At 28th week of gestation a conotruncal malformation with ventricular septal defect was diagnosed by fetal echocardiography. Postnatal echocardiographic and angiocardiographic examinations confirmed the diagnosis of conotruncal malformation (pulmonary atresia, ventricular septal defect, patent ductus arteriosus, aortopulmonary collateral arteries). The unifocalization (age: 11 months) and total correction with aortic homograft (age: 7 years) were performed. To our knowledge our case is the first whose intrauterine diagnosis of complex congenital heart disease was confirmed after delivery and had successful two-stage surgical management.
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BMC Med Educ
December 2024
Department of Ultrasound, First Affiliated Hospital of Anhui Medical University, No. 218 Jixi Road, Shushan Hefei, Anhui, 230022, China.
Objective: This study aimed to explore the effectiveness of combining fetal heart sequential cross-sectional scanning with drawing methods, mind mapping, and case-based learning (CBL) for training in fetal conotruncal anomalies (CA) screening.
Method: An experimental control method was employed. Doctors participating in continuing fetal ultrasound education were randomly divided into two groups.
Am J Med Genet A
October 2024
Department of Pediatrics, Tohoku University Graduate School of Medicine, Sendai, Japan.
Conotruncal heart defects are severe congenital malformations of the outflow tract, including truncus arteriosus (TA) and double-outlet right ventricle (DORV). TA is a severe congenital heart disease (CHD) in which the main arterial outflow tract of the heart fails to separate. We recently reported TMEM260 (NM_017799.
View Article and Find Full Text PDFBirth Defects Res
October 2024
Department of Neonatology, Cleveland Clinic Children's, Cleveland, Ohio, USA.
Tunis Med
September 2024
Department of Pediatrics and Neonatology, Mongi Slim Hospital, La Marsa, Tunis, Tunisia. University of Tunis el Manar Faculty of Medicine of Tunis.
Introduction: Congenital heart disease is a heterogeneous group of malformations and one of the most common causes of mortality in children.
Aim: The aim of this study was to investigate the clinical, genetic and evolutive characteristics of congenital heart disease.
Methods: A retrospective, descriptive study was carried out between 2020 and 2023 at the pediatrics and neonatology department of Mongi Slim university hospital of Tunis.
J Clin Med
August 2024
Department of Clinical Physiology, Faculty of Medicine, Medical University of Lodz, Mazowiecka 6/8, 92-215 Lodz, Poland.
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