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Topiramate-induced hyperammonemic encephalopathy in a patient with mental retardation: A case report and review of the literature
Hyperammonemia is an uncommon side effect of topiramate (TPM) that has only been reported when it is used as an adjunct to valproate. We report a patient with mental retardation who developed reversible encephalopathy from TPM. Ammonia level was monitored during the course of TPM treatment. This pat...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4576360/ https://www.ncbi.nlm.nih.gov/pubmed/26543812 http://dx.doi.org/10.1016/j.ebcr.2014.09.001 |
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author | Tantikittichaikul, Sahawat Johnson, Justine Laengvejkal, Pavis DeToledo, John |
author_facet | Tantikittichaikul, Sahawat Johnson, Justine Laengvejkal, Pavis DeToledo, John |
author_sort | Tantikittichaikul, Sahawat |
collection | PubMed |
description | Hyperammonemia is an uncommon side effect of topiramate (TPM) that has only been reported when it is used as an adjunct to valproate. We report a patient with mental retardation who developed reversible encephalopathy from TPM. Ammonia level was monitored during the course of TPM treatment. This patient had recurring, reversible elevations in serum ammonia levels that coincided with the administration of TPM. To our knowledge, symptomatic hyperammonemia has not been reported to occur with TPM monotherapy. |
format | Online Article Text |
id | pubmed-4576360 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-45763602015-11-05 Topiramate-induced hyperammonemic encephalopathy in a patient with mental retardation: A case report and review of the literature Tantikittichaikul, Sahawat Johnson, Justine Laengvejkal, Pavis DeToledo, John Epilepsy Behav Case Rep Case Report Hyperammonemia is an uncommon side effect of topiramate (TPM) that has only been reported when it is used as an adjunct to valproate. We report a patient with mental retardation who developed reversible encephalopathy from TPM. Ammonia level was monitored during the course of TPM treatment. This patient had recurring, reversible elevations in serum ammonia levels that coincided with the administration of TPM. To our knowledge, symptomatic hyperammonemia has not been reported to occur with TPM monotherapy. Elsevier 2015-09-15 /pmc/articles/PMC4576360/ /pubmed/26543812 http://dx.doi.org/10.1016/j.ebcr.2014.09.001 Text en © 2014 Published by Elsevier Inc. http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/3.0/). |
spellingShingle | Case Report Tantikittichaikul, Sahawat Johnson, Justine Laengvejkal, Pavis DeToledo, John Topiramate-induced hyperammonemic encephalopathy in a patient with mental retardation: A case report and review of the literature |
title | Topiramate-induced hyperammonemic encephalopathy in a patient with mental retardation: A case report and review of the literature |
title_full | Topiramate-induced hyperammonemic encephalopathy in a patient with mental retardation: A case report and review of the literature |
title_fullStr | Topiramate-induced hyperammonemic encephalopathy in a patient with mental retardation: A case report and review of the literature |
title_full_unstemmed | Topiramate-induced hyperammonemic encephalopathy in a patient with mental retardation: A case report and review of the literature |
title_short | Topiramate-induced hyperammonemic encephalopathy in a patient with mental retardation: A case report and review of the literature |
title_sort | topiramate-induced hyperammonemic encephalopathy in a patient with mental retardation: a case report and review of the literature |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4576360/ https://www.ncbi.nlm.nih.gov/pubmed/26543812 http://dx.doi.org/10.1016/j.ebcr.2014.09.001 |
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