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Severe neuropsychiatric presentation of Wilson's disease
Wilson's disease (WD) is a relatively rare disease of copper metabolism. The diagnosis is often missed initially. The presentation is usually neurologic or hepatic, seen in 40% of patients. Psychiatric presentation of WD is reported in only 15% of patients. We present a 32-year-old patient with...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Medknow Publications
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3136026/ https://www.ncbi.nlm.nih.gov/pubmed/21772656 http://dx.doi.org/10.4103/0019-5545.82556 |
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author | Chakor, Rahul T. Santhosh, N. S. |
author_facet | Chakor, Rahul T. Santhosh, N. S. |
author_sort | Chakor, Rahul T. |
collection | PubMed |
description | Wilson's disease (WD) is a relatively rare disease of copper metabolism. The diagnosis is often missed initially. The presentation is usually neurologic or hepatic, seen in 40% of patients. Psychiatric presentation of WD is reported in only 15% of patients. We present a 32-year-old patient with severe psychiatric manifestations. On examination, he had mild rest and postural tremors and a KF ring was seen. Serum ceruloplasmin was low and 24-hour urinary copper was elevated. The patient responded to penicillamine, lorazepam and quetiapine, and is being followed up. |
format | Online Article Text |
id | pubmed-3136026 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Medknow Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-31360262011-07-19 Severe neuropsychiatric presentation of Wilson's disease Chakor, Rahul T. Santhosh, N. S. Indian J Psychiatry Case Report Wilson's disease (WD) is a relatively rare disease of copper metabolism. The diagnosis is often missed initially. The presentation is usually neurologic or hepatic, seen in 40% of patients. Psychiatric presentation of WD is reported in only 15% of patients. We present a 32-year-old patient with severe psychiatric manifestations. On examination, he had mild rest and postural tremors and a KF ring was seen. Serum ceruloplasmin was low and 24-hour urinary copper was elevated. The patient responded to penicillamine, lorazepam and quetiapine, and is being followed up. Medknow Publications 2011 /pmc/articles/PMC3136026/ /pubmed/21772656 http://dx.doi.org/10.4103/0019-5545.82556 Text en © Indian Journal of Psychiatry http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Chakor, Rahul T. Santhosh, N. S. Severe neuropsychiatric presentation of Wilson's disease |
title | Severe neuropsychiatric presentation of Wilson's disease |
title_full | Severe neuropsychiatric presentation of Wilson's disease |
title_fullStr | Severe neuropsychiatric presentation of Wilson's disease |
title_full_unstemmed | Severe neuropsychiatric presentation of Wilson's disease |
title_short | Severe neuropsychiatric presentation of Wilson's disease |
title_sort | severe neuropsychiatric presentation of wilson's disease |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3136026/ https://www.ncbi.nlm.nih.gov/pubmed/21772656 http://dx.doi.org/10.4103/0019-5545.82556 |
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