"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
|
| 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
|
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,
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| Year | Major Topic | Minor Topic | Total |
|---|
| 1998 | 1 | 0 | 1 |
| 2002 | 1 | 0 | 1 |
| 2008 | 1 | 0 | 1 |
| 2010 | 0 | 1 | 1 |
| 2012 | 1 | 1 | 2 |
| 2013 | 1 | 0 | 1 |
| 2017 | 1 | 0 | 1 |
| 2021 | 2 | 0 | 2 |
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Below are the most recent publications written about "Kartagener Syndrome" by people in Profiles.
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Analysis of the clinical features of Japanese patients with primary ciliary dyskinesia. Auris Nasus Larynx. 2022 Apr; 49(2):248-257.
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Left Pulmonary Artery Patch Augmentation for Lung Transplant in a Patient With Situs Inversus. Tex Heart Inst J. 2021 01 01; 48(1).
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Paediatric case of ductal origin of right pulmonary artery presenting with exertional dyspnoea and mimicking asthma and primary ciliary dyskinesia. BMJ Case Rep. 2017 Oct 10; 2017.
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ARMC4 mutations cause primary ciliary dyskinesia with randomization of left/right body asymmetry. Am J Hum Genet. 2013 Aug 08; 93(2):357-67.
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Exhaled breath condensate purines correlate with lung function in infants and preschoolers. Pediatr Pulmonol. 2013 Feb; 48(2):182-7.
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Chest MRI in children: why bother? Respirology. 2012 Jan; 17(1):3-4.
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Clinical course after successful double lung transplantation in a patient with severe scoliosis. J Heart Lung Transplant. 2011 Feb; 30(2):234-5.
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Index of suspicion. Pediatr Rev. 2008 Oct; 29(10):355-61.
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Otolaryngologic manifestations of immunodeficiency. Otolaryngol Clin North Am. 2003 Aug; 36(4):647-72.
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Mutations in the DNAH11 (axonemal heavy chain dynein type 11) gene cause one form of situs inversus totalis and most likely primary ciliary dyskinesia. Proc Natl Acad Sci U S A. 2002 Aug 06; 99(16):10282-6.