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Hypertrophic Cardiomyopathy in the Elderly: A Case Identified With Genetic Screening

Hypertrophic cardiomyopathy (HCM) is a hereditary disease with an autosomal dominant pattern of inheritance, that is caused by a mutation in one of several sarcomere genes that encodes components of the contractile system of the heart. Hypertrophic cardiomyopathy has been described as a disease that...

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Autores principales: Del Rio-Pertuz, Gaspar, Sethi, Pooja, Swaminath, Deephak, Argueta-Sosa, Erwin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9251991/
https://www.ncbi.nlm.nih.gov/pubmed/35778879
http://dx.doi.org/10.1177/23247096221109204
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author Del Rio-Pertuz, Gaspar
Sethi, Pooja
Swaminath, Deephak
Argueta-Sosa, Erwin
author_facet Del Rio-Pertuz, Gaspar
Sethi, Pooja
Swaminath, Deephak
Argueta-Sosa, Erwin
author_sort Del Rio-Pertuz, Gaspar
collection PubMed
description Hypertrophic cardiomyopathy (HCM) is a hereditary disease with an autosomal dominant pattern of inheritance, that is caused by a mutation in one of several sarcomere genes that encodes components of the contractile system of the heart. Hypertrophic cardiomyopathy has been described as a disease that is more heavily diagnosed in the second decade of life, that may present with abnormal syncopal episodes or sudden cardiac death. However, with a better understanding of the genetic changes that occur in HCM and with improved imaging techniques, there has now been an increased recognition of a late-onset disease that can occur in the elderly population. We report a case of a 73-year-old woman who was found to have HCM after various clinical events took place.
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spelling pubmed-92519912022-07-05 Hypertrophic Cardiomyopathy in the Elderly: A Case Identified With Genetic Screening Del Rio-Pertuz, Gaspar Sethi, Pooja Swaminath, Deephak Argueta-Sosa, Erwin J Investig Med High Impact Case Rep Case Report Hypertrophic cardiomyopathy (HCM) is a hereditary disease with an autosomal dominant pattern of inheritance, that is caused by a mutation in one of several sarcomere genes that encodes components of the contractile system of the heart. Hypertrophic cardiomyopathy has been described as a disease that is more heavily diagnosed in the second decade of life, that may present with abnormal syncopal episodes or sudden cardiac death. However, with a better understanding of the genetic changes that occur in HCM and with improved imaging techniques, there has now been an increased recognition of a late-onset disease that can occur in the elderly population. We report a case of a 73-year-old woman who was found to have HCM after various clinical events took place. SAGE Publications 2022-07-01 /pmc/articles/PMC9251991/ /pubmed/35778879 http://dx.doi.org/10.1177/23247096221109204 Text en © 2022 American Federation for Medical Research https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Case Report
Del Rio-Pertuz, Gaspar
Sethi, Pooja
Swaminath, Deephak
Argueta-Sosa, Erwin
Hypertrophic Cardiomyopathy in the Elderly: A Case Identified With Genetic Screening
title Hypertrophic Cardiomyopathy in the Elderly: A Case Identified With Genetic Screening
title_full Hypertrophic Cardiomyopathy in the Elderly: A Case Identified With Genetic Screening
title_fullStr Hypertrophic Cardiomyopathy in the Elderly: A Case Identified With Genetic Screening
title_full_unstemmed Hypertrophic Cardiomyopathy in the Elderly: A Case Identified With Genetic Screening
title_short Hypertrophic Cardiomyopathy in the Elderly: A Case Identified With Genetic Screening
title_sort hypertrophic cardiomyopathy in the elderly: a case identified with genetic screening
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9251991/
https://www.ncbi.nlm.nih.gov/pubmed/35778879
http://dx.doi.org/10.1177/23247096221109204
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