{Reference Type}: Case Reports
{Title}: Late Diagnosis of Kartagener Syndrome in an Adult Female.
{Author}: Tsetsou I;Balomenos V;Koreas P;Biliara IE;Tavernaraki K;
{Journal}: Cureus
{Volume}: 16
{Issue}: 4
{Year}: 2024 Apr
暂无{DOI}: 10.7759/cureus.58747
{Abstract}: Kartagener syndrome (KS), also known as primary ciliary dyskinesia, is a rare genetic disorder commonly diagnosed early in childhood. It is characterized by a triad of findings, namely, situs inversus, chronic sinusitis, and bronchiectasis. Here, we present the case of a 73-year-old female who incidentally presented the KS triad during her imaging tests in the emergency department of our institution for COVID-19 symptoms.