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Chromosome studies in 1792 males prior to intra-cytoplasmic sperm injection: the Dutch experience.

Authors :
Tuerlings JH
de France HF
Hamers A
Hordijk R
Van Hemel JO
Hansson K
Hoovers JM
Madan K
Van der Blij-Philipsen M
Gerssen-Schoorl KB
Kremer JA
Smeets DF
Source :
European journal of human genetics : EJHG [Eur J Hum Genet] 1998 May-Jun; Vol. 6 (3), pp. 194-200.
Publication Year :
1998

Abstract

The chance of a male with severe oligozoospermia or azoospermia achieving a pregnancy has undergone a revolutionary increase with the introduction of the intracytoplasmic sperm injection technique (ICSI). However, since ICSI circumvents part of the natural sperm selection mechanisms, the possible transmission of genetic defects to the offspring is a major concern. Cytogenetic analysis is a relatively simple technique to identify at least the carriers of a chromosomal aberration before starting the ICSI procedure. In order to assess the frequency of chromosomal aberrations in male ICSI candidates, we have performed a nationwide cytogenetic study. Of the 1792 males examined, 72 (4.0%) revealed a chromosomal aberration, and one individual even had two. Numerical sex chromosomal aberrations and Robertsonian translocations predominated, followed by reciprocal translocations, inversions and supernumerary marker chromosomes. The different implications, in case a chromosomal aberration is encountered prior to ICSI, are discussed.

Details

Language :
English
ISSN :
1018-4813
Volume :
6
Issue :
3
Database :
MEDLINE
Journal :
European journal of human genetics : EJHG
Publication Type :
Academic Journal
Accession number :
9781022
Full Text :
https://doi.org/10.1038/sj.ejhg.5200193