Trisomy 22: prenatal diagnosis--a case report

K Harding; J Freeman; W Weston; J R Smith

doi:10.1046/j.1469-0705.1995.05020136.x

Trisomy 22: prenatal diagnosis--a case report

Ultrasound Obstet Gynecol. 1995 Feb;5(2):136-7. doi: 10.1046/j.1469-0705.1995.05020136.x.

Authors

K Harding¹, J Freeman, W Weston, J R Smith

Affiliation

¹ Department of Obstetrics and Gynaecology, Chelsea and Westminster Hospital, London, UK.

PMID: 7719866
DOI: 10.1046/j.1469-0705.1995.05020136.x

Abstract

Multiple abnormalities of a fetus were detected on a routine antenatal anomaly scan at 19 weeks' gestation. Amniocentesis and karyotype analysis showed trisomy 22. The ultrasound and postmortem features are presented.

Publication types

Case Reports

MeSH terms

Abnormalities, Multiple / diagnostic imaging
Abnormalities, Multiple / genetics
Adult
Amniocentesis
Chromosomes, Human, Pair 22* / genetics
Female
Humans
Karyotyping
Pregnancy
Trisomy / diagnosis*
Trisomy / genetics
Ultrasonography, Prenatal*