Prenatal diagnosis of 46,XY/46,XX mosaicism: A case report

Citation
Y. Yaron et al., Prenatal diagnosis of 46,XY/46,XX mosaicism: A case report, AM J MED G, 84(1), 1999, pp. 12-14
Citations number
1
Categorie Soggetti
Molecular Biology & Genetics
Journal title
AMERICAN JOURNAL OF MEDICAL GENETICS
ISSN journal
01487299 → ACNP
Volume
84
Issue
1
Year of publication
1999
Pages
12 - 14
Database
ISI
SICI code
0148-7299(19990507)84:1<12:PDO4MA>2.0.ZU;2-C
Abstract
We report on the prenatal diagnosis of a fetus with 46,XY and 46,XX cell li nes with a normal male phenotype, Cytogenetic and molecular studies ruled o ut the possibility of maternal cell contamination and showed that all the X chromosomes present in both fetal cell lines were derived from a single ma ternal X chromosome, This suggests 46,XY/46,XX mosaicism. (C) 1999 Wiley-Li ss, Inc.