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Gitelman syndrome: a rare life‐threatening case of hypokalemic paralysis mimicking Guillain–Barré syndrome during pregnancy and review of the literature
In rare cases, patients with Gitelman syndrome may present with hypokalemic paralysis mimicking Guillain–Barré syndrome. The severity of resultant symptoms may be life‐threatening. Controversial drugs such as aldactone, amiloride, and eplerenone should be used in this situation despite the lack of s...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5628240/ https://www.ncbi.nlm.nih.gov/pubmed/29026553 http://dx.doi.org/10.1002/ccr3.1122 |
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author | Elkoundi, Abdelghafour Kartite, Noureddine Bensghir, Mustapha Doghmi, Nawfal Lalaoui, Salim Jaafar |
author_facet | Elkoundi, Abdelghafour Kartite, Noureddine Bensghir, Mustapha Doghmi, Nawfal Lalaoui, Salim Jaafar |
author_sort | Elkoundi, Abdelghafour |
collection | PubMed |
description | In rare cases, patients with Gitelman syndrome may present with hypokalemic paralysis mimicking Guillain–Barré syndrome. The severity of resultant symptoms may be life‐threatening. Controversial drugs such as aldactone, amiloride, and eplerenone should be used in this situation despite the lack of safety data. |
format | Online Article Text |
id | pubmed-5628240 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-56282402017-10-12 Gitelman syndrome: a rare life‐threatening case of hypokalemic paralysis mimicking Guillain–Barré syndrome during pregnancy and review of the literature Elkoundi, Abdelghafour Kartite, Noureddine Bensghir, Mustapha Doghmi, Nawfal Lalaoui, Salim Jaafar Clin Case Rep Case Reports In rare cases, patients with Gitelman syndrome may present with hypokalemic paralysis mimicking Guillain–Barré syndrome. The severity of resultant symptoms may be life‐threatening. Controversial drugs such as aldactone, amiloride, and eplerenone should be used in this situation despite the lack of safety data. John Wiley and Sons Inc. 2017-08-17 /pmc/articles/PMC5628240/ /pubmed/29026553 http://dx.doi.org/10.1002/ccr3.1122 Text en © 2017 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Reports Elkoundi, Abdelghafour Kartite, Noureddine Bensghir, Mustapha Doghmi, Nawfal Lalaoui, Salim Jaafar Gitelman syndrome: a rare life‐threatening case of hypokalemic paralysis mimicking Guillain–Barré syndrome during pregnancy and review of the literature |
title | Gitelman syndrome: a rare life‐threatening case of hypokalemic paralysis mimicking Guillain–Barré syndrome during pregnancy and review of the literature |
title_full | Gitelman syndrome: a rare life‐threatening case of hypokalemic paralysis mimicking Guillain–Barré syndrome during pregnancy and review of the literature |
title_fullStr | Gitelman syndrome: a rare life‐threatening case of hypokalemic paralysis mimicking Guillain–Barré syndrome during pregnancy and review of the literature |
title_full_unstemmed | Gitelman syndrome: a rare life‐threatening case of hypokalemic paralysis mimicking Guillain–Barré syndrome during pregnancy and review of the literature |
title_short | Gitelman syndrome: a rare life‐threatening case of hypokalemic paralysis mimicking Guillain–Barré syndrome during pregnancy and review of the literature |
title_sort | gitelman syndrome: a rare life‐threatening case of hypokalemic paralysis mimicking guillain–barré syndrome during pregnancy and review of the literature |
topic | Case Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5628240/ https://www.ncbi.nlm.nih.gov/pubmed/29026553 http://dx.doi.org/10.1002/ccr3.1122 |
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