"Kartagener Syndrome" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
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.
| Descriptor ID |
D007619
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| MeSH 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
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| Concept/Terms |
Kartagener Syndrome- Kartagener Syndrome
- Syndrome, Kartagener
- Kartagener's Syndrome
- Kartageners Syndrome
- Syndrome, Kartagener's
- Dextrocardia, Bronchiectasis, and Sinusitis
- Kartagener Triad
- Siewert Syndrome
- Syndrome, Siewert
- Ciliary Dyskinesia, Primary
- Dyskinesia, Primary Ciliary
- Kartagener's Triad
- Kartageners Triad
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Below are MeSH descriptors whose meaning is more general than "Kartagener Syndrome".
Below are MeSH descriptors whose meaning is more specific than "Kartagener Syndrome".
This graph shows the total number of publications written about "Kartagener Syndrome" by people in this website by year, and whether "Kartagener Syndrome" was a major or minor topic of these publications.
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Below are the most recent publications written about "Kartagener Syndrome" by people in Profiles.
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Next generation massively parallel sequencing of targeted exomes to identify genetic mutations in primary ciliary dyskinesia: implications for application to clinical testing. Genet Med. 2011 Mar; 13(3):218-29.