نتایج جستجو برای: atrial septal defect asd
تعداد نتایج: 199251 فیلتر نتایج به سال:
BACKGROUND Congenital heart disease (CHD) is frequently described in patients with Down syndrome (DS) and is the main cause of death in this population during the first two years of life. The spectrum of CHD patterns in DS varies widely worldwide; this variation could be due to sociodemographic, genetic and geographic factors. METHODS A six-year retrospective, descriptive study was carried ou...
Background: Several epidemiologic studies indicate that some paternal occupations are associated with an increased risk of birth defects in offspring. Possible associations between paternal exposures and cardiovascular malformations were evaluated in previous studies. Material and methods: The case-control study was performed during an academic year between October 1999 and 2000. All children ...
OBJECTIVES This study sought to compare the safety and efficacy of the HELEX septal occluder (HSO) with surgical repair of atrial septal defect (ASD). BACKGROUND The HSO is a low-profile, double-disk occluder device for percutaneous closure of secundum ASD. METHODS Patients were enrolled (HSO arm prospectively, surgery arm prospectively/retrospectively) from 14 U.S. sites and followed up fo...
Forty percent of people with Down syndrome exhibit heart defects, most often an atrioventricular septal defect (AVSD) and less frequently a ventricular septal defect (VSD) or atrial septal defect (ASD). Lymphoblastoid cell lines (LCLs) were established from lymphocytes of individuals with trisomy 21, the chromosomal abnormality causing Down syndrome. Gene expression profiles generated from DNA ...
Abstract Background Cardiac erosion after percutaneous atrial septal defect (ASD) closure is a rare complication that requires immediate life-saving emergency surgery. In this report, we present our successful strategy for cardiac arrest due to tamponade caused by 6 years the of an ASD. Case presentation The patient was 50-year-old man who received treatment using Amplatzer occluder (St. Jude M...
Noonan syndrome is a rare genetic disease with multisystemic manifestations, typically diagnosed in infancy and childhood. This case report presents 53-year-old woman no significant medical history who presented shortness of breath was subsequently syndrome. The patient exhibited characteristic facial dysmorphology, including narrow face, low set ears, pectus excavatum. Physical examination rev...
Introduction: Along with advances occurring in cardiopulmonary bypass (CPB) including improved anesthesia intubation and early surgical interventions, it has become possible to correct life-threatening congenital heart anatomic abnormalities in patients. Our study aimed to collect information from one of the most important centers of pediatric cardiac surgery in Iran since there is limited info...
Percutaneous closure of secundum atrial septal defects (ASD) may be complicated by immediate embolization. We report on a 35-year-old woman who underwent percutaneous device closure for a secundum ASD. The diameter of the defect was measured as 4 mm by two-dimensional transesophageal echocardiography and a 7-mm Figulla ASD occluder device was implanted without prior balloon sizing of the defect...
The case of a 19-year-old female with a neonatal diagnosis of Tetralogy of Fallot and complete atrioventricular (AV) septal defect is described. She had had a corrective surgery at the age of 6. She did well afterwards despite recent complain of fatigability with mild arterial hypoxaemia. Transoesophageal echocardiography depicted a 12 mm atrial septal defect (ASD) with a bidirectional shunt, w...
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