Literature DB >> 10498154

Clinical outcome in the Marfan syndrome with ascending aortic dilatation followed annually by echocardiography.

M Kornbluth1, I Schnittger, I Eyngorina, C Gasner, D H Liang.   

Abstract

This study reviewed the utility of echocardiography in following patients with the Marfan syndrome for whom cardiovascular complications, especially aortic root dilatation, dissection and rupture, are the major causes of morbidity and mortality. We conclude that echocardiography can be used to follow asymptomatic patients with the Marfan syndrome.

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Year:  1999        PMID： 10498154     DOI： 10.1016/s0002-9149(99)00430-0

Source DB:  PubMed          Journal:  Am J Cardiol        ISSN： 0002-9149            Impact factor:   2.778


  3 in total

1.  Canadian Cardiovascular Society 2009 Consensus Conference on the management of adults with congenital heart disease: outflow tract obstruction, coarctation of the aorta, tetralogy of Fallot, Ebstein anomaly and Marfan's syndrome.

Authors:  Candice K Silversides; Marla Kiess; Luc Beauchesne; Timothy Bradley; Michael Connelly; Koichiro Niwa; Barbara Mulder; Gary Webb; Jack Colman; Judith Therrien
Journal:  Can J Cardiol       Date:  2010-03       Impact factor: 5.223

2.  Does altered aortic flow in marfan syndrome relate to aortic root dilatation?

Authors:  Hung-Hsuan Wang; Hsin-Hui Chiu; Wen-Yih Isaac Tseng; Hsu-Hsia Peng
Journal:  J Magn Reson Imaging       Date:  2016-02-08       Impact factor: 4.813

3.  Magnetic resonance angiography derived predictors of progressive dilatation and surgery of the aortic root in Marfan syndrome.

Authors:  Julius Matthias Weinrich; Alexander Lenz; Gerhard Schön; Cyrus Behzadi; Isabel Molwitz; Frank Oliver Henes; Bjoern Philip Schoennagel; Gerhard Adam; Yskert von Kodolitsch; Peter Bannas
Journal:  PLoS One       Date:  2022-02-03       Impact factor: 3.240
  3 in total

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