Family Case of The Clinical Course of Cartagener's Syndrome in Children

Kartagener's syndrome (KS) is a rare hereditary disease characterized by a triad of symptoms: primary ciliary dyskinesia, situs inversus, and chronic respiratory infections. This article presents a family case of KS in children, emphasizing the clinical features, diagnostic challenges, and management strategies. The study analyzes the genetic aspects, pathophysiology, and progression of the disease in affected siblings. Special attention is given to respiratory complications, recurrent infections, and the impact on the quality of life. Early diagnosis and comprehensive therapeutic approaches, including airway clearance techniques and antibiotic prophylaxis, are crucial for improving long-term outcomes in children with KS.

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