B. Eiben et al., A PROSPECTIVE COMPARATIVE-STUDY ON FLUORESCENCE IN-SITU HYBRIDIZATION(FISH) OF UNCULTURED AMINOCYTES AND STANDARD KARYOTYPE ANALYSIS, Prenatal diagnosis, 18(9), 1998, pp. 901-906
Fluorescence in situ hybridization (FISH) on uncultured amniocytes and
standard cytogenetic analysis after amniocentesis have been performed
for 904 samples. The experience with the FISH method and its clinical
relevance is described in a large clinical pilot study. Commercially
available chromosome-specific DNA probes for chromosomes 13, 18, 21, X
and Y were used. FISH assays were performed from 12 weeks of gestatio
n to the third trimester. In 96 per cent of the cases, hybridization w
as performed successfully. At least 50 nuclei for all probes could be
counted in 88 per cent of the cases and in 8 per cent between 10 and 4
9 nuclei were scored. All trisomies 13, 18 and 21 and all cases with g
onosomal aberrations were detected by FISH analysis with the exception
of one case of trisomy 21 in which hybridization failed due to techni
cal problems. Neither false-positive nor false-negative results were o
btained with the DNA probes, in complete agreement with standard cytog
enetics. In our experience, FISH is a valuable and reliable method for
rapid diagnosis. Consequences of FISH diagnosis are discussed. (C) 19
98 John Wiley & Sons, Ltd.