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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...

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Autores principales: Valizadeh, Niloufar, Rafatpanah, Niloofar, Hatami, Farbod, Davari, Mohammad Hossein, Kazemi, Toba
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2021
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.
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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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