Kartagener's syndrome is a rare, autosomal recessive genetic ciliary disorder comprising the triad of situs inversus, chronic sinusitis, and bronchiectasis. The basic problem lies in the defective movement of cilia, leading to recurrent chest infections, ear/nose/throat symptoms, and infertility.
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Sep 24, 2024 · Approximately one half of patients with primary ciliary dyskinesia have situs inversus and, thus, are classified as having Kartagener syndrome.
Feb 20, 2024 · Kartagener syndrome is a rare genetic disease that affects the cilia in your lungs and other organs. What Is Kartagener Syndrome?
Kartagener's syndrome is an inherited disease characterized by the clinical triad of bronchiectasis, sinusitis, and situs inversus. The respiratory defect is ...
Jan 12, 2011 · Kartagener syndrome is a rare, ciliopathic, autosomal recessive genetic disorder that causes a defect in the action of the cilia lining the ...
Kartagener syndrome, a rare inherited birth defect, is a type of primary ciliary dyskinesia (PCD), a condition marked by frequent infections of the lungs, ...
Primary ciliary dyskinesia (PCD) is a rare, autosomal recessive genetic ciliopathy, that causes defects in the action of cilia lining the upper and lower ...
What is it? This condition involves recurrent infections usually affecting the lungs, ears and nose which, if left untreated, may lead to long term lung damage.
May 14, 2024 · Kartagener syndrome (also known as Kartagener-Afzelius syndrome) is a subset of primary ciliary dyskinesia, an autosomal recessive condition ...
Jan 10, 2018 · Kartagener's syndrome (KS) is a rare autosomal recessive genetic disorder which was first described by Siewert in 1904; however, Kartagener ...
