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Interpretation of chromosome mosaicism and discrepancies in chorionic villi studies.

作者信息

Sachs E S, Jahoda M G, Los F J, Pijpers L, Reuss A, Wladimiroff J W

机构信息

Department of Clinical Genetics, University Hospital Dijkzigt, Erasmus University, Rotterdam, The Netherlands.

出版信息

Am J Med Genet. 1990 Oct;37(2):268-71. doi: 10.1002/ajmg.1320370222.

DOI:10.1002/ajmg.1320370222
PMID:2248296
Abstract

In 3,000 chorionic villi studies (CVS) 33 cases of mosaicism and 7 false-positive cell lines in all cells were seen. The mosaic cell lines were caused by aneuploidy of autosomes (13x), sex chromosomes (9x), and structural anomalies (11x). Mosaics of fetal origin were only 4 cases of trisomy 21 and one 47,XXY mosaic. In 7 cases abnormal karyotype of non-fetal origin was seen in all cells in direct studies, including trisomy 16 (3x) and trisomy 18 (2x). The combined use of direct CVS and cell cultures always uncovered the non-fetal origin of chromosome abnormalities and the study of cultured cells in all cases could have prevented 5 terminations. Complete follow-up studies demonstrated no false-negative results. Therefore, CVS can be nearly 100% accurate when both direct studies and cultures are examined in cases of mosaicism and other cell lines of possible non-fetal origin, such as trisomy 16, trisomy 18, translocation (21;21), and 45,X cells.

摘要

相似文献

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Interpretation of chromosome mosaicism and discrepancies in chorionic villi studies.
Am J Med Genet. 1990 Oct;37(2):268-71. doi: 10.1002/ajmg.1320370222.
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引用本文的文献

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False Negative NIPT Results: Risk Figures for Chromosomes 13, 18 and 21 Based on Chorionic Villi Results in 5967 Cases and Literature Review.无创产前检测假阴性结果:基于5967例绒毛取样结果及文献综述的13、18和21号染色体风险数据
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Chromosomal Mosaicism in Human Feto-Placental Development: Implications for Prenatal Diagnosis.
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J Clin Med. 2014 Jul 24;3(3):809-37. doi: 10.3390/jcm3030809.
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Uniparental disomy for chromosome 16 in humans.人类16号染色体单亲二体性
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