Sex chromosome mosaicism not detected at amniocentesis

1 May 1990

journal article
research article
Published by Wiley in Prenatal Diagnosis

Vol. 10 (5) , 333-336
https://doi.org/10.1002/pd.1970100509

Abstract

Amniocentesis was performed because of a fetal abdominal wall defect, and a 45,X karyotype was obtained. A near‐normal male infant with no features of Turner syndrome was delivered. The karyotype of the infant was 45,X/46,X, dic(Y)(q11), with each of the cell lines present in approximately 50 per cent of the lymphocytes and fibroblasts examined.

Keywords

This publication has 9 references indexed in Scilit:

Prenatal diagnosis of 45,X/46,XY mosaicism—A review and update
Prenatal Diagnosis, 1989
45,X/46,XY Mosaicism. Contrast of prenatal and postnatal diagnosis
American Journal of Medical Genetics, 1988
Prenatal diagnosis of 45,X/46,XY mosaicism in a fetus with asymmetric gonadal dysgenesis
Prenatal Diagnosis, 1987
Five cases of prenatally diagnosed sex chromosome mosaicism
Prenatal Diagnosis, 1985
European collaborative study on prenatal diagnosis: Mosaicism, pseudomosaicism and single abnormal cells in amniotic fluid cell cultures
Prenatal Diagnosis, 1984
A canadian collaborative study of mosaicism in amniotic fluid cell cultures
Prenatal Diagnosis, 1984
United states survey on chromosome mosaicism and pseudomosaicism in prenatal diagnosis
Prenatal Diagnosis, 1984
Sex chromosomal mosaicism undetected by prenatal study
The Journal of Pediatrics, 1977
EXCLUSION OF CHROMOSOMAL MOSAICISM - TABLES OF 90PERCENT, 95PERCENT, AND 99PERCENT CONFIDENCE-LIMITS AND COMMENTS ON USE
1977