Publications (1)0 Total impact
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Article: Sperm analyses, genetic counselling and therapy in an infertile carrier of a supernumerary marker chromosome 15.
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ABSTRACT: A supernumerary marker chromosome (SMC) was analysed after lymphocyte culture of a patient with oligoasthenoteratozoospermia (OAT) before ICSI treatment. By additional molecular cytogenetic investigations the marker could be identified as a heterochromatic derivate of chromosome 15 [karyotype: 47,XY,+der(15)]. Sperm analyses by interphase FISH showed a normal monosomy 15 in 82% and an additional marker in 17% of the cells. In spite of these findings a pregnancy could not be induced. The brother of the patient showed the same chromosome abnormality and an OAT-syndrome as well. ICSI-treatment lead to a normal pregnancy and to the birth of a healthy boy. The genetic risk factors of both marker carriers are analysed in detail.Advances in Medical Sciences 02/2006; 51:31-5.
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Institutions
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2006
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Rheinische Friedrich-Wilhelms-Universität Bonn
- Institute of Human Genetics
Bonn, North Rhine-Westphalia, Germany
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