DOI: 10.36347/sjmcr.2023.v11i10.010

Pages: 1763-1766

Kartagener syndrome, a very rare genetic disease with autosomal recessive transmission, is described by the triad of bronchiectasis, chronic sinusitis and complete or incomplete situs inversus. This syndrome is part of primary ciliary dyskinesia, it’s characterized by clinical symptoms of respiratory infections or/and infertility. Situs inversus is often discovered incidentally. The diagnosis is confirmed by specialized centers through analysis of ciliary ultrastructure and genetic testing. Treatment is supportive and in accordance with recommendations.