Quadricuspid Aortic Valve: Three Cases Report and Literature Review

AUTOR(ES)

Veronese, Elinthon Tavares

FONTE

Braz. J. Cardiovasc. Surg.

DATA DE PUBLICAÇÃO

11/11/2019

RESUMO

Abstract Quadricuspid aortic valve (QAV) is a rare cardiac malformation. Many cases are incidentally diagnosed in aortic surgeries or autopsies and it usually appears as an isolated anomaly. The most widely classification used is the one by Hurwitz and Roberts[1], which divides 7 alphabetical subtypes based on the cusps size. The aim of this report is to describe three different anatomic presentations of this rare aortic valve anomaly.

Documentos Relacionados

• Quadricuspid Aortic Valve: Case Report and Review of the Literature
• Quadricuspid Aortic Valve: A Comprehensive Review
• Congenital quadricuspid aortic valve anomaly associated with hypertrophic non-obstructive cardiomyopathy: a case report and review of the literature.
• Chronic thrombosed abdominal aortic aneurysms: a report on three consecutive cases and literature review
• Quadricuspid Aortic Valve