triploid syndrome
Sign in to saveAlso known as triploidy, chromosome triploidy syndrome, triploidy syndrome
extremely rare chromosomal disorder occuring during human embryogenesis, causing severe abnormalities in fetal development and usually lethal in the prenatal stage
Research
382 papers- Holoprosencephaly.American journal of obstetrics and gynecology · 2020
- Exencephaly-anencephaly Sequence.American journal of obstetrics and gynecology · 2020
- Chromosomal microarray versus karyotyping for prenatal diagnosis.The New England journal of medicine · 2012
- Maternal age and the risk of fetal aneuploidy: A nationwide cohort study of more than 500 000 singleton pregnancies in Denmark from 2008 to 2017.Acta obstetricia et gynecologica Scandinavica · 2024
- [Triploidy syndrome and diploid/triploid mixoploidy syndrome].Ryoikibetsu shokogun shirizu · 2000
via PubMed
Wikidata facts
Show 5 more facts
- ICD-9-CM
- 758.89
- has cause
- triploidy
- exact match
- www.orpha.net/ORDO/Orphanet_3376
- NCI Thesaurus ID
- C85204
- health specialty
- medical genetics
Sources (2)
via Wikidata · CC0