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Congenitally corrected transposition and degenerative severe aortic stenosis

Published online by Cambridge University Press:  28 August 2008

Giorgio Faganello*
Affiliation:
Adult Congenital Heart Disease Unit, Bristol Royal Infirmary, Bristol, United Kingdom
Martin Nelson
Affiliation:
Adult Congenital Heart Disease Unit, Bristol Royal Infirmary, Bristol, United Kingdom
Graham Stuart
Affiliation:
Adult Congenital Heart Disease Unit, Bristol Royal Infirmary, Bristol, United Kingdom
*
Correspondence to: Giorgio Faganello, MD, Bristol Congenital Heart Disease Unit, Bristol Royal Infirmary, Dolphin House, King Edward Building, Upper Maudlin Street, Bristol, BS2 8BJ, United Kingdom. Tel: +44 (0)1173 420 457; Fax: +44 (0)1173 420 472; E-mail: [email protected]

Abstract

Congenitally corrected transposition is a rare cardiac anomaly characterized by the combination of discordant atrioventricular and ventriculoarterial connections. Young patients with this lesion can present with congestive cardiac failure, usually secondary to a large ventricular septal defect or pulmonary stenosis. We report here our experience with a lady aged 79, admitted to our unit because of deterioration of her congestive cardiac failure as a consequence of uncorrected congenitally corrected transposition associated with degenerative severe aortic stenosis.

Type
Brief Report
Copyright
Copyright © Cambridge University Press 2008

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References

1. Freedom, RM, Dyck, JD. Congenitally corrected transposition of the great arteries. In: Emmanouilides, GC, Riemenschneider, TA, Allen, HD, Gutgesell, HD (eds). Moss and Adams Heart Disease in Infants, Children and Adolescents. 5th edn. Vol. II. Williams and Wilkins, Baltimore, 1995, pp 12251245.Google Scholar
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