Balanced Reciprocal Translocation in A Case of Recurrent Miscarriage

Authors

  • Ataei, Mina Department of Obstetrics and Gynecolog, Alborz University of Medical Sciences, Karaj, Iran
  • Farahani, Masoumeh Department of Obstetrics and Gynecolog, Alborz University of Medical Sciences, Karaj, Iran
  • Jamee, Mahnaz Student Research Committee, Alborz University of Medical Sciences, Karaj, Iran
  • Saee Rad , Samira Dietary Supplements and Probiotic Research Center, Alborz University of Medical Sciences, Karaj, Iran
Abstract:

Reciprocal translocation carriers have reduced fertility, increased risk of spontaneous abortion or unbalanced karyotype in their offspring. Here, we report the inheritance of a translocation between chromosomes 12 and 16 in a family with a history of five consecutive blighted ova and an offspring with three cell lines of different genotypes. We assessed parental karyotypes and identified a heterozygous reciprocal translocation in the father (46, XY.t (12; 16) (q24.12; p13.2)). The t (12; 16) is associated with fetal wastage and may play a role in the etiology of the family's miscarriage. These findings can be used as an effective tool for reproductive guidance and genetic counseling.

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Journal title

volume 10  issue 2

pages  133- 136

publication date 2021-05

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