Correção cirúrgica da estenose aórtica supravalvar com modificação da técnica de Sousa

Bonini, Rômulo César Arnal; Palazzi, Eugenio Molina; Chaccur, Paulo; Sousa, Luiz

doi:10.1590/s0102-76382010000200021

Cited by 3 publications

(2 citation statements)

References 6 publications

(9 reference statements)

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“…The supravalvular aortic stenosis (SAS) is the least common form of obstruction of the left ventricular outflow tract, representing 0.05% of all congenital heart disease [ 1 - 3 ] . It is characterized as a congenital obstruction of the ascending aorta, most commonly involving the sinotubular junction and may occur as a dysmorphia like an "hourglass" or as a diffuse hyperplasia.…”

Section: Introductionmentioning

confidence: 99%

Supravalvular aortic stenosis in adult with anomalies of aortic arch vessels and aortic regurgitation

Valente

Alencar

et al. 2013

Revista Brasileira De Cirurgia Cardiovascular

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Section: Introductionmentioning

confidence: 99%

Supravalvular aortic stenosis in adult with anomalies of aortic arch vessels and aortic regurgitation

Valente

Alencar

et al. 2013

Revista Brasileira De Cirurgia Cardiovascular

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“…The degenerative calcification of the aortic valve is considered the most common cause of aortic stenosis in developed countries, the most frequent indication for aortic valve replacement [1][2][3][4][5]. Standard treatment involves replacing of the valve by a prosthetic device (biological or mechanical) with operative mortality around 4% [6.7].…”

Section: Introductionmentioning

confidence: 99%

Implante transcateter de valva aórtica

Gaia¹,

Palma²,

Ferreira³

et al. 2011

Rev Bras Cir Cardiovasc

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Congenital heart defects in Williams syndrome

Yuan¹

2017

Turk J Pediatr

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Williams syndrome (WS), also known as Williams-Beuren syndrome, is a rare genetic disorder involving multiple systems including the circulatory system. However, the etiologies of the associated congenital heart defects in WS patients have not been sufficiently elucidated and represent therapeutic challenges. The typical congenital heart defects in WS were supravalvar aortic stenosis, pulmonary stenosis (both valvular and peripheral), aortic coarctation and mitral valvar prolapse. The atypical cardiovascular anomalies include tetralogy of Fallot, atrial septal defects, aortic and mitral valvular insufficiencies, bicuspid aortic valves, ventricular septal defects, total anomalous pulmonary venous return, double chambered right ventricle, Ebstein anomaly and arterial anomalies. Deletion of the elastin gene on chromosome 7q11.23 leads to deficiency or abnormal deposition of elastin during cardiovascular development, thereby leading to widespread cardiovascular abnormalities in WS. In this article, the distribution, treatment and surgical outcomes of typical and atypical cardiac defects in WS are discussed.

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Correção cirúrgica da estenose aórtica supravalvar com modificação da técnica de Sousa

Cited by 3 publications

References 6 publications

Supravalvular aortic stenosis in adult with anomalies of aortic arch vessels and aortic regurgitation

Supravalvular aortic stenosis in adult with anomalies of aortic arch vessels and aortic regurgitation

Implante transcateter de valva aórtica

Congenital heart defects in Williams syndrome

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