Pitfalls in prenatal diagnosis: cytogenetic analysis in amniocytes fails to detect mosaic r(12).

Autor: de Pater JM; Department of Medical Genetics, University Medical Center, Utrecht, the Netherlands. J.M.dePater@dmg.azu.nl, Scheres JM, Christiaens GC, Ausems MG
Jazyk: angličtina
Zdroj: Prenatal diagnosis [Prenat Diagn] 2003 Jan; Vol. 23 (1), pp. 65-7.
DOI: 10.1002/pd.514
Abstrakt: Objective: To review the accuracy of a prenatal diagnosis of a missed chromosomal mosaicism in amniotic fluid cell cultures and to see whether adapting the Dutch guidelines would have made any difference to the outcome in this case.
Method: Metaphases, obtained from cultured amniocytes and peripheral blood lymphocytes, were analyzed with different results. The amniocyte cultures were then reanalyzed and the risk of missing this mosaicism in prenatal analysis was assessed.
Results: The prenatal tests performed according to the Dutch guidelines showed a normal female karyotype, but more extensive postnatal analysis revealed a ring chromosome in 50% of the child's lymphocytes. Reanalysis of the original amniocytes confirmed the normal diagnosis, but when more cells from the same and other colonies were analyzed, the ring chromosome was detected.
Conclusion: The chance of missing such a supernumerary ring mosaicism is very low (about 2% in our case). Given its very rare occurrence and the low chance of it being missed if the existing Dutch guidelines are followed, adapting the number of cells or colonies to be examined for all prenatal diagnoses does not appear to be justified.
(Copyright 2003 John Wiley & Sons, Ltd.)
Databáze: MEDLINE
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