Literature DB >> 2245116

Aortic atresia: survival to adulthood without surgery.

P Maxwell1, J Somerville.   

Abstract

Aortic atresia is a rare congenital cardiac defect. It usually leads to death in the neonatal period. A patient with aortic atresia has survived to the age of 24 years without any surgical procedure. In view of the uncertain results of reconstructive surgery this case may have therapeutic implications.

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Year:  1990        PMID： 2245116      PMCID： PMC1216816          DOI： 10.1136/hrt.64.5.336

Source DB:  PubMed          Journal:  Br Heart J        ISSN： 0007-0769


  5 in total

1.  The hypoplastic left heart syndrome; an analysis of 101 cases.

Authors:  J A NOONAN; A S NADAS
Journal:  Pediatr Clin North Am       Date:  1958-11       Impact factor: 3.278

2.  Pathologic anatomy and interrelationship of hypoplasia of the aortic tract complexes.

Authors:  M LEV
Journal:  Lab Invest       Date:  1952       Impact factor: 5.662

3.  Congenital aortic atresia. Report of long survival and some speculations about surgical approaches.

Authors:  D S Moodie; W J Gallen; D Z Friedberg
Journal:  J Thorac Cardiovasc Surg       Date:  1972-05       Impact factor: 5.209

4.  Physiologic repair of aortic atresia-hypoplastic left heart syndrome.

Authors:  W I Norwood; P Lang; D D Hansen
Journal:  N Engl J Med       Date:  1983-01-06       Impact factor: 91.245

5.  Conal anatomy in aortic atresia, ventricular septal defect, and normally developed left ventricle.

Authors:  R M Freedom; M R Dische; R D Rowe
Journal:  Am Heart J       Date:  1977-12       Impact factor: 4.749
  5 in total
  2 in total

1.  Stenting the arterial duct.

Authors:  J L Gibbs
Journal:  Arch Dis Child       Date:  1995-03       Impact factor: 3.791

2.  Developments in interventional cardiac catheterisation and progress in surgery for congenital heart disease: achieving a balance.

Authors:  S A Qureshi; M Tynan
Journal:  Br Heart J       Date:  1993-07
  2 in total

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