Literature DB >> 18396220

Thoracic aortic aneurysm syndrome in children.

Giorgio Zanotti1, Luca Vricella, Duke Cameron.   

Abstract

In contrast with adults, thoracic aortic aneurysms in children are usually associated with connective tissue defect syndromes. As such, there are phenotypic clues to identify patients at risk. Marfan syndrome, Loeys-Dietz syndrome, and bicuspid aortic valve syndrome account for the majority of these aneurysms. Indications for surgery as well as surgical options differ according to diagnosis and are reviewed herein.

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Year:  2008        PMID: 18396220     DOI: 10.1053/j.pcsu.2008.01.005

Source DB:  PubMed          Journal:  Semin Thorac Cardiovasc Surg Pediatr Card Surg Annu        ISSN: 1092-9126


  6 in total

1.  Impact of asymmetry on measurements of the aortic root using cardiovascular magnetic resonance imaging in patients with a bicuspid aortic valve.

Authors:  Felipe S Torres; Jonathan D Windram; Timothy J Bradley; Bernd J Wintersperger; Ravi Menezes; Andrew M Crean; Jack M Colman; Candice K Silversides; Rachel M Wald
Journal:  Int J Cardiovasc Imaging       Date:  2013-08-02       Impact factor: 2.357

2.  Canadian Cardiovascular Society 2009 Consensus Conference on the management of adults with congenital heart disease: outflow tract obstruction, coarctation of the aorta, tetralogy of Fallot, Ebstein anomaly and Marfan's syndrome.

Authors:  Candice K Silversides; Marla Kiess; Luc Beauchesne; Timothy Bradley; Michael Connelly; Koichiro Niwa; Barbara Mulder; Gary Webb; Jack Colman; Judith Therrien
Journal:  Can J Cardiol       Date:  2010-03       Impact factor: 5.223

3.  Abnormal Longitudinal Growth of the Aorta in Children with Familial Bicuspid Aortic Valve.

Authors:  Holly Nadorlik; Jessica L Bowman; Sara Fitzgerald-Butt; May Ling Mah; Kim L McBride; John P Kovalchin; Vidu Garg
Journal:  Pediatr Cardiol       Date:  2017-09-25       Impact factor: 1.655

4.  Tetralogy of Fallot and aortic root dilation: a long-term outlook.

Authors:  Christian D Nagy; Diane E Alejo; Mary C Corretti; William J Ravekes; Jane E Crosson; Philip J Spevak; Richard Ringel; Kathryn A Carson; Sara Khalil; Harry C Dietz; Duke E Cameron; Luca A Vricella; Thomas A Traill; Kathryn W Holmes
Journal:  Pediatr Cardiol       Date:  2012-10-19       Impact factor: 1.655

5.  A Newly Discovered Genetic Disorder Associated With Life-Threatening Aortic Disease in a 6-Year-Old Boy.

Authors:  Mohanad Hamandi; Madison L Bolin; Joy Fan; Allison T Lanfear; Seth K Woolbert; Ronald D Baxter; J Michael DiMaio; William T Brinkman
Journal:  J Investig Med High Impact Case Rep       Date:  2020 Jan-Dec

6.  Pulmonary artery rupture after bilateral pulmonary artery banding in a neonate with Loeys-Dietz syndrome and an interrupted aortic arch complex: report of a case.

Authors:  Hideto Ozawa; Hiroaki Kawata; Shigemitsu Iwai; Sanae Yamauchi; Tomomitsu Kanaya; Hidefumi Kishimoto
Journal:  Surg Today       Date:  2014-05-11       Impact factor: 2.549

  6 in total

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