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Absence of the arterial duct in a neonate with tricuspid atresia

Published online by Cambridge University Press:  19 August 2008

Beth Bubolz ,
Christopher L. Case  and
Robert M. Sade
Beth Bubolz*
Affiliation:
From the Medical University of South Carolina, South Carolina Children's Heart Center, Division of Pediatric Cardiology, Charleston, South Carolina
Christopher L. Case
Affiliation:
From the Medical University of South Carolina, South Carolina Children's Heart Center, Division of Pediatric Cardiology, Charleston, South Carolina
Robert M. Sade
Affiliation:
From the Medical University of South Carolina, South Carolina Children's Heart Center, Division of Pediatric Cardiology, Charleston, South Carolina
*
Dr. Beth Bubolz, Medical University of South Carolina,South Carolina Children's Heart Center, Division of Pediatric Cardiology, 171 Ashley Avenue, Charleston, South Carolina 29425, USA. Tel. (803) 792-3300; Fax. (803) 792-3284.
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Summary

Summary Absence of the arterial duct has been reported in association with tetralogy of Fallot, with pulmonary stenosis or atresia, other complex cyanotic congenital heart diseases, and anomalies of the aortic arch but not, as far as we are aware, with tricuspid atresia. We report the clinical, surgical, and autopsy findings of a patient with tricuspid atresia whose initial clinical course was influenced by the absence of thearterial duct.

Keywords

Tricuspid atresiaabsent arterial ductCHARGE
Type
Brief Reports
Information
Cardiology in the Young , Volume 4 , Issue 2 , April 1994 , pp. 187 - 189
Copyright
Copyright © Cambridge University Press 1994

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References

1.Willius, FA. Cardiac clinics. CXXIV: An unusually early description of the so-called tetralogy of Fallot. Proc Staff Meet Mayo Clin 1948; 23: 99–104.Google Scholar
2.Emmanouilides, GC, Thanopoulos, B, Siassi, B, Fishbein, M. “Agenesis” of ductus arreriosus associated with the syndrome of tetralogy of Fallot and absent pulmonary valve. Am J Cardiol 1976; 37: 403–409.Google Scholar
3.Hamilton, WT, Lacina, SJ, Bharati, S, Lev, M, Arcilla, RA. Failure of clinical response to prostaglandin E1 in a cyanotic infant with congenital absence of the ductus arteriosus. Cathet Cardiovasc Diagn 1982; 8: 273–276.CrossRefGoogle Scholar
4.Morgan, JR, Forker, AD, Fosburg, RG, Neugebauer, MK,Rogers, AK, Bemiller, CR. Interruption of the aortic arch without a patent ductus arteriosus. Circulation 1970; 42: 961–965.Google Scholar
5.Salazar, J. Double-inlet left ventricle with absent sixth aortic arch and multiple cardiac malformations. Acta Cardiol 1975; 4: 323–327.Google Scholar
6.Shin, HS, Cho, KJ, Suh, YL, Chi, JG. Congenital absence of ductus arteriosus: An autopsy case. J Korean Med Sci 1988; 3: 41–43.Google Scholar
7.Van Mierop, LHS, Kutsche, LM. Cardiovascular anomalies in DiGeorge syndrome and importance of neural crest as a possible pathogenetic factor. Am J Cardiol 1986; 58: 133–137.Google Scholar
8.Wyse, RKH, Al-Mahdawi, S, Burn, J, Blake, K. Congenital heart disease in CHARGE association. Pediatr Cardiol 1993; 14: 75–81.CrossRefGoogle ScholarPubMed
9.Lacina, SJ, Hamilton, WT, Thilenius, OG, Bharati, S, Lev, M,Arcilla, RA. Angiographic evidence of absent ductus arteriosus in severe right ventricular out flow obstruction. Pediatr Cardiol 1983; 4: 5–11.Google Scholar
10.Knight, L, Edwards, JE. Right aortic arch: Types and associated cardiac anomalies. Circulation 1974; 50: 1047–1051.CrossRefGoogle ScholarPubMed