首页> 美国卫生研究院文献>Balkan Journal of Medical Genetics : BJMG >Prenatal Diagnosis of a New Case: De Novo Balanced Non-Robertsonian Translocation Involving t(15;22)(p11.2;q11.2)
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Prenatal Diagnosis of a New Case: De Novo Balanced Non-Robertsonian Translocation Involving t(15;22)(p11.2;q11.2)

机译:新病例的产前诊断:涉及t(15; 22)(p11.2; q11.2)的De Novo平衡非罗伯逊氏易位

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摘要

The balanced non-Robertsonian translocation (ROB) associated with acrocentric chromosomes is an unusual phenomenon. We report the case of rare non-ROB involving chromosomes 15 and 22 with cytogenetic and molecular cytogenetic findings of 46,XY,t(15;22)(p11.2;q11.2). To the best of our knowledge, t(15;22) is the first report of this breakpoint that is not the usual non-ROB. The karyotype of the chorionic villus cell was 46,XY,t(15;22)(p11.2; q11.2) from two different initial cultures. This is different from the usual non-ROB of acrocentric chromosomes. Comparative genomic hybridization has been performed to determine the chromosomal origin. Non-Robertsonian translocation associated with acrocentric chromosomes is an unusual event and only a few cases have been reported. In this study, we observed acrocentric chromosomes 15 and 22 as a rarely balanced non-ROB, where satellites of chromosome 15 translocated to chromosome 22 and part of chromosome 22 were translocated to chromosome 15. To the best of our knowledge, our patient is the first case reported in the literature for this translocation in prenatal and postnatal periods.
机译:与acrocentric染色体相关的平衡非罗伯逊易位(ROB)是一种不寻常的现象。我们报告了罕见的非ROB病例,涉及染色体15和22,具有46,XY,t(15; 22)(p11.2; q11.2)的细胞遗传学和分子细胞遗传学发现。据我们所知,t(15; 22)是此断点的第一个报告,它不是通常的非ROB。来自两种不同初始培养物的绒毛膜绒毛细胞的核型为46,XY,t(15; 22)(p11.2; q11.2)。这与通常的非中心染色体染色体的非ROB不同。已经进行了比较基因组杂交以确定染色体起源。与非中心染色体相关的非罗伯逊易位是不寻常的事件,仅报道了少数病例。在这项研究中,我们观察到了15个极染色体和22个顶极中心的非ROB平衡,其中15号染色体的卫星易位到22号染色体,而22号染色体的一部分又易位到15号染色体。据我们所知,我们的患者是文献报道的第一例病例在产前和产后均发生。

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