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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2013
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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. |
format | Online Article Text |
id | pubmed-4857274 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
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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