Literature DB >> 3348700

Marfan's syndrome: combined composite valve graft replacement of the aortic root and transaortic mitral valve replacement.

E S Crawford1, J S Coselli.   

Abstract

Echocardiographic studies in patients with Marfan's syndrome indicate that 95% eventually have aortic root dilatation, mitral valve prolapse, or a combination of these. Both lesions can progress and require operation for aortic root aneurysm, aortic valve insufficiency, and mitral valve insufficiency. This report reviews the simplified treatment of 6 patients by combined composite valve graft replacement of the aortic root and transaortic mitral valve replacement at one operation. All patients survived and are well for periods extending from 1 month to 12 months.

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Year:  1988        PMID: 3348700     DOI: 10.1016/s0003-4975(10)62466-6

Source DB:  PubMed          Journal:  Ann Thorac Surg        ISSN: 0003-4975            Impact factor:   4.330


  2 in total

1.  [Surgical treatment of cardiovascular manifestations of Marfan's syndrome].

Authors:  R Lange; E Ebert
Journal:  Herz       Date:  1999-12       Impact factor: 1.443

2.  Transaortic double valve replacement with total chordal preservation.

Authors:  Smartin Abraham; Raja Joshi; A Sampath Kumar
Journal:  Tex Heart Inst J       Date:  2002
  2 in total

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