Creutzfeldt-Jakob disease with mixed transcortical aphasia: Insights into echolalia

0Citations
Citations of this article
6Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

Aphasia is a common manifestation of Creutzfeldt-Jakob disease (CJD), and investigation of the linguistic disorders of CJD patients may provide insights into the neurobiological mechanisms of language and aphasia. We report an autopsy-confirmed case of CJD in which the presenting symptom was change in language abilities. The patient ultimately evidenced mixed transcortical aphasia (MTA) with echolalia. Disruption of frontal-subcortical circuits with environmental dependency accounts for the symptoms in MTA, including intact repetition and echolalia. Observation in this patient and a review of the literature suggest that frontal-subcortical circuit dysfunction may contribute to the syndrome of echolalia. This hypothesis offers an alternative explanation to “isolation” of the speech area as the cause of MTA. © 1994 Rapid Communications of Oxford Ltd.

Cite

CITATION STYLE

APA

McPherson, S. E., Kuratani, J. D., Cummings, J. L., Shih, J., Mischel, P. S., & Vinters, H. V. (1994). Creutzfeldt-Jakob disease with mixed transcortical aphasia: Insights into echolalia. Behavioural Neurology, 7(3–4), 197–203. https://doi.org/10.1155/1994/601201

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free