Structured Summary
Abstract
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.
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Classification
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MeSH Record
Synonyms
6 entry terms
- Trisomy 18 Syndromes
- Complete Trisomy 18 Syndrome
- Edwards Syndrome
- Mosaic Trisomy 18 Syndrome
- Trisomy 18
- Trisomy E Syndrome
MeSH Record
Aspects Covered
34 allowable subheadings
Indexed with the subheadings blood, cerebrospinal fluid, chemically induced, classification, complications, diagnosis, diagnostic imaging, diet therapy, drug therapy, economics, embryology, enzymology, epidemiology, ethnology, etiology, genetics, history, immunology, metabolism, microbiology, mortality, nursing, parasitology, pathology, physiopathology, prevention & control, psychology, radiotherapy, rehabilitation, surgery, therapy, urine, veterinary, virology.
MeSH Record
History Note
2018
MeSH Hierarchy
Tree Numbers
AMA Style
References
- National Library of Medicine. Trisomy 18 Syndrome. Medical Subject Headings (MeSH). 2026. Unique ID D000073842. http://id.nlm.nih.gov/mesh/2026/D000073842
- Trisomy 18 Syndrome. In: Wikipedia. https://en.wikipedia.org/wiki/Trisomy_18
- Trisomy 18 Syndrome. In: Wikidata. https://www.wikidata.org/wiki/Q457737