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Double jeopardy: long QT3 and Brugada syndromes
Mutations in the SCN5A gene are linked to both the long QT syndrome 3 and Brugada syndrome with few reports describing an overlapping phenotype. We present a unique case and discuss clinical considerations of a patient concurrently exhibiting such conditions with genetic analysis confirming an SCN5A...
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/PMC5538234/ https://www.ncbi.nlm.nih.gov/pubmed/28781849 http://dx.doi.org/10.1002/ccr3.1064 |
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author | Sandhu, Amneet Borne, Ryan T. Mam, Chandara Bunch, T. Jared Aleong, Ryan G. |
author_facet | Sandhu, Amneet Borne, Ryan T. Mam, Chandara Bunch, T. Jared Aleong, Ryan G. |
author_sort | Sandhu, Amneet |
collection | PubMed |
description | Mutations in the SCN5A gene are linked to both the long QT syndrome 3 and Brugada syndrome with few reports describing an overlapping phenotype. We present a unique case and discuss clinical considerations of a patient concurrently exhibiting such conditions with genetic analysis confirming an SCN5A mutation. |
format | Online Article Text |
id | pubmed-5538234 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-55382342017-08-04 Double jeopardy: long QT3 and Brugada syndromes Sandhu, Amneet Borne, Ryan T. Mam, Chandara Bunch, T. Jared Aleong, Ryan G. Clin Case Rep Case Reports Mutations in the SCN5A gene are linked to both the long QT syndrome 3 and Brugada syndrome with few reports describing an overlapping phenotype. We present a unique case and discuss clinical considerations of a patient concurrently exhibiting such conditions with genetic analysis confirming an SCN5A mutation. John Wiley and Sons Inc. 2017-06-30 /pmc/articles/PMC5538234/ /pubmed/28781849 http://dx.doi.org/10.1002/ccr3.1064 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 Sandhu, Amneet Borne, Ryan T. Mam, Chandara Bunch, T. Jared Aleong, Ryan G. Double jeopardy: long QT3 and Brugada syndromes |
title | Double jeopardy: long QT3 and Brugada syndromes |
title_full | Double jeopardy: long QT3 and Brugada syndromes |
title_fullStr | Double jeopardy: long QT3 and Brugada syndromes |
title_full_unstemmed | Double jeopardy: long QT3 and Brugada syndromes |
title_short | Double jeopardy: long QT3 and Brugada syndromes |
title_sort | double jeopardy: long qt3 and brugada syndromes |
topic | Case Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5538234/ https://www.ncbi.nlm.nih.gov/pubmed/28781849 http://dx.doi.org/10.1002/ccr3.1064 |
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