Kartagener's syndrome with corrected transposition. Conducting system studies and coronary arterial occlusion complicating valvular replacement

M. H. Solomon, K. J. Winn, R. D. White, B. H. Bulkley, D. T. Kelly, V. L. Gott, G. M. Hutchins

Research output: Contribution to journalArticlepeer-review

Abstract

An 18 yr old man whose sister has Kartagener's syndrome was found to have sinusitis, bronchiectasis, and corrected transposition with normal visceral situs. Congenital complete heart block was secondary to absence of conducting system pathways between a small posterior atrioventricular node and the transposed His bundle and bundle branches. No anterior atrioventricular node was present. Prosthetic valvular replacement of the left sided (morphologic right) atrioventricular valve was complicated by coronary arterial occlusion by suture, with subsequent myocardial infarction. The case appears to represent an unusual variant of Kartagener's syndrome with the abnormality of laterality being expressed as corrected transposition.

Original languageEnglish (US)
Pages (from-to)677-680
Number of pages4
JournalUnknown Journal
Volume69
Issue number5
DOIs
StatePublished - 1976
Externally publishedYes

ASJC Scopus subject areas

  • Pulmonary and Respiratory Medicine
  • Critical Care and Intensive Care Medicine
  • Cardiology and Cardiovascular Medicine

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