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Congenit Heart Dis ; 2(6): 442-5, 2007.
Article in English | MEDLINE | ID: mdl-18377440

ABSTRACT

A male infant presented at birth with severe coarctation of the aorta and marginal left ventricular and mitral valve dimensions associated with a large secundum atrial septal defect. Following successful arch repair, the left ventricle remained small with preferential left-to-right atrial shunting and a dilated right ventricle. Clinically, the infant continued with tachypnea, poor feeding, and failure to thrive. At 4 months of age, the defect was closed with an Amplatzer Atrial Septal Occluder which resulted in immediate left ventricular cavity enlargement and clinical improvement.


Subject(s)
Aortic Coarctation/complications , Heart Septal Defects, Atrial/complications , Heart Septal Defects, Atrial/surgery , Ventricular Dysfunction, Left/congenital , Ventricular Dysfunction, Left/complications , Aortic Coarctation/surgery , Cardiac Catheterization , Echocardiography , Heart Septal Defects, Atrial/diagnosis , Humans , Infant, Newborn , Infant, Premature , Male , Prosthesis Implantation/instrumentation , Prosthesis Implantation/methods , Ventricular Dysfunction, Left/diagnosis
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