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Literature DB >> 17019535

Surgical correction of mitral valve prolapse : a cure for recurrent ventricular tachycardia in Marfan syndrome?

Rebecca S Beroukhim¹, John H Reed, Michael S Schaffer, Anji T Yetman.

Abstract

We describe the case of a 3-year-old child with neonatal Marfan syndrome complicated by mitral valve prolapse with regurgitation, marked aortic root dilatation, and ventricular tachycardia. The patient had resolution of ventricular tachycardia following surgical intervention consisting of a valve-sparing aortic root replacement and mitral valve annuloplasty.

Entities: Disease Species

Mesh：

Substances：

Year: 2006 PMID： 17019535 DOI： 10.1007/s00246-006-1102-0

Source DB: PubMed Journal: Pediatr Cardiol ISSN： 0172-0643 Impact factor: 1.655

8 in total

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Journal: Am Heart J Date: 1977-06 Impact factor: 4.749

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3. Long-term outcome in patients with Marfan syndrome: is aortic dissection the only cause of sudden death?

Authors: Anji T Yetman; Renee A Bornemeier; Brian W McCrindle
Journal: J Am Coll Cardiol Date: 2003-01-15 Impact factor: 24.094

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Journal: Circulation Date: 1983-03 Impact factor: 29.690

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Authors: R E Kavey; M S Blackman; H M Sondheimer; C J Byrum
Journal: J Pediatr Date: 1984-12 Impact factor: 4.406

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Journal: Am J Med Date: 1977-03 Impact factor: 4.965

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8 in total

4 in total

Surgical correction of mitral valve prolapse : a cure for recurrent ventricular tachycardia in Marfan syndrome?

1. Ventricular buckling: a factor in the abnormal ventriculogram and peculiar hemodynamics associated with mitral valve prolapse.

2. Revised diagnostic criteria for the Marfan syndrome.

3. Long-term outcome in patients with Marfan syndrome: is aortic dissection the only cause of sudden death?

4. Ventricular dysrhythmias in children with Marfan's syndrome.

5. The myxomatous mitral valve and sudden death.

6. Ventricular arrhythmias and mitral valve prolapse in childhood.

7. Mitral valve prolapse: a review of associated arrhythmias.

8. Refractory ventricular arrhythmias in a patient with mitral valve prolapse. Successful control with mitral valve replacement.

1. Atrial ectopic tachycardia in a patient with marfan syndrome.

2. Total chordal augmentation in a child with Marfan syndrome and severe mitral insufficiency.

3. Unprovoked Pulmonary Embolism in a Young Patient with Marfan Syndrome.

4. Spontaneous Right Ventricular Pseudoaneurysms and Increased Arrhythmogenicity in a Mouse Model of Marfan Syndrome.