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Desmoplakin cardiomyopathy—an inherited cardiomyopathy presenting with recurrent episodes of acute myocardial injury
We present two female patients with recurrent episodes of myocardial injury, consisting of acute chest pain and elevated cardiac markers without coronary artery disease. Cardiovascular magnetic resonance imaging identified extensive late gadolinium enhancement suggestive of an inherited cardiomyopat...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Bohn Stafleu van Loghum
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10400739/ https://www.ncbi.nlm.nih.gov/pubmed/36434384 http://dx.doi.org/10.1007/s12471-022-01735-2 |
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author | Schoonvelde, S. A. C. Hirsch, A. Yap, S. C. Verhagen, J. M. A. van Slegtenhorst, M. A. Segers, D. van Loon, J. E. Michels, M. |
author_facet | Schoonvelde, S. A. C. Hirsch, A. Yap, S. C. Verhagen, J. M. A. van Slegtenhorst, M. A. Segers, D. van Loon, J. E. Michels, M. |
author_sort | Schoonvelde, S. A. C. |
collection | PubMed |
description | We present two female patients with recurrent episodes of myocardial injury, consisting of acute chest pain and elevated cardiac markers without coronary artery disease. Cardiovascular magnetic resonance imaging identified extensive late gadolinium enhancement suggestive of an inherited cardiomyopathy. Genetic testing showed heterozygous pathogenic variants in the desmoplakin (DSP) gene, the gene coding for the desmoplakin protein, a structural protein found in the cardiac desmosome. Pathogenic variants in the DSP gene are associated with dilated and arrhythmogenic cardiomyopathy. DSP cardiomyopathies may cause recurring myocardial injury mimicking an acute coronary syndrome or myocarditis. Cardiac magnetic resonance imaging is key in its diagnosis due to its specifying imaging features. Genetic testing is essential for the evaluation and confirmation of the diagnosis. VIDEO ONLINE: The online version of this article contains 2 videos. The article and the videos are online available (10.1007/s12471-022-01735-2). The videos can be found in the article back matter as “Electronic Supplementary Material”. |
format | Online Article Text |
id | pubmed-10400739 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Bohn Stafleu van Loghum |
record_format | MEDLINE/PubMed |
spelling | pubmed-104007392023-08-05 Desmoplakin cardiomyopathy—an inherited cardiomyopathy presenting with recurrent episodes of acute myocardial injury Schoonvelde, S. A. C. Hirsch, A. Yap, S. C. Verhagen, J. M. A. van Slegtenhorst, M. A. Segers, D. van Loon, J. E. Michels, M. Neth Heart J Point of View We present two female patients with recurrent episodes of myocardial injury, consisting of acute chest pain and elevated cardiac markers without coronary artery disease. Cardiovascular magnetic resonance imaging identified extensive late gadolinium enhancement suggestive of an inherited cardiomyopathy. Genetic testing showed heterozygous pathogenic variants in the desmoplakin (DSP) gene, the gene coding for the desmoplakin protein, a structural protein found in the cardiac desmosome. Pathogenic variants in the DSP gene are associated with dilated and arrhythmogenic cardiomyopathy. DSP cardiomyopathies may cause recurring myocardial injury mimicking an acute coronary syndrome or myocarditis. Cardiac magnetic resonance imaging is key in its diagnosis due to its specifying imaging features. Genetic testing is essential for the evaluation and confirmation of the diagnosis. VIDEO ONLINE: The online version of this article contains 2 videos. The article and the videos are online available (10.1007/s12471-022-01735-2). The videos can be found in the article back matter as “Electronic Supplementary Material”. Bohn Stafleu van Loghum 2022-11-26 2023-08 /pmc/articles/PMC10400739/ /pubmed/36434384 http://dx.doi.org/10.1007/s12471-022-01735-2 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Point of View Schoonvelde, S. A. C. Hirsch, A. Yap, S. C. Verhagen, J. M. A. van Slegtenhorst, M. A. Segers, D. van Loon, J. E. Michels, M. Desmoplakin cardiomyopathy—an inherited cardiomyopathy presenting with recurrent episodes of acute myocardial injury |
title | Desmoplakin cardiomyopathy—an inherited cardiomyopathy presenting with recurrent episodes of acute myocardial injury |
title_full | Desmoplakin cardiomyopathy—an inherited cardiomyopathy presenting with recurrent episodes of acute myocardial injury |
title_fullStr | Desmoplakin cardiomyopathy—an inherited cardiomyopathy presenting with recurrent episodes of acute myocardial injury |
title_full_unstemmed | Desmoplakin cardiomyopathy—an inherited cardiomyopathy presenting with recurrent episodes of acute myocardial injury |
title_short | Desmoplakin cardiomyopathy—an inherited cardiomyopathy presenting with recurrent episodes of acute myocardial injury |
title_sort | desmoplakin cardiomyopathy—an inherited cardiomyopathy presenting with recurrent episodes of acute myocardial injury |
topic | Point of View |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10400739/ https://www.ncbi.nlm.nih.gov/pubmed/36434384 http://dx.doi.org/10.1007/s12471-022-01735-2 |
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