KARTAGENER'S SYNDROME: A CASE REPORT

Area of Science:

• Medical Genetics
• Pulmonology
• Otolaryngology

Background:

• Kartagener's syndrome is a rare autosomal recessive genetic disorder characterized by defective cilia function.
• This defect impacts mucociliary clearance in the respiratory tract, leading to chronic infections.

Observation:

• A case report of a 12-year-old female presenting with symptoms consistent with Kartagener's syndrome.
• The patient was treated at Tikur Anbessa Teaching Hospital.

Findings:

• The case represents the first documented instance of Kartagener's syndrome in Ethiopia.
• Clinical and imaging findings were analyzed to understand the syndrome's presentation.

Implications:

• This report expands the geographical understanding of Kartagener's syndrome prevalence.
• It underscores the importance of recognizing this rare condition for timely diagnosis and management in diverse populations.