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Marfan Syndrome - Acute Aortic Dissection Due to Giant Aortic Aneurysm

Marfan syndrome is a genetic disorder with an estimated prevalence of 1/5000 births. Clinical manifestation and disease progress can vary among individuals affected therefore serial follow-up examinations are mandatory in order to prevent serious complications.We report a case of giant proximal aort...

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Autores principales: MUNTEANU, O., DONOIU, I., ISTRATOAIE, O., MILITARU, C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medical University Publishing House Craiova 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6286717/
https://www.ncbi.nlm.nih.gov/pubmed/30595862
http://dx.doi.org/10.12865/CHSJ.43.01.15
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author MUNTEANU, O.
DONOIU, I.
ISTRATOAIE, O.
MILITARU, C.
author_facet MUNTEANU, O.
DONOIU, I.
ISTRATOAIE, O.
MILITARU, C.
author_sort MUNTEANU, O.
collection PubMed
description Marfan syndrome is a genetic disorder with an estimated prevalence of 1/5000 births. Clinical manifestation and disease progress can vary among individuals affected therefore serial follow-up examinations are mandatory in order to prevent serious complications.We report a case of giant proximal aorta aneurysm with associated aortic dissection in a young patient with Marfan syndrome who neglected medical advice to undergo periodic medical evaluation.Given the fact that clinical manifestations may differ among patients making prediction of disease progression very difficult, the patient with Marfan syndrome should be carefully monitored.
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spelling pubmed-62867172018-12-28 Marfan Syndrome - Acute Aortic Dissection Due to Giant Aortic Aneurysm MUNTEANU, O. DONOIU, I. ISTRATOAIE, O. MILITARU, C. Curr Health Sci J Case Report Marfan syndrome is a genetic disorder with an estimated prevalence of 1/5000 births. Clinical manifestation and disease progress can vary among individuals affected therefore serial follow-up examinations are mandatory in order to prevent serious complications.We report a case of giant proximal aorta aneurysm with associated aortic dissection in a young patient with Marfan syndrome who neglected medical advice to undergo periodic medical evaluation.Given the fact that clinical manifestations may differ among patients making prediction of disease progression very difficult, the patient with Marfan syndrome should be carefully monitored. Medical University Publishing House Craiova 2017 2017-09-27 /pmc/articles/PMC6286717/ /pubmed/30595862 http://dx.doi.org/10.12865/CHSJ.43.01.15 Text en Copyright © 2017, Medical University Publishing House Craiova http://creativecommons.org/licenses/by-nc-sa/4.0/ This is an open-access article distributed under the terms of a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Public License, which permits unrestricted use, adaptation, distribution and reproduction in any medium, non-commercially, provided the new creations are licensed under identical terms as the original work and the original work is properly cited.
spellingShingle Case Report
MUNTEANU, O.
DONOIU, I.
ISTRATOAIE, O.
MILITARU, C.
Marfan Syndrome - Acute Aortic Dissection Due to Giant Aortic Aneurysm
title Marfan Syndrome - Acute Aortic Dissection Due to Giant Aortic Aneurysm
title_full Marfan Syndrome - Acute Aortic Dissection Due to Giant Aortic Aneurysm
title_fullStr Marfan Syndrome - Acute Aortic Dissection Due to Giant Aortic Aneurysm
title_full_unstemmed Marfan Syndrome - Acute Aortic Dissection Due to Giant Aortic Aneurysm
title_short Marfan Syndrome - Acute Aortic Dissection Due to Giant Aortic Aneurysm
title_sort marfan syndrome - acute aortic dissection due to giant aortic aneurysm
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6286717/
https://www.ncbi.nlm.nih.gov/pubmed/30595862
http://dx.doi.org/10.12865/CHSJ.43.01.15
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