 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 C16.131.077.245.500.531 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.
To see the data from this visualization as text, click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2005 | 1 | 0 | 1 | | 2007 | 0 | 1 | 1 | | 2010 | 0 | 1 | 1 | | 2011 | 2 | 0 | 2 | | 2012 | 1 | 0 | 1 | | 2013 | 5 | 0 | 5 | | 2014 | 2 | 0 | 2 | | 2015 | 2 | 0 | 2 | | 2016 | 3 | 0 | 3 | | 2018 | 1 | 0 | 1 | | 2019 | 1 | 0 | 1 | | 2022 | 1 | 0 | 1 | | 2023 | 3 | 1 | 4 | | 2024 | 1 | 1 | 2 | | 2025 | 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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Barber AT, Davis SD, Ferkol TW, Shapiro AJ, Atkinson J, Sagel SD, Dell SD, Olivier K, Milla C, Rosenfeld M, Li L, Lin FC, Sullivan KM, Capps NA, Zariwala MA, Knowles MR, Leigh MW. The Association of Neonatal Respiratory Distress With Ciliary Ultrastructure and Genotype in Primary Ciliary Dyskinesia. Pediatr Pulmonol. 2025 May; 60(5):e71091.
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Muhonen EG, Zhu A, Sempson S, Bothwell S, Sagel SD, Chan KH. Management of middle ear disease in pediatric primary ciliary dyskinesia. Int J Pediatr Otorhinolaryngol. 2025 May; 192:112297.
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Kinghorn B, Rosenfeld M, Sullivan E, Onchiri FM, Brown MD, Szczesniak R, Ferkol TW, Sagel SD, Dell SD, Milla C, Shapiro AJ, Sullivan KM, Zariwala MA, Pittman JE, Knowles MR, Davis SD, Leigh MW. Comparison of Longitudinal Outcomes in Children with Primary Ciliary Dyskinesia and Cystic Fibrosis. Ann Am Thorac Soc. 2024 Dec; 21(12):1723-1732.
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Gardner RA, Ferkol TW, Davis SD, Rosenfeld M, Sagel SD, Dell SD, Milla CE, Li L, Lin FC, Sullivan KM, Zariwala MA, Knowles MR, Leigh MW. Therapies Used by Children With Primary Ciliary Dyskinesia: A Natural History Study. Pediatr Pulmonol. 2025 Jan; 60(1):e27412.
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Kaspy KR, Dell SD, Davis SD, Ferkol TW, Rosenfeld M, Sagel SD, Milla C, Olivier KN, Barber AT, Wee W, Lin FC, Li L, Rampakakis E, Zariwala MA, Knowles MR, Leigh MW, Shapiro AJ. Situs Ambiguus Is Associated With Adverse Clinical Outcomes in Children With Primary Ciliary Dyskinesia. Chest. 2024 May; 165(5):1070-1081.
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Gardner RA, Sagel SD, Knowles MR, Ferkol TW, Davis SD, Leigh MW, Zariwala MA. Decoding negative genetic panels in primary ciliary dyskinesia. Pediatr Pulmonol. 2024 Mar; 59(3):784-787.
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Kinghorn B, Rosenfeld M, Sullivan E, Onchiri F, Ferkol TW, Sagel SD, Dell SD, Milla C, Shapiro AJ, Sullivan KM, Zariwala MA, Pittman JE, Mollica F, Tiddens HAWM, Kemner-van de Corput M, Knowles MR, Davis SD, Leigh MW. Airway Disease in Children with Primary Ciliary Dyskinesia: Impact of Ciliary Ultrastructure Defect and Genotype. Ann Am Thorac Soc. 2023 04; 20(4):539-547.
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Barber AT, Shapiro AJ, Davis SD, Ferkol TW, Atkinson JJ, Sagel SD, Dell SD, Olivier KN, Milla CE, Rosenfeld M, Li L, Lin FC, Sullivan KM, Capps NA, Zariwala MA, Knowles MR, Leigh MW. Laterality Defects in Primary Ciliary Dyskinesia: Relationship to Ultrastructural Defect or Genotype. Ann Am Thorac Soc. 2023 03; 20(3):397-405.
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Wee WB, Leigh MW, Davis SD, Rosenfeld M, Sullivan KM, Sawras MG, Ferkol TW, Knowles MR, Milla C, Sagel SD, Zariwala MA, Pullenayegum E, Dell SD. Association of Neonatal Hospital Length of Stay with Lung Function in Primary Ciliary Dyskinesia. Ann Am Thorac Soc. 2022 11; 19(11):1865-1870.
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Davis SD, Rosenfeld M, Lee HS, Ferkol TW, Sagel SD, Dell SD, Milla C, Pittman JE, Shapiro AJ, Sullivan KM, Nykamp KR, Krischer JP, Zariwala MA, Knowles MR, Leigh MW. Primary Ciliary Dyskinesia: Longitudinal Study of Lung Disease by Ultrastructure Defect and Genotype. Am J Respir Crit Care Med. 2019 01 15; 199(2):190-198.
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