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Wernicke Korsakoff syndrome in a teenage female as a complication of COVID‐19
Wernicke encephalitis (WE) is usually associated with alcohol use disorder and caused by a deficiency in thiamine. Classic findings include confusion, ataxia, and ophthalmoplegia. This case is a unique presentation of WE in a 14‐year‐old female related to prior coronavirus disease infection. She had...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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John Wiley and Sons Inc.
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9051863/ https://www.ncbi.nlm.nih.gov/pubmed/35505931 http://dx.doi.org/10.1002/emp2.12735 |
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author | Skok, Hannah Jabour, Joseph Betcher, Joseph |
author_facet | Skok, Hannah Jabour, Joseph Betcher, Joseph |
author_sort | Skok, Hannah |
collection | PubMed |
description | Wernicke encephalitis (WE) is usually associated with alcohol use disorder and caused by a deficiency in thiamine. Classic findings include confusion, ataxia, and ophthalmoplegia. This case is a unique presentation of WE in a 14‐year‐old female related to prior coronavirus disease infection. She had persistent dysgeusia and developed thiamine deficiency. She presented with confusion, ataxia, and changes in speech. She had a prolonged hospitalization but was discharged to an inpatient rehab facility with persistent symptoms. It is prudent to include thiamine deficiency in the differential for patients with any symptoms of WE and a history of nutritional deficiency. |
format | Online Article Text |
id | pubmed-9051863 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-90518632022-05-02 Wernicke Korsakoff syndrome in a teenage female as a complication of COVID‐19 Skok, Hannah Jabour, Joseph Betcher, Joseph J Am Coll Emerg Physicians Open General Medicine Wernicke encephalitis (WE) is usually associated with alcohol use disorder and caused by a deficiency in thiamine. Classic findings include confusion, ataxia, and ophthalmoplegia. This case is a unique presentation of WE in a 14‐year‐old female related to prior coronavirus disease infection. She had persistent dysgeusia and developed thiamine deficiency. She presented with confusion, ataxia, and changes in speech. She had a prolonged hospitalization but was discharged to an inpatient rehab facility with persistent symptoms. It is prudent to include thiamine deficiency in the differential for patients with any symptoms of WE and a history of nutritional deficiency. John Wiley and Sons Inc. 2022-04-29 /pmc/articles/PMC9051863/ /pubmed/35505931 http://dx.doi.org/10.1002/emp2.12735 Text en © 2022 The Authors. JACEP Open published by Wiley Periodicals LLC on behalf of American College of Emergency Physicians. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | General Medicine Skok, Hannah Jabour, Joseph Betcher, Joseph Wernicke Korsakoff syndrome in a teenage female as a complication of COVID‐19 |
title | Wernicke Korsakoff syndrome in a teenage female as a complication of COVID‐19 |
title_full | Wernicke Korsakoff syndrome in a teenage female as a complication of COVID‐19 |
title_fullStr | Wernicke Korsakoff syndrome in a teenage female as a complication of COVID‐19 |
title_full_unstemmed | Wernicke Korsakoff syndrome in a teenage female as a complication of COVID‐19 |
title_short | Wernicke Korsakoff syndrome in a teenage female as a complication of COVID‐19 |
title_sort | wernicke korsakoff syndrome in a teenage female as a complication of covid‐19 |
topic | General Medicine |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9051863/ https://www.ncbi.nlm.nih.gov/pubmed/35505931 http://dx.doi.org/10.1002/emp2.12735 |
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