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QF-PCR examination of parental and meiotic origin of trisomy 21 in Central and Eastern Europe.

Authors :
Machatkova M
Brouckova M
Matejckova M
Krebsova A
Sperling K
Vorsanova S
Kutsev S
Zerova T
Arbuzova S
Krejci R
Petersen M
Macek M Sr
Source :
The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society [J Histochem Cytochem] 2005 Mar; Vol. 53 (3), pp. 371-3.
Publication Year :
2005

Abstract

Study of parental/meiotic origin of free trisomy 21 in nuclear families from Russia (70 cases), Ukraine (32 cases), and 22 from Germany revealed maternal nondisjunction in 77.3% (Germany), 93.8% (Ukraine), and 91.4% (Russia), paternal origin in 13.6%, 6.2%, and 8.6%, respectively. Maternal meiosis I errors were found in 84.4% (Ukraine), 77.1% (Russia), paternal origin in 3.1% (Ukraine), 2.9% (Russia). Maternal meiosis II errors occurred in 9.4% and 14.3% and paternal in 3.1% and 5.7% in Ukraine and Russia, respectively. No significant differences were found in maternal/paternal origin among Ukraine, Russia, Germany, and published data from other European regions.

Details

Language :
English
ISSN :
0022-1554
Volume :
53
Issue :
3
Database :
MEDLINE
Journal :
The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society
Publication Type :
Academic Journal
Accession number :
15750023
Full Text :
https://doi.org/10.1369/jhc.4B6510.2005