"Trisomy" 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.
The possession of a third chromosome of any one type in an otherwise diploid cell.
Descriptor ID |
D014314
|
MeSH Number(s) |
C23.550.210.050.750 C23.550.210.182.500 G05.365.590.175.050.750 G05.365.590.175.183.500 G05.700.131.750
|
Concept/Terms |
Trisomy- Trisomy
- Trisomies
- Chromosomal Triplication
- Chromosomal Triplications
Partial Trisomy- Partial Trisomy
- Partial Trisomies
- Trisomies, Partial
- Trisomy, Partial
|
Below are MeSH descriptors whose meaning is more general than "Trisomy".
Below are MeSH descriptors whose meaning is more specific than "Trisomy".
This graph shows the total number of publications written about "Trisomy" by people in this website by year, and whether "Trisomy" was a major or minor topic of these publications.
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click here.
Year | Major Topic | Minor Topic | Total |
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1996 | 1 | 0 | 1 |
2005 | 1 | 0 | 1 |
2009 | 0 | 1 | 1 |
2016 | 1 | 1 | 2 |
2017 | 0 | 1 | 1 |
2018 | 0 | 1 | 1 |
2019 | 0 | 1 | 1 |
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Below are the most recent publications written about "Trisomy" by people in Profiles.
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Infantile Epithelioid Sarcoma with Genomic Segmental Amplification of BIRC3/YAP1 as Double Minutes Plus Trisomy 2: A Case Report. Fetal Pediatr Pathol. 2020 Feb; 39(1):51-61.
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Microphthalmia, Dermal Aplasia, and Sclerocornea Syndrome: Endoscopic Cyclophotocoagulation in the Management of Congenital Glaucoma. J Glaucoma. 2018 01; 27(1):e7-e10.
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Rare X Chromosome Abnormalities in Systemic Lupus Erythematosus and Sjögren's Syndrome. Arthritis Rheumatol. 2017 11; 69(11):2187-2192.
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Trisomy 18: A survey of opinions, attitudes, and practices of neonatologists. Am J Med Genet A. 2016 10; 170(10):2638-43.
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X Chromosome Dose and Sex Bias in Autoimmune Diseases: Increased Prevalence of 47,XXX in Systemic Lupus Erythematosus and Sjögren's Syndrome. Arthritis Rheumatol. 2016 05; 68(5):1290-1300.
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Patient choice and clinical outcomes following positive noninvasive prenatal screening for aneuploidy with cell-free DNA (cfDNA). Prenat Diagn. 2016 May; 36(5):456-62.
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Trisomy 18: A single-center evaluation of management trends and experience with aggressive obstetric or neonatal intervention. Am J Med Genet A. 2016 Apr; 170A(4):838-46.
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Papillary renal cell carcinoma with smooth muscle rich stroma: a case report. Pathology. 2012 Aug; 44(5):482-5.
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Primary central nervous system mucosa-associated lymphoid tissue lymphoma: case report and literature review. Clin Lymphoma Myeloma. 2009 Jun; 9(3):E5-9.
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Trisomy 1q in a patient with severe aplastic anemia. Cancer Genet Cytogenet. 2006 Aug; 169(1):73-5.