Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Mitral Valve Atresia"'
OBJECTIVES To analyze near-term cerebroplacental Doppler, heart morphology, and neonatal biometry in isolated hypoplastic left heart syndrome (HLHS) relative to healthy controls. METHODS This retrospective study included 55 fetuses with HLHS (29 with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::52a50dda1ab70a4639e9b069b35d4fc7
https://ruj.uj.edu.pl/xmlui/handle/item/285619
https://ruj.uj.edu.pl/xmlui/handle/item/285619
Publikováno v:
Cardiology in the young. 31(12)
We describe two cases of an unusual variant of double outlet right ventricle with intact ventricular septum diagnosed prenatally and confirmed by foetal autopsy in a case. The first case had mitral valve atresia, slit-like left ventricle, and normall
Autor:
Brienne McKenzie, Evan W. Matshes
Publikováno v:
Academic Forensic Pathology. 2:374-378
Truncus arteriosus is a rare congenital heart defect characterized by a single common arterial trunk giving rise to both the pulmonary and systemic arteries. Concurrent cardiac abnormalities are common. In the absence of surgical intervention, the co
Publikováno v:
Journal of Clinical Ultrasound. 33:197-200
We present a case of heterotaxy syndrome with right isomerism detected in a twin fetus, with the sonographic findings that established this diagnosis. At 24 weeks' menstrual age, ultrasound detected anomalies in the heart suggestive of heterotaxy syn
Autor:
Andres Menesses, Jeffrey A. Towbin, John W. Belmont, Ana Combes, Mark B. Lewin, Louis I. Bezold, Ricardo H. Pignatelli, Wilbur A. Lam, Norman L. Kaplan, Kim L. McBride, Susan D. Fernbach
Publikováno v:
PEDIATRICS. 114:691-696
Objective. Left ventricular outflow tract obstructive (LVOTO) malformations are a leading cause of infant mortality from birth defects. Genetic mechanisms are likely, and there may be a higher rate of asymptomatic LVOTO anomalies in relatives of affe
Autor:
Beatrice Havarani, Glenn L. Renforth, Helen M. Phillips, Oliver Stumper, Tom Hearn, Cosma Spalluto, Tony Salmon, M Clement-Jones, A Curtis, Lyndsey Craven, Michael S. Jackson, Susie Hutchinson, Carol English, David I. Wilson
Publikováno v:
Genomics. 79:475-478
Hypoplastic left heart is a severe human congenital heart defect characterized by left ventricular hypoplasiawith aortic and mitral valve atresia. A genetic etiology is indicated by an association of the hypoplastic left heart phenotype with terminal
Autor:
N. Sreeram
Publikováno v:
Current Paediatrics. 6:156-161
Hypoplastic left heart syndrome (HLHS) represents a spectrum of lesions having in common hypoplasia of the left ventricle, in association with aortic valve atresia or stenosis, mitral valve atresia or stenosis and hypoplasia of the aortic arch. l The
Publikováno v:
Heart. 71:588-595
OBJECTIVE--To determine the incidence of the various types of obstruction of the left ventricular outflow tract in patients born in the five health districts of Liverpool and to compare their prognosis into early adult life. DESIGN--Notes of all pati
Publikováno v:
Pediatric Cardiology. 20:200-202
Abnormalities of the mitral valve (MV) or the tricuspid valve (TV) morphology and/or function in patients with functional single ventricle may result in early morbidity and death. The purpose of this study was to determine the incidence of contralate
Publikováno v:
The Annals of thoracic surgery. 65(1)
A rare case of truncus arteriosus associated with mitral valve atresia, hypoplastic left ventricle, and intact ventricular septum is reported. Successful medical management and surgical palliation of this defect is described. The possible embryology,