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Catatonia: A rare presentation of Wilson's disease
Wilson's disease (WD) or hepatolenticular degeneration is a rare inherited disorder of copper metabolism affecting both the liver and the central nervous system. Psychiatric manifestations may precede neurological signs in the early stages of WD, but catatonia is a rare presentation. Here, we r...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer - Medknow
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8611575/ https://www.ncbi.nlm.nih.gov/pubmed/34908723 http://dx.doi.org/10.4103/0972-6748.328843 |
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author | Davis, Supriya Chag, Jwalant Rohatgi, Salesh Chaudhury, Suprakash Saldanha, Daniel |
author_facet | Davis, Supriya Chag, Jwalant Rohatgi, Salesh Chaudhury, Suprakash Saldanha, Daniel |
author_sort | Davis, Supriya |
collection | PubMed |
description | Wilson's disease (WD) or hepatolenticular degeneration is a rare inherited disorder of copper metabolism affecting both the liver and the central nervous system. Psychiatric manifestations may precede neurological signs in the early stages of WD, but catatonia is a rare presentation. Here, we report a case of an 18-year-old girl who presented to the psychiatry outpatient department with catatonia. She was subsequently diagnosed to have WD. Her symptoms improved on treatment with trientine, trihexyphenidyl, zinc acetate, and benzodiazepine. |
format | Online Article Text |
id | pubmed-8611575 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Wolters Kluwer - Medknow |
record_format | MEDLINE/PubMed |
spelling | pubmed-86115752021-12-13 Catatonia: A rare presentation of Wilson's disease Davis, Supriya Chag, Jwalant Rohatgi, Salesh Chaudhury, Suprakash Saldanha, Daniel Ind Psychiatry J Case Report Wilson's disease (WD) or hepatolenticular degeneration is a rare inherited disorder of copper metabolism affecting both the liver and the central nervous system. Psychiatric manifestations may precede neurological signs in the early stages of WD, but catatonia is a rare presentation. Here, we report a case of an 18-year-old girl who presented to the psychiatry outpatient department with catatonia. She was subsequently diagnosed to have WD. Her symptoms improved on treatment with trientine, trihexyphenidyl, zinc acetate, and benzodiazepine. Wolters Kluwer - Medknow 2021-10 2021-10-22 /pmc/articles/PMC8611575/ /pubmed/34908723 http://dx.doi.org/10.4103/0972-6748.328843 Text en Copyright: © 2021 Industrial Psychiatry Journal https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms. |
spellingShingle | Case Report Davis, Supriya Chag, Jwalant Rohatgi, Salesh Chaudhury, Suprakash Saldanha, Daniel Catatonia: A rare presentation of Wilson's disease |
title | Catatonia: A rare presentation of Wilson's disease |
title_full | Catatonia: A rare presentation of Wilson's disease |
title_fullStr | Catatonia: A rare presentation of Wilson's disease |
title_full_unstemmed | Catatonia: A rare presentation of Wilson's disease |
title_short | Catatonia: A rare presentation of Wilson's disease |
title_sort | catatonia: a rare presentation of wilson's disease |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8611575/ https://www.ncbi.nlm.nih.gov/pubmed/34908723 http://dx.doi.org/10.4103/0972-6748.328843 |
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