Literature DB >> 1689816

Tetralogy of Fallot.

W W Pinsky1, E Arciniegas.   

Abstract

Tetralogy of Fallot is the most common malformation of children born with cyanotic heart disease, with an incidence of approximately 10 per cent of congenital heart disease. There can be a wide spectrum as to the severity of the anatomic defects, which include ventricular septal defect, aortic override, right ventricular outflow tract obstruction, and right ventricular hypertrophy. Cyanosis may vary from mild to severe, and patients may present as newborns or, more commonly, young infants. Infants with classic tetralogy of Fallot and stable anatomy should undergo primary complete intracardiac repair. The overall hospital mortality is approximately 3 to 5 per cent, with most patients who survive having an excellent clinical and hemodynamic result.

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Year:  1990        PMID: 1689816     DOI: 10.1016/s0031-3955(16)36839-0

Source DB:  PubMed          Journal:  Pediatr Clin North Am        ISSN: 0031-3955            Impact factor:   3.278


  2 in total

1.  Survival to the age of 87 years in a woman with unoperated tetralogy of Fallot.

Authors:  Ty K Subhawong; Oleg Teytelboym
Journal:  J Radiol Case Rep       Date:  2009-08-01

2.  The myocardial profile of the cytosolic isozymes of creatine kinase is apparently not related to cyanosis in congenital heart disease.

Authors:  G Kessler-Icekson; E Birk; H Schlesinger; Y Barhum; N Ad; M Friedman; B A Vidne
Journal:  Mol Med       Date:  1999-02       Impact factor: 6.354

  2 in total

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