"Trisomy 18 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.
A chromosome disorder associated with TRISOMY of all or part of CHROMOSOME 18. Clinical manifestations include INTRAUTERINE GROWTH RETARDATION; CLEFT PALATE; CONGENITAL HEART DEFECTS; MICROCEPHALY; MICROGNATHIA and clenched fists with overlapping fingers. Most affected fetuses do not survive to birth. Those who survive through their first year often have severe INTELLECTUAL DISABILITY.
| Descriptor ID |
D000073842
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| MeSH Number(s) |
C14.240.400.975 C14.280.400.975 C16.131.077.929 C16.131.240.400.968 C16.131.260.932 C16.320.180.932
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| Concept/Terms |
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Below are MeSH descriptors whose meaning is more general than "Trisomy 18 Syndrome".
Below are MeSH descriptors whose meaning is more specific than "Trisomy 18 Syndrome".
This graph shows the total number of publications written about "Trisomy 18 Syndrome" by people in this website by year, and whether "Trisomy 18 Syndrome" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2016 | 0 | 1 | 1 |
| 2018 | 1 | 0 | 1 |
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Below are the most recent publications written about "Trisomy 18 Syndrome" by people in Profiles.
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Sensitivity of prenatal ultrasound for detection of trisomy 18. J Matern Fetal Neonatal Med. 2019 Nov; 32(22):3716-3722.
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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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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.