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Hyperemesis Gravidarum Complicated by Wernicke’s Encephalopathy: A Case Report
Wernicke’s encephalopathy (WE) is a rare neurologic disease caused by a deficiency in thiamine (B1). It is characterized by features of altered mental status, cerebellar dysfunction, and ophthalmoplegia. Most often, cases are attributed to long-term alcohol use; however, rarer causes have been descr...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cureus
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9089282/ https://www.ncbi.nlm.nih.gov/pubmed/35547424 http://dx.doi.org/10.7759/cureus.24009 |
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author | Punal, Natalie Prasad, Supritha Haque, Afsara Lei, Justin Santiago, Gaia |
author_facet | Punal, Natalie Prasad, Supritha Haque, Afsara Lei, Justin Santiago, Gaia |
author_sort | Punal, Natalie |
collection | PubMed |
description | Wernicke’s encephalopathy (WE) is a rare neurologic disease caused by a deficiency in thiamine (B1). It is characterized by features of altered mental status, cerebellar dysfunction, and ophthalmoplegia. Most often, cases are attributed to long-term alcohol use; however, rarer causes have been described in the literature. In this article, we describe a case of WE caused by hyperemesis gravidarum in a 19-year-old female with no known medical history. |
format | Online Article Text |
id | pubmed-9089282 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Cureus |
record_format | MEDLINE/PubMed |
spelling | pubmed-90892822022-05-10 Hyperemesis Gravidarum Complicated by Wernicke’s Encephalopathy: A Case Report Punal, Natalie Prasad, Supritha Haque, Afsara Lei, Justin Santiago, Gaia Cureus Internal Medicine Wernicke’s encephalopathy (WE) is a rare neurologic disease caused by a deficiency in thiamine (B1). It is characterized by features of altered mental status, cerebellar dysfunction, and ophthalmoplegia. Most often, cases are attributed to long-term alcohol use; however, rarer causes have been described in the literature. In this article, we describe a case of WE caused by hyperemesis gravidarum in a 19-year-old female with no known medical history. Cureus 2022-04-10 /pmc/articles/PMC9089282/ /pubmed/35547424 http://dx.doi.org/10.7759/cureus.24009 Text en Copyright © 2022, Punal et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Internal Medicine Punal, Natalie Prasad, Supritha Haque, Afsara Lei, Justin Santiago, Gaia Hyperemesis Gravidarum Complicated by Wernicke’s Encephalopathy: A Case Report |
title | Hyperemesis Gravidarum Complicated by Wernicke’s Encephalopathy: A Case Report |
title_full | Hyperemesis Gravidarum Complicated by Wernicke’s Encephalopathy: A Case Report |
title_fullStr | Hyperemesis Gravidarum Complicated by Wernicke’s Encephalopathy: A Case Report |
title_full_unstemmed | Hyperemesis Gravidarum Complicated by Wernicke’s Encephalopathy: A Case Report |
title_short | Hyperemesis Gravidarum Complicated by Wernicke’s Encephalopathy: A Case Report |
title_sort | hyperemesis gravidarum complicated by wernicke’s encephalopathy: a case report |
topic | Internal Medicine |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9089282/ https://www.ncbi.nlm.nih.gov/pubmed/35547424 http://dx.doi.org/10.7759/cureus.24009 |
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