Kartagener Syndrome
An autosomal recessive disorder characterized by a triad of DEXTROCARDIA; INFERTILITY; and SINUSITIS. The syndrome is caused by mutations of DYNEIN genes encoding motility proteins which are components of sperm tails, and CILIA in the respiratory and the reproductive tracts.
Year introduced: 2002 (1963)
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Subheadings:
Tree Number(s): C08.127.384.500, C08.200.531, C08.695.501, C09.150.531, C14.240.400.280.500, C14.280.400.280.500, C16.131.077.245.500.531, C16.131.240.400.280.500, C16.131.740.501, C16.131.810.250.500, C16.320.184.500.531, C16.320.480
MeSH Unique ID: D007619
Entry Terms:
- Syndrome, Kartagener
- Kartagener's Syndrome
- Kartageners Syndrome
- Syndrome, Kartagener's
- Kartagener's Triad
- Kartageners Triad
- Kartagener Triad
- Siewert Syndrome
- Syndrome, Siewert
- Dextrocardia, Bronchiectasis, and Sinusitis
- Ciliary Dyskinesia, Primary, 1
- Ciliary Dyskinesia, Primary, 1, With Or Without Situs Inversus
- Polynesian Bronchiectasis
- Bronchiectasis, Polynesian
- Polynesian Bronchiectases