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Genetically Triggered Thoracic Aortic Disease: Who Should be Tested?
Up to 25% of patients with thoracic aortic disease have an underlying Mendelian pathogenic variant. This is a heterogeneous group of disorders known as heritable thoracic aortic diseases (HTAD). Diagnosing associated pathogenic gene variants and syndromes is critical, as the underlying genetics have...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Houston Methodist DeBakey Heart & Vascular Center
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10000331/ https://www.ncbi.nlm.nih.gov/pubmed/36910552 http://dx.doi.org/10.14797/mdcvj.1218 |
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author | Duarte, Valeria E. Yousefzai, Raman Singh, Michael N. |
author_facet | Duarte, Valeria E. Yousefzai, Raman Singh, Michael N. |
author_sort | Duarte, Valeria E. |
collection | PubMed |
description | Up to 25% of patients with thoracic aortic disease have an underlying Mendelian pathogenic variant. This is a heterogeneous group of disorders known as heritable thoracic aortic diseases (HTAD). Diagnosing associated pathogenic gene variants and syndromes is critical, as the underlying genetics have an implication in medical management, surveillance, thresholds for surgical intervention, surgical risk, pregnancy risk, and risk of inheritance by the offspring. Recently released 2022 American College of Cardiology/American Heart Association guidelines for the diagnosis and management of aortic diseases provide specific recommendations to identify patients at risk for heritable conditions and who should undergo genetic testing. |
format | Online Article Text |
id | pubmed-10000331 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Houston Methodist DeBakey Heart & Vascular Center |
record_format | MEDLINE/PubMed |
spelling | pubmed-100003312023-03-11 Genetically Triggered Thoracic Aortic Disease: Who Should be Tested? Duarte, Valeria E. Yousefzai, Raman Singh, Michael N. Methodist Debakey Cardiovasc J Review Up to 25% of patients with thoracic aortic disease have an underlying Mendelian pathogenic variant. This is a heterogeneous group of disorders known as heritable thoracic aortic diseases (HTAD). Diagnosing associated pathogenic gene variants and syndromes is critical, as the underlying genetics have an implication in medical management, surveillance, thresholds for surgical intervention, surgical risk, pregnancy risk, and risk of inheritance by the offspring. Recently released 2022 American College of Cardiology/American Heart Association guidelines for the diagnosis and management of aortic diseases provide specific recommendations to identify patients at risk for heritable conditions and who should undergo genetic testing. Houston Methodist DeBakey Heart & Vascular Center 2023-03-07 /pmc/articles/PMC10000331/ /pubmed/36910552 http://dx.doi.org/10.14797/mdcvj.1218 Text en Copyright: © 2023 The Author(s) https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International License (CC-BY 4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. See http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Review Duarte, Valeria E. Yousefzai, Raman Singh, Michael N. Genetically Triggered Thoracic Aortic Disease: Who Should be Tested? |
title | Genetically Triggered Thoracic Aortic Disease: Who Should be Tested? |
title_full | Genetically Triggered Thoracic Aortic Disease: Who Should be Tested? |
title_fullStr | Genetically Triggered Thoracic Aortic Disease: Who Should be Tested? |
title_full_unstemmed | Genetically Triggered Thoracic Aortic Disease: Who Should be Tested? |
title_short | Genetically Triggered Thoracic Aortic Disease: Who Should be Tested? |
title_sort | genetically triggered thoracic aortic disease: who should be tested? |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10000331/ https://www.ncbi.nlm.nih.gov/pubmed/36910552 http://dx.doi.org/10.14797/mdcvj.1218 |
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