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February 1926

PARKINSONIAN STATES: CLINICO-PATHOLOGIC STUDIES

Author Affiliations

Professor of Neurology, University of Illinois, College of Medicine; Histologist to Illinois State Psychopathic Institute; Attending Neurologist, Cook County Hospital; Clinical Professor of Neurology, Rush Medical College, University of Chicago; Attending Neurologist, Presbyterian Hospital CHICAGO

From the Pathology Laboratories of the Research and Educational Hospitals, University of Illinois, and of the Illinois State Psychopathic Institute, and the Neurological Service of the Presbyterian Hospital.

Arch NeurPsych. 1926;15(2):218-238. doi:10.1001/archneurpsyc.1926.02200200069005
Abstract

"Parkinsonian states" comprise a large group of morbid conditions possessing a fairly well defined clinical picture—characteristic rigid posture, with expressionless face, retardation of voluntary movements, hypertonia and tremor without signs of pyramidal tract lesion. Here belong Parkinson's disease (paralysis agitans) and so-called postencephalitic parkinsonian syndromes. The similarity between the two is so great that some consider them, clinically as well as pathologically, identical morbid entities. Netter1 maintains that in certain instances Parkinson's disease is caused by the virus of epidemic (lethargic) encephalitis which is responsible for its sequelae ("accidents tardifs"). Souques2 is more emphatic. He looks on both the classic and postencephalitic types as clinical manifestations of one disease—paralysis agitans, the difference being in the degree of the lesion. He asserts that when the encephalitic process in the mesencephalon is slight and "reparable," a parkinsonian syndrome is produced; if the lesion is irreparable, paralysis agitans results. The latter

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