Huge isolate abdominal aorta aneurysm in a 24-year-old patient with Marfan syndrome in CT imaging in view of recent literature

Journal Title: Journal of Pre-Clinical and Clinical Research - Year 2008, Vol 2, Issue 1

Abstract

The Marfan 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 young patient with a progressive advanced abdominal aorta dilatation visualized on CT images is presented. Pathogenesis, diagnosis and management of patients with Marfan syndrome are also discussed.

Authors and Affiliations

Ewa Kurys-Denis, Witold Krupski

Keywords

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  • EP ID EP58602
  • DOI -
  • Views 104
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How To Cite

Ewa Kurys-Denis, Witold Krupski (2008). Huge isolate abdominal aorta aneurysm in a 24-year-old patient with Marfan syndrome in CT imaging in view of recent literature. Journal of Pre-Clinical and Clinical Research, 2(1), 85-87. https://www.europub.co.uk/articles/-A-58602