Kartagener Syndrome is a rare genetic disorder that affects the cilia, which are tiny hair-like structures that help move mucus and other substances in the body. People with this condition often experience chronic respiratory issues, such as frequent lung infections and sinusitis, because their cilia do not function properly. This syndrome is part of a group of disorders known as primary ciliary dyskinesia. In addition to respiratory problems, Kartagener Syndrome is characterized by a condition called situs inversus, where the internal organs are mirrored from their normal positions. This can lead to complications in organ function. Early diagnosis and treatment are essential to manage symptoms and improve the quality of life for those affected.