Simultaneous Occurrence of Turner Syndrome and Robertsonian Translocation in a Girl with Short Stature: A Case Report

نویسندگان

  • Farzaneh , Mohammad Reza Department of Pathology, School of Medicine, Bushehr University of Medical Sciences, Bushehr, Iran
  • Hasanpour , Mojtaba Department of Molecular Pathology and Cytogenetics, Mehr Laboratory, Boushehr, Iran
  • Khavari , Maryam Department of Molecular Pathology and Cytogenetics, Mehr Laboratory, Boushehr, Iran
چکیده مقاله:

Short stature is an important clinical feature of Turner syndrome (TS). In this report, a girl with short stature suspected to have Turner syndrome underwent cytogenetic analysis, which confirmd Turner syndrome by observing sex chromosomal monosomy using the karyotype test. In addition to Turner syndrome, Robertsonian (ROB) translocation t(13;14) was detected. As recommended by a genetic counselor, all family members underwent karyotype analysis, which detected ROB translocation t(13;14) in father of the family. The simultaneous occurrence of ROB translocation and Turner syndrome is a rare phenomenon and affects the individual’s life, for instance, reduced fertility. Therefore, cytogenetic study is recommended in cases with abnormally short stature in order to manage their health before any treatment procedure  

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عنوان ژورنال

دوره 22  شماره 3

صفحات  184- 190

تاریخ انتشار 2019-08

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