Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Atrial situs inversus"'
Transcript analysis for variant classification resolution in a child with primary ciliary dyskinesia
Autor:
Alexander Ing, Erica Toledo, Theresa A. Laguna, Joel Charrow, Victoria R. Sanders, Kristina Firestein, Mary Kate McIntyre, Sabah Kadri, Dawn A. Kirschmann, Alissa Wlodaver, Joanne Salazar, Kai Lee Yap, Christopher McCabe
Publikováno v:
Cold Spring Harbor Molecular Case Studies
Transcriptional analysis can be utilized to reconcile variants of uncertain significance, particularly those predicted to impact splicing. Laboratory analysis of the predicted mRNA transcript may allow inference of the in vivo impact of the variant a
Publikováno v:
World Journal of Cardiovascular Surgery. :99-103
10-year female child was presented with complex congenital heart defect—atrial situs inversus, levocardia, discordant atrioventricular connections, double outlet right ventricle, ventricular septal defect, pulmonic stenosis and straddling of atrio-
Percutaneous pulmonary valve implantation (PPVI) of bovine valves mounted in a stent (Melody®, Medtronic) has become a well-established therapy in patients with significant dysfunction of conduits between the right ventricle and the pulmonary arteri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::05aea31d4b8d43dba66a8d0a7e0485c4
http://doc.rero.ch/record/298953/files/ehr234.pdf
http://doc.rero.ch/record/298953/files/ehr234.pdf
Autor:
Kristine J. Guleserian, Joseph M. Forbess, Rabih Hamzeh, Amy L. Juraszek, Vinod A. Sebastian, Colin E Kane
Publikováno v:
The Annals of Thoracic Surgery. 100:1446-1448
The Senning and Mustard baffles remain important techniques for the treatment of congenitally corrected transposition (cc-TGA), isolated ventricular inversion, and D-transposition of the great arteries with delayed presentation. We describe the treat
Autor:
Trushar Gajjar, Neelam Desai
Publikováno v:
Turkish Journal of Thoracic and Cardiovascular Surgery. 21:245-249
Displacement of the septum primum-leftward in atrial situs solitus or rightward in atrial situs inversus is termed as septum primum malposition defect. It appears to be responsible for the anomalous pulmonary venous drainage. This abnormality occurs
Autor:
Luca A. Vricella, Steven R. Gundry, Micheal A Kuhn, Ranae L. Larsen, Leonard L. Bailey, Anees J. Razzouk
Publikováno v:
The Journal of Thoracic and Cardiovascular Surgery. 116(1):82-89
Background: Recipient situs inversus has always represented a technical challenge during heart transplantation. Objective: A simplified operative strategy for heart transplantation in a recipient with atrial situs inversus is described. Methods: Fift
Autor:
Saadeh Al-Jureidini, Ian C. Balfour, Andrew C. Fiore, Vinay Tak, Barbara Kountzman, Mary Hohenberg
Publikováno v:
The Annals of Thoracic Surgery. 81:746-748
This report describes the technique to fenestrate the extracardiac Fontan conduit without cardiopulmonary bypass in a patient with levocardia and atrial situs inversus.
Publikováno v:
Congenital heart disease. 5(2)
Objective. Discontinuous pulmonary arteries are believed to portend poor outcomes for a single ventricle palliation leading to Fontan's operation. This is a single institutional review of patients with single ventricle and discontinuous pulmonary art
Autor:
Patricia O’Brien, Aldo R. Castaneda, Ira A. Parness, Antonio R. Perez-Atayde, Stanton B. Perry, John E. Mayer, Richard A. Jonas
Publikováno v:
The Journal of Thoracic and Cardiovascular Surgery. 99:484-492
Orthotopic heart transplantation has become standard therapy for end-stage cardiomyopathy in children and adults, but there has been much less experience with transplantation for complex congenital heart disease. In this report experience with orthot
Autor:
Bruno Reichart, R. Kozlik-Feldmann, Ingo Kaczmarek, Andres Beiras-Fernandez, A.R. Tiete, Sabine Daebritz
Publikováno v:
The Journal of heart and lung transplantation : the official publication of the International Society for Heart Transplantation. 26(3)
Heart transplantation represents a valuable therapeutic option for patients with congenital heart disease and end-stage heart failure. We report the case of a 15-year-old patient with situs inversus and additional complex congenital malformations of