Congenital heart diseases and cardiovascular abnormalities in 22q11.2 deletion syndrome: From well-established knowledge to new frontiers

Author:

Unolt Marta1ORCID,Versacci Paolo1,Anaclerio Silvia1,Lambiase Caterina1,Calcagni Giulio2,Trezzi Matteo2,Carotti Adriano2,Crowley Terrence Blaine3,Zackai Elaine H.3,Goldmuntz Elizabeth4,Gaynor James William4,Digilio Maria Cristina5ORCID,McDonald-McGinn Donna M.3,Marino Bruno1

Affiliation:

1. Department of Pediatrics and Pediatric Neuropsychiatry; “Sapienza” University of Rome; Rome Italy

2. Department of Pediatric Cardiology and Cardiac Surgery; Bambino Gesù Pediatric Hospital; Rome Italy

3. Division of Human Genetics; The Children's Hospital of Philadelphia; Philadelphia Pennsylvania

4. The Cardiac Center, The Children's Hospital of Philadelphia; Philadelphia Pennsylvania

5. Division of Medical Genetics; Bambino Gesù Pediatric Hospital; Rome Italy

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference157 articles.

1. Pulmonary atresia with ventricular septal defect and persistent airway hyperresponsiveness;Ackerman;The Journal of Thoracic and Cardiovascular Surgery,2001

2. The impact of 22q11.2 deletion syndrome on surgical repair outcomes of conotruncal cardiac anomalies;Alsoufi;Annals of Thoracic Surgery,2017

3. Selective management strategy of interrupted aortic arch mitigates left ventricular outflow tract obstruction risk;Alsoufi;The Journal of Thoracic and Cardiovascular Surgery,2016

4. Conotruncal heart defects: Impact of genetic syndromes on immediate operative mortality;Anaclerio;Italian Heart Journal,2004

5. Pulmonary atresia with ventricular septal defect: Prevalence of deletion 22q11 in the different anatomic patterns;Anaclerio;Italian Heart Journal,2001

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