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An infant with transposition and cystic fibrosis

Published online by Cambridge University Press:  02 December 2008

Amanda L. Cook ,
Kari L. Crawford  and
Derek A. Williams
Amanda L. Cook*
Affiliation:
Department of Pediatrics, Division of Pediatric Cardiology, Wake Forest, University School of Medicine, Winston-Salem, North Carolina, United States of America
Kari L. Crawford
Affiliation:
Department of Pediatrics, Division of Pediatric Cardiology, Wake Forest, University School of Medicine, Winston-Salem, North Carolina, United States of America
Derek A. Williams
Affiliation:
Department of Pediatrics, Division of Pediatric Cardiology, Wake Forest, University School of Medicine, Winston-Salem, North Carolina, United States of America
*
Correspondence to: Amanda L. Cook, MD, Wake Forest University School of Medicine, Medical Center Boulevard, Winston-Salem, NC 27157, United States of America. Tel: (336) 716 3232; Fax: (336) 716 0533; E-mail: [email protected]
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Abstract

We report an infant with transposition, with the circumflex artery arising from the right coronary artery, who was diagnosed with cystic fibrosis following the occurrence of meconium ileus in the postoperative period.

Keywords

Congenital heart diseasegenetic syndromesmeconium ileus
Type
Brief Report
Information
Cardiology in the Young , Volume 19 , Issue 1 , February 2009 , pp. 111 - 112
Copyright
Copyright © Cambridge University Press 2008

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References

1. Davis, PB. Cystic fibrosis since 1938. Am J Respir Crit Care Med 2006; 173: 475–482.CrossRefGoogle ScholarPubMed
2. Orenstein, D, Rosenstein, B, Stern, R. Diagnosis of cystic fibrosis. In: Orenstein D, Rosenstein B, Stern R (eds). Cystic fibrosis medical care. Lippincott Williams & Wilkins, Philadelphia, 2000, pp 21–54.Google Scholar
3. Accurso, FJ. Update in cystic fibrosis 2006. Am J Respir Crit Care Med 2007; 175: 754–757.CrossRefGoogle ScholarPubMed
4. Hoffman, JI. Incidence of congenital heart disease: I. Postnatal incidence. Pediatr Cardiol 1995; 16: 103–113.CrossRefGoogle ScholarPubMed
5. Goldmuntz, E, Clark, BJ, Mitchell, LE, et al. Frequency of 22q11 deletions in patients with conotruncal defects. J Am Coll Cardiol 1998; 32: 492–498.CrossRefGoogle ScholarPubMed
6. Balci, S, Haytoglu, T, Ozer, S. A case of a four-day-old male with Carpenter’s syndrome with transposition of great arteries. Turk J Pediatr 1998; 40: 461–466.Google ScholarPubMed
7. Goldmuntz, E, Bamford, R, Karkera, JD, de la Cruz, J, Roessler, E, Muenke, M. CFC1 mutations in patients with transposition of the great arteries and double-outlet right ventricle. Am J Hum Genet 2002; 70: 776–780.CrossRefGoogle ScholarPubMed
8. Muncke, N, Jung, C, Rudiger, H, et al. Missense mutations and gene interruption in PROSIT240, a novel TRAP240-like gene, in patients with congenital heart defect (transposition of the great arteries). Circulation 2003; 108: 2843–2850.CrossRefGoogle ScholarPubMed
9. Digilio, MC, Casey, B, Toscano, A, et al. Complete transposition of the great arteries: patterns of congenital heart disease in familial precurrence. Circulation 2001; 104: 2809–2814.CrossRefGoogle ScholarPubMed
10. Baslaim, GM, Jamjoom, AA. Extracorporeal membrane oxygenation support post-arterial switch procedure for a child with cystic fibrosis: case report. J Card Surg 2006; 21: 419–420.CrossRefGoogle ScholarPubMed