 Kartagener Syndrome
"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 C16.131.240.400.280.500 C16.131.740.501 C16.131.810.250.500 C16.320.480
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| Concept/Terms |
Kartagener Syndrome- Kartagener Syndrome
- Syndrome, Kartagener
- Ciliary Dyskinesia, Primary, 1
- Ciliary Dyskinesia, Primary, 1, With Or Without Situs Inversus
- Dextrocardia, Bronchiectasis, and Sinusitis
- Primary Ciliary Dyskinesia
- Kartagener's Syndrome
- Kartageners Syndrome
- Syndrome, Kartagener's
- Kartagener's Triad
- Kartageners Triad
- Polynesian Bronchiectasis
- Bronchiectasis, Polynesian
- Polynesian Bronchiectases
- Siewert Syndrome
- Syndrome, Siewert
- Ciliary Dyskinesia, Primary
- Dyskinesia, Primary Ciliary
- Kartagener 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.
To see the data from this visualization as text, click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2010 | 0 | 2 | 2 | | 2015 | 1 | 0 | 1 | | 2016 | 1 | 0 | 1 |
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Below are the most recent publications written about "Kartagener Syndrome" by people in Profiles.
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Li Y, Yagi H, Onuoha EO, Damerla RR, Francis R, Furutani Y, Tariq M, King SM, Hendricks G, Cui C, Saydmohammed M, Lee DM, Zahid M, Sami I, Leatherbury L, Pazour GJ, Ware SM, Nakanishi T, Goldmuntz E, Tsang M, Lo CW. DNAH6 and Its Interactions with PCD Genes in Heterotaxy and Primary Ciliary Dyskinesia. PLoS Genet. 2016 Feb; 12(2):e1005821.
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Adams PS, Tian X, Zahid M, Khalifa O, Leatherbury L, Lo CW. Establishing normative nasal nitric oxide values in infants. Respir Med. 2015 Sep; 109(9):1126-30.
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Becker-Heck A, Zohn IE, Okabe N, Pollock A, Lenhart KB, Sullivan-Brown J, McSheene J, Loges NT, Olbrich H, Haeffner K, Fliegauf M, Horvath J, Reinhardt R, Nielsen KG, Marthin JK, Baktai G, Anderson KV, Geisler R, Niswander L, Omran H, Burdine RD. The coiled-coil domain containing protein CCDC40 is essential for motile cilia function and left-right axis formation. Nat Genet. 2011 Jan; 43(1):79-84.
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Swisher M, Jonas R, Tian X, Lee ES, Lo CW, Leatherbury L. Increased postoperative and respiratory complications in patients with congenital heart disease associated with heterotaxy. J Thorac Cardiovasc Surg. 2011 Mar; 141(3):637-44, 644.e1-3.
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