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Isolated infrarenal abdominal aorta aneurysm in a 42-year-old patient with Marfan’s syndrome: Case report

Marfan’s syndrome is an autosomal dominant disorder of connective tissue characterized by a large number of possible mutations and by heterogeneity of clinical presentation primarily in skeletal, ocular and cardiovascular organ systems. Cardiovascular complications of the disease are responsible for...

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Autores principales: Jiber, Hamid, Hajji, Rita, Zrihni, Youssef, Zaghloul, Rachid, Zizi, Othman, Bouarhroum, Abdellatif
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4857274/
https://www.ncbi.nlm.nih.gov/pubmed/27489631
http://dx.doi.org/10.1177/2050313X13507564
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author Jiber, Hamid
Hajji, Rita
Zrihni, Youssef
Zaghloul, Rachid
Zizi, Othman
Bouarhroum, Abdellatif
author_facet Jiber, Hamid
Hajji, Rita
Zrihni, Youssef
Zaghloul, Rachid
Zizi, Othman
Bouarhroum, Abdellatif
author_sort Jiber, Hamid
collection PubMed
description Marfan’s syndrome is an autosomal dominant disorder of connective tissue characterized by a large number of possible mutations and by heterogeneity of clinical presentation primarily in skeletal, ocular and cardiovascular organ systems. Cardiovascular complications of the disease are responsible for high mortality. The case of a 42-year-old patient with a progressive advanced abdominal aorta dilatation visualized on computed tomography images is presented. Pathogenesis, diagnosis and management of patients with Marfan’s syndrome are also discussed.
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spelling pubmed-48572742016-08-03 Isolated infrarenal abdominal aorta aneurysm in a 42-year-old patient with Marfan’s syndrome: Case report Jiber, Hamid Hajji, Rita Zrihni, Youssef Zaghloul, Rachid Zizi, Othman Bouarhroum, Abdellatif SAGE Open Med Case Rep Case Report Marfan’s syndrome is an autosomal dominant disorder of connective tissue characterized by a large number of possible mutations and by heterogeneity of clinical presentation primarily in skeletal, ocular and cardiovascular organ systems. Cardiovascular complications of the disease are responsible for high mortality. The case of a 42-year-old patient with a progressive advanced abdominal aorta dilatation visualized on computed tomography images is presented. Pathogenesis, diagnosis and management of patients with Marfan’s syndrome are also discussed. SAGE Publications 2013-10-01 /pmc/articles/PMC4857274/ /pubmed/27489631 http://dx.doi.org/10.1177/2050313X13507564 Text en © The Author(s) 2013 http://creativecommons.org/licenses/by-nc/3.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 3.0 License (http://www.creativecommons.org/licenses/by-nc/3.0/) 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(http://www.uk.sagepub.com/aboutus/openaccess.htm).
spellingShingle Case Report
Jiber, Hamid
Hajji, Rita
Zrihni, Youssef
Zaghloul, Rachid
Zizi, Othman
Bouarhroum, Abdellatif
Isolated infrarenal abdominal aorta aneurysm in a 42-year-old patient with Marfan’s syndrome: Case report
title Isolated infrarenal abdominal aorta aneurysm in a 42-year-old patient with Marfan’s syndrome: Case report
title_full Isolated infrarenal abdominal aorta aneurysm in a 42-year-old patient with Marfan’s syndrome: Case report
title_fullStr Isolated infrarenal abdominal aorta aneurysm in a 42-year-old patient with Marfan’s syndrome: Case report
title_full_unstemmed Isolated infrarenal abdominal aorta aneurysm in a 42-year-old patient with Marfan’s syndrome: Case report
title_short Isolated infrarenal abdominal aorta aneurysm in a 42-year-old patient with Marfan’s syndrome: Case report
title_sort isolated infrarenal abdominal aorta aneurysm in a 42-year-old patient with marfan’s syndrome: case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4857274/
https://www.ncbi.nlm.nih.gov/pubmed/27489631
http://dx.doi.org/10.1177/2050313X13507564
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