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Twenty Years’ Follow-up of a Family with Marfan Syndrome: A Case Series
Marfan syndrome is a rare connective tissue disorder manifesting with cardiovascular pathologies which are also the leading cause of death. Herein, we present the past 20 years follow up of a family with 17 members afflicted with Marfan syndrome. 3 members of the family were deceased and none were d...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer - Medknow
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8445147/ https://www.ncbi.nlm.nih.gov/pubmed/34584630 http://dx.doi.org/10.4103/HEARTVIEWS.HEARTVIEWS_88_20 |
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author | Valizadeh, Niloufar Rafatpanah, Niloofar Hatami, Farbod Davari, Mohammad Hossein Kazemi, Toba |
author_facet | Valizadeh, Niloufar Rafatpanah, Niloofar Hatami, Farbod Davari, Mohammad Hossein Kazemi, Toba |
author_sort | Valizadeh, Niloufar |
collection | PubMed |
description | Marfan syndrome is a rare connective tissue disorder manifesting with cardiovascular pathologies which are also the leading cause of death. Herein, we present the past 20 years follow up of a family with 17 members afflicted with Marfan syndrome. 3 members of the family were deceased and none were due to cardiovascular events. We assume to some extent traumas are a neglected cause for a part of mortality in Marfan syndrome. |
format | Online Article Text |
id | pubmed-8445147 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Wolters Kluwer - Medknow |
record_format | MEDLINE/PubMed |
spelling | pubmed-84451472021-09-27 Twenty Years’ Follow-up of a Family with Marfan Syndrome: A Case Series Valizadeh, Niloufar Rafatpanah, Niloofar Hatami, Farbod Davari, Mohammad Hossein Kazemi, Toba Heart Views Case Report Marfan syndrome is a rare connective tissue disorder manifesting with cardiovascular pathologies which are also the leading cause of death. Herein, we present the past 20 years follow up of a family with 17 members afflicted with Marfan syndrome. 3 members of the family were deceased and none were due to cardiovascular events. We assume to some extent traumas are a neglected cause for a part of mortality in Marfan syndrome. Wolters Kluwer - Medknow 2021 2021-08-19 /pmc/articles/PMC8445147/ /pubmed/34584630 http://dx.doi.org/10.4103/HEARTVIEWS.HEARTVIEWS_88_20 Text en Copyright: © 2021 Heart Views https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms. |
spellingShingle | Case Report Valizadeh, Niloufar Rafatpanah, Niloofar Hatami, Farbod Davari, Mohammad Hossein Kazemi, Toba Twenty Years’ Follow-up of a Family with Marfan Syndrome: A Case Series |
title | Twenty Years’ Follow-up of a Family with Marfan Syndrome: A Case Series |
title_full | Twenty Years’ Follow-up of a Family with Marfan Syndrome: A Case Series |
title_fullStr | Twenty Years’ Follow-up of a Family with Marfan Syndrome: A Case Series |
title_full_unstemmed | Twenty Years’ Follow-up of a Family with Marfan Syndrome: A Case Series |
title_short | Twenty Years’ Follow-up of a Family with Marfan Syndrome: A Case Series |
title_sort | twenty years’ follow-up of a family with marfan syndrome: a case series |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8445147/ https://www.ncbi.nlm.nih.gov/pubmed/34584630 http://dx.doi.org/10.4103/HEARTVIEWS.HEARTVIEWS_88_20 |
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