
DOUBLE TRANSLOCATION:
AN INTERESTING FAMILY HISTORY Uysal A1,*, Uludağ A2, Sılan F2, Erçelen N3, Zafer C4, Özdemir Ö2 *Corresponding Author: Assistant Professor Ahmet Uysal, Department of Obstetrics and Gynecology, Çanakkale
Onsekiz Mart University, Çanakkale, Turkey; Tel.: +90-533-263-55-40; Fax: +90-0286-263-59-56; E-mail:
drahmetuysal@hotmail.com page: 77 download article in pdf format
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Abstract
Double balanced translocations are particularly
rare and the risk of a fetus with an unbalanced chromosomal
anomaly is greater than for single translocation
carriers. In this present case, we describe
an interesting family history which included three
generations. A couple, married for 4 years, was referred
to the genetic clinic due to infertility and family
chromosome anomalies. A GTG-band chromosome
analysis indicated that the male partner’s karyotype
was 45,XY, t(3;18)(q11;ptel)t(13;14)(q10;q10). The
same double balanced translocation was found in two
others family members.
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