Literature DB >> 10147800

Color flow and conventional echocardiography of the Marfan syndrome.

H R Aldrich1, R L Labarre, M J Roman, S E Rosen, M C Spitzer, R B Devereux.   

Abstract

Imaging and color flow Doppler echocardiography are an integral part of any evaluation of a patient with the Marfan syndrome. The major cardiovascular manifestations of this condition are aortic dilation, which may involve the proximal and distal aorta, aortic regurgitation, aortic dissection, mitral valve prolapse, and mitral regurgitation. Patients who have the Marfan syndrome should have serial echocardiograms to measure aortic root diameter carefully at the sinuses of Valsalva and subsequent levels (sinotubular junction, arch, descending and abdominal aorta). Additionally, color Doppler echocardiography assists in the diagnosis of aortic dissection and facilitates evaluation of the severity of aortic and mitral regurgitation that commonly complicate the Marfan syndrome. The risk of aortic dissection, which is the most serious manifestation of the Marfan syndrome, increases as the aorta enlarges. Therefore, elective composite graft surgery is recommended when the aortic root size reaches 60 mm, regardless of symptom status, or 55 mm in the presence of severe aortic regurgitation. Surgical replacement of the aortic root with a composite graft does not end the disease process. Color flow Doppler is useful in the diagnosis of dehiscence of the conduit sewing ring, coronary artery aneurysm, distal aortic dissections, and prosthetic valve dysfunction.

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Year:  1992        PMID: 10147800     DOI: 10.1111/j.1540-8175.1992.tb00508.x

Source DB:  PubMed          Journal:  Echocardiography        ISSN: 0742-2822            Impact factor:   1.724


  3 in total

1.  Aortic root asymmetry in marfan patients; evaluation by magnetic resonance imaging and comparison with standard echocardiography.

Authors:  L J Meijboom; M Groenink; E E van der Wall; H Romkes; J Stoker; B J Mulder
Journal:  Int J Card Imaging       Date:  2000-06

2.  The economic impact of Marfan syndrome: a non-experimental, retrospective, population-based matched cohort study.

Authors:  Dmitrij Achelrod; Carl Rudolf Blankart; Roland Linder; Yskert von Kodolitsch; Tom Stargardt
Journal:  Orphanet J Rare Dis       Date:  2014-06-23       Impact factor: 4.123

Review 3.  Marfan syndrome: current perspectives.

Authors:  Guglielmina Pepe; Betti Giusti; Elena Sticchi; Rosanna Abbate; Gian Franco Gensini; Stefano Nistri
Journal:  Appl Clin Genet       Date:  2016-05-09
  3 in total

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