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Extended recovery of cardiac function after severe infantile cardiomyopathy presentation of Barth syndrome
Cardiomyopathy is the most common presenting feature of Barth syndrome, often presenting in infancy with severe heart failure and cardiac dysfunction. Historically, affected infants commonly died early after presentation, sometimes before a diagnosis of Barth syndrome was made. With increases in awa...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Inc.
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8898717/ https://www.ncbi.nlm.nih.gov/pubmed/35281665 http://dx.doi.org/10.1002/jmd2.12264 |
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author | Yester, Jessie Feingold, Brian |
author_facet | Yester, Jessie Feingold, Brian |
author_sort | Yester, Jessie |
collection | PubMed |
description | Cardiomyopathy is the most common presenting feature of Barth syndrome, often presenting in infancy with severe heart failure and cardiac dysfunction. Historically, affected infants commonly died early after presentation, sometimes before a diagnosis of Barth syndrome was made. With increases in awareness of Barth syndrome and in the care of infants with severe heart failure, survival of children with Barth syndrome and severe heart failure has improved. We describe our experience caring for five unrelated boys with Barth syndrome who presented with severe cardiomyopathy and heart failure prior to age 2 who have had marked improvement with long‐term response to medical heart failure therapy. |
format | Online Article Text |
id | pubmed-8898717 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley & Sons, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-88987172022-03-11 Extended recovery of cardiac function after severe infantile cardiomyopathy presentation of Barth syndrome Yester, Jessie Feingold, Brian JIMD Rep Case Reports Cardiomyopathy is the most common presenting feature of Barth syndrome, often presenting in infancy with severe heart failure and cardiac dysfunction. Historically, affected infants commonly died early after presentation, sometimes before a diagnosis of Barth syndrome was made. With increases in awareness of Barth syndrome and in the care of infants with severe heart failure, survival of children with Barth syndrome and severe heart failure has improved. We describe our experience caring for five unrelated boys with Barth syndrome who presented with severe cardiomyopathy and heart failure prior to age 2 who have had marked improvement with long‐term response to medical heart failure therapy. John Wiley & Sons, Inc. 2021-12-28 /pmc/articles/PMC8898717/ /pubmed/35281665 http://dx.doi.org/10.1002/jmd2.12264 Text en © 2021 The Authors. JIMD Reports published by John Wiley & Sons Ltd on behalf of SSIEM. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://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 Yester, Jessie Feingold, Brian Extended recovery of cardiac function after severe infantile cardiomyopathy presentation of Barth syndrome |
title | Extended recovery of cardiac function after severe infantile cardiomyopathy presentation of Barth syndrome |
title_full | Extended recovery of cardiac function after severe infantile cardiomyopathy presentation of Barth syndrome |
title_fullStr | Extended recovery of cardiac function after severe infantile cardiomyopathy presentation of Barth syndrome |
title_full_unstemmed | Extended recovery of cardiac function after severe infantile cardiomyopathy presentation of Barth syndrome |
title_short | Extended recovery of cardiac function after severe infantile cardiomyopathy presentation of Barth syndrome |
title_sort | extended recovery of cardiac function after severe infantile cardiomyopathy presentation of barth syndrome |
topic | Case Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8898717/ https://www.ncbi.nlm.nih.gov/pubmed/35281665 http://dx.doi.org/10.1002/jmd2.12264 |
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