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Psychosomatic Medicine, Vol 57, Issue 2 202-204, Copyright © 1995 by American Psychosomatic Society
ORIGINAL ARTICLES |
LV McDonald and CR Lake
Department of Psychiatry and Behavioral Sciences, University of Kansas Medical Center, Kansas City 66160-7341, USA.
Wilson's disease is a rare genetic disorder involving the liver and brain, with onset frequently in adolescence. Psychiatric symptoms are often the first manifestation of the disease and can obscure the diagnosis. Chelation therapy can reverse the fatal outcome of untreated patients, so early detection is critically important. This paper describes an adolescent with Wilson's disease who, after initiation of penicillamine therapy, developed florid psychosis that improved as copper levels were decreased and that did not require use of neuroleptic medication.
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E. CHRONI, N. P. LEKKA, E. TSIBRI, A. ECONOMOU, and C. PASCHALIS Acute, Progressive Akinetic-Rigid Syndrome Induced by Neuroleptics in a Case of Wilson's Disease J Neuropsychiatry Clin Neurosci, November 1, 2001; 13(4): 531 - 532. [Full Text] [PDF] |
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A R. o. t. ANPA Committee on Research, E. C. Lauterbach, J. L. Cummings, J. Duffy, C. E. Coffey, D. Kaufer, M. Lovell, P. Malloy, A. Reeve, D. R. Royall, et al. Neuropsychiatric Correlates and Treatment of Lenticulostriatal Diseases: A Review of the Literature and Overview of Research Opportunities in Huntington's, Wilson's, and Fahr's Diseases J Neuropsychiatry Clin Neurosci, August 1, 1998; 10(3): 249 - 266. [Abstract] [Full Text] |
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