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Anesthetic considerations in Leigh disease: Case report and literature review
Leigh disease is an extremely rare disorder, characterized by a progressive neurodegenerative course, with subacute necrotizing encephalomyelopathy. It usually presents in infancy with developmental delay, seizures, dysarthria, and ataxia. These patients may also develop episodes of lactic acidosis...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3385266/ https://www.ncbi.nlm.nih.gov/pubmed/22754450 http://dx.doi.org/10.4103/1658-354X.97037 |
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author | Terkawi, Abdullah Sulieman Wani, Tariq M. Al-Shuaibi, Khalid M. Tobias, Joseph D. |
author_facet | Terkawi, Abdullah Sulieman Wani, Tariq M. Al-Shuaibi, Khalid M. Tobias, Joseph D. |
author_sort | Terkawi, Abdullah Sulieman |
collection | PubMed |
description | Leigh disease is an extremely rare disorder, characterized by a progressive neurodegenerative course, with subacute necrotizing encephalomyelopathy. It usually presents in infancy with developmental delay, seizures, dysarthria, and ataxia. These patients may also develop episodes of lactic acidosis that usually lead to respiratory failure and death. Due to the rarity of the condition, the most appropriate anesthetic plan remains unclear. We present a patient with Leigh disease, who required general anesthesia. The pathogenesis of the disease is discussed and previous reports of perioperative care from the literature are reviewed. |
format | Online Article Text |
id | pubmed-3385266 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-33852662012-07-02 Anesthetic considerations in Leigh disease: Case report and literature review Terkawi, Abdullah Sulieman Wani, Tariq M. Al-Shuaibi, Khalid M. Tobias, Joseph D. Saudi J Anaesth Case Report Leigh disease is an extremely rare disorder, characterized by a progressive neurodegenerative course, with subacute necrotizing encephalomyelopathy. It usually presents in infancy with developmental delay, seizures, dysarthria, and ataxia. These patients may also develop episodes of lactic acidosis that usually lead to respiratory failure and death. Due to the rarity of the condition, the most appropriate anesthetic plan remains unclear. We present a patient with Leigh disease, who required general anesthesia. The pathogenesis of the disease is discussed and previous reports of perioperative care from the literature are reviewed. Medknow Publications & Media Pvt Ltd 2012 /pmc/articles/PMC3385266/ /pubmed/22754450 http://dx.doi.org/10.4103/1658-354X.97037 Text en Copyright: © Saudi Journal of Anaesthesia 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 Terkawi, Abdullah Sulieman Wani, Tariq M. Al-Shuaibi, Khalid M. Tobias, Joseph D. Anesthetic considerations in Leigh disease: Case report and literature review |
title | Anesthetic considerations in Leigh disease: Case report and literature review |
title_full | Anesthetic considerations in Leigh disease: Case report and literature review |
title_fullStr | Anesthetic considerations in Leigh disease: Case report and literature review |
title_full_unstemmed | Anesthetic considerations in Leigh disease: Case report and literature review |
title_short | Anesthetic considerations in Leigh disease: Case report and literature review |
title_sort | anesthetic considerations in leigh disease: case report and literature review |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3385266/ https://www.ncbi.nlm.nih.gov/pubmed/22754450 http://dx.doi.org/10.4103/1658-354X.97037 |
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