Abstract

As medical and surgical management of congenital heart disease in infancy continues to improve, severe and complex defects are increasingly recognized as the source of mortality and long-term morbidity. The asplenia syndrome has a very poor prognosis; indeed, in 1962, Roberts and associates 1 stated that “the finding of asplenia and situs inversus in a patient with congenital heart disease virtually precludes…corrective or even palliative surgical procedures.” As part of a study of embryologic timing of the syndrome, 2 we reviewed 519 autopsy cases in an attempt to define risk factors associated with early unfavorable outcome.

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