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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
  • Primary Ciliary Dyskinesia
  • Polynesian Bronchiectasis
  • Bronchiectasis, Polynesian
  • Polynesian Bronchiectases
  • Dextrocardia, Bronchiectasis, and Sinusitis
  • Ciliary Dyskinesia, Primary, 1
  • Ciliary Dyskinesia, Primary, 1, With Or Without Situs Inversus
  • Ciliary Dyskinesia, Primary
  • Dyskinesia, Primary Ciliary
  • Siewert Syndrome
  • Syndrome, Siewert

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