Prenatal application of fluorescent in situ hybridization (FISH) for identification of a mosaic Y-chromosome marker,IDIC(Yp) |
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Authors: | Renée Bernstein MD Kathryn A. Steinhaus Mary Jo Cain |
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Affiliation: | Division of Human Genetics, Department of Pediairics, College of Medicine, University of California, Irvine. California, U.S.A. |
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Abstract: | An amniocentesis was performed at 13.3 weeks' gestation for advanced maternal age. A mosaic sex chromosome pattern was found: of 50 cells examined, 34 had a 45,X karyotype. In 14 cells with a modal number of 46, a recognizable Y was substituted by a small non-fluorescent marker. C-banding identified the marker as an isodicentric in 12 cells. In two cells, the non-fluorescent marker appeared to be monocentric and looked like a non-fluorescent del (Yq), but could have been an isodicentric Y with inactivation of one of the centromeres. Two cells with a modal number of 47 showed two copies of the monocentric marker. Fluorescent in situ hybridization with an alpha satellite Y-specific centromeric probe confirmed the Y-chromosome origin of the markers and allowed for more accurate prenatal diagnostic information. |
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Keywords: | Fluorescent in situ hybridization (FISH) Amniocentesis Anomalous sexual development Isodicentric Yp Mosaic 45,X |
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