Results 271 to 280 of about 92,272 (308)

Distal aortic remodeling using endovascular repair in acute DeBakey I aortic dissection.

Seminars in Thoracic and Cardiovascular Surgery, 2009
DeBakey type I aortic dissections pose significant challenges in operative and long-term management of the arch and distal thoracic aorta. Concerns regarding management of complex tears extending to the arch and descending thoracic aorta, malperfusion ...
N. Desai, A. Pochettino
semanticscholar   +1 more source

Five syndromes (malformation complexes) of pulmonary symmetry, congenital heart disease, and multiple spleens.

Pediatric Pathology, 1984
The most common multiple anomaly complex with pulmonary isomerism and congenital heart disease is the Ivemark asplenia syndrome.’ Regular features of this disorder include: pulmonary isomerism of right lung type, with three lobar bronchi in each lung ...
B. Landing
semanticscholar   +1 more source

Cardiac defects and results of cardiac surgery in 22q11.2 deletion syndrome.

Developmental Disabilities Research Reviews, 2008
Specific types and subtypes of cardiac defects have been described in children with 22q11.2 deletion syndrome as well as in other genetic syndromes. The conotruncal heart defects occurring in patients with 22q11.2 deletion syndrome include tetralogy of ...
A. Carotti, M. Digilio, G. Piacentini, Claudia Saffirio, R. D. Di Donato, B. Marino   +5 more
semanticscholar   +1 more source

Aortic Arch Management During Acute and Subacute Type A Aortic Syndromes.

Annals of Thoracic Surgery, 2022
Parthavkumar Patel, Andy Dong, Edward Chiou, Jane W. Wei, Jose Binongo, B. Leshnower, E. Chen   +6 more
semanticscholar   +1 more source

Penoscrotal transposition and associated anomalies: report of five new cases and review of the literature.

American journal of medical genetics, 1995
We present the largest single series of cases (n = 5) of penoscrotal transposition (PST) with carefully documented nongenitourinary/anal anomalies, none of which fell into categories of known syndromes, associations, sequences or chromosome disorders ...
S. Parida, B. Hall, L. Barton, A. Fujimoto   +3 more
semanticscholar   +1 more source

Aortic arch syndromes; a survey of five cases.

Acta Medica Scandinavica, 2009
J. Burstein, B. Lindstrom, C. Wasastjerna   +2 more
semanticscholar   +1 more source

Perioperative and Anesthetic Considerations in Interrupted Aortic Arch

Seminars in Cardiothoracic and Vascular Anesthesia, 2018
Nelson H. Burbano-Vera, Katherine L. Zaleski, Gregory J. Latham, V. Nasr   +3 more
semanticscholar   +1 more source

Laterality of the aortic arch and anomalies of the subclavian artery—reliable indicators for 22q11.2 deletion syndromes?

European Journal of Pediatrics, 2004
R. Rauch, A. Rauch, A. Koch, S. Zink, R. Kaulitz, M. Girisch, H. Singer, M. Hofbeck   +7 more
semanticscholar   +1 more source

The Value of Aortic Valve and Aortic Arch Imaging in the Identification of Genetic Syndromes

Echocardiography, 1996
A. Lin
semanticscholar   +1 more source

Right Cervical Aortic Arch and Pseudocoarctation of the Aorta Associated with Aneurysms and Steal Phenomena: US, CTA, and MRA Findings

Cardiovascular and Interventional Radiology, 2007
S. Tanju, E. Ustuner, I. Erden, S. Aytaç   +3 more
semanticscholar   +1 more source