Kartagener Syndrome. Situs inversus, bronchiectasia, and diffuse. Kartagener syndrome is a rare, ciliopathic, autosomal recessive genetic disorder that causes a defect in the action of the cilia lining the respiratory tract and.
Kartagener syndrome signs and symptoms vary but may include neonatal respiratory distress; Kartagener syndrome is an autosomal recessive disorder that is characterized by thoracic and abdominal situs inversus as well as the presence of immotile cilia that predispose to sinusitis,. Kartagener's syndrome is a rare disorder involving the combination of situs inversus, bronchiectasis and sinusitis.
Kartagener Syndrome Photograph by Zephyr/science Photo Library
Kartagener syndrome is a rare, ciliopathic, autosomal recessive genetic disorder that causes a defect in the action of the cilia lining the respiratory tract and. Situs inversus, bronchiectasia, and diffuse. Imaging showed bronchiectasis, situs inversus totalis, and sinusitis, findings consistent with. Kartagener's syndrome is a rare disorder involving the combination of situs inversus, bronchiectasis and sinusitis.
