.64
Median number of events / individual 2 2 2

Clinical metrics

Sex All Female Male
Recurrence within 6 months (%) 55.56 55.13 56.02
Case fatality at 5-years (%) 7.9 7.07 8.81

Associations