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Tricuspid valve dysplasia and Ebstein's anomaly in dogs: case report
(Universidade Federal de Minas Gerais (UFMG), Escola de Veterinária, 2014)
Utilidad de la ecocardiografía en la detección de la insuficiencia cardiaca en un adulto joven con síndrome de origen anómalo de la arteria coronaria izquierda del tronco de la arteria pulmonar y válvula mitral asimétrica similar al paracaídas
(2018)
Objective: To describe a case of a young adult with heart failure, secondary to two rare cardiac malformations, anomalous left coronary artery from the pulmonary artery (ALCAPA) syndrome and parachute-like asymmetric mitral ...
Change in Prevalence of Congenital Defects in Children With Prader-Willi Syndrome
(American Academy of Pediatrics, 2013-02)
OBJECTIVE: The aim of this study was to assess the prevalence of congenital defects observed in patients with Prader-Willi syndrome (PWS) and to compare this prevalence with that described in the general population. In ...
Sonocubic fine: new three-dimensional ultrasound software to the screening of congenital heart diseases
(Sociedade Brasileira de Cirurgia Cardiovascular, 2014-09-01)
Congenital heart disease is the most common fetal congenital malformations; however, the prenatal rate detection still is low. The two-dimensional echocardiography is the gold standard exam to screening and diagnosis of ...
Occlusion of the perimembranous ventricular septal defect using CERA (R) devices
(Wiley-Blackwell, 2012-08-01)
Background High incidence of atrioventricular (AV) block has been the major limitation of percutaneous closure of perimembranous ventricular septal defect (PMVSD). Methods Prospective, multicenter, nonrandomized study ...
The influence of early childhood caries on congenital heart disease: case reportEarly Childhood Caries and Cardiopathy
(Universidade Federal de UberlândiaBrasilOdontologia, 2017)
The Latin American network for congenital malformation surveillance: ReLAMC
(Wiley-liss, div John Wiley & Sons Inc., 2020-12)
The early detection of congenital anomaly epidemics occurs when comparing current with previous frequencies in the same population. The success of epidemiologic surveillance depends on numerous factors, including the ...
Association between phenotype and deletion size in 22q11.2 microdeletion syndrome: systematic review and meta-analysis
(2019)
Background: Chromosome 22q11.2 microdeletion syndrome, a disorder caused by heterozygous loss of genetic material in chromosome region 22q11.2, has a broad range of clinical symptoms. The most common congenital anomalies ...