Literature DB >> 7145839

46,XX/46XY chromosome complement in amniotic fluid cell culture followed by the birth of a normal female child.

A Hunter, K Brierley, D Tomkins.   

Abstract

Experience indicates that the most likely explanation for a mixture of 46,XX/46,XY cells in an amniotic fluid sample is that of maternal cell contamination and that a normal male child is to be expected at birth. We report the bith of a normal female child following prenatal diagnosis of such a mixture. Extensive postnatal studies failed to reveal an XY cell line. The possible sources of the XY cell line are discussed, as are the various techniques that were applied in an effort to discover it's origin. Cross-contamination of samples could be ruled out and there was no evidence of an unsuspected twin pregnancy. It is clear from this case that not all 46,XX/46,XY results obtained in amniotic fluid can be assumed to represent maternal cell contamination and some effort should be made to eliminate other potential sources for such a mixture.

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Year:  1982        PMID: 7145839     DOI: 10.1002/pd.1970020209

Source DB:  PubMed          Journal:  Prenat Diagn        ISSN: 0197-3851            Impact factor:   3.050


  3 in total

1.  Presumptive mosaic origin of an XX/XY female with ambiguous genitalia.

Authors:  O Zuffardi; L Gargantini; S Lambiase; F Lo Curto; P Maraschio; C E Ford
Journal:  J Med Genet       Date:  1987-03       Impact factor: 6.318

2.  Twinning rate in spontaneous abortions.

Authors:  I A Uchida; V C Freeman; M Gedeon; J Goldmaker
Journal:  Am J Hum Genet       Date:  1983-09       Impact factor: 11.025

Review 3.  Clinical spectrum of female genital malformations in prenatal diagnosis.

Authors:  Michael R Mallmann; Ulrich Gembruch
Journal:  Arch Gynecol Obstet       Date:  2022-02-27       Impact factor: 2.344

  3 in total

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