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Robertsonian Translocations: Mechanisms of Formation, Aneuploidy, and Uniparental Disomy and Diagnostic Considerations

机译:罗伯逊易位:形成,非整倍性和单亲二体的机制和诊断注意事项。

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摘要

Robertsonian translocations (ROBs) are rearrangements of the acrocentric chromosomes 13-15 and 21-22. Cytologically, ROBs between homologous chromosomes cannot be distinguished from isochromosomes that originate through duplication of a single homologue. Both types of rearrangements can be involved in aneu-ploidy. A conceptus with a trisomy or a monosomy can be rescued, and in a proportion of cases, a uniparental disomy (UPD) would result. If there are regions of genome imprinting on a uniparental chromosome pair, phenotypic consequences can result. Chromosomes 14 and 15 are imprinted, and UPD of these are known to result in abnormalities. Thus, prenatal testing should be considered in all pregnancies when one of the parents is a balanced carrier of a ROB because of the risk for aneuploidy, and UPD testing should be considered in fetuses found to carry a balanced ROB or isochromosome that involves chromosomes 14 or 15. Additionally, infants or children with congenital anomalies who carry a ROB should also be considered for UPD testing.
机译:罗伯逊易位(ROBs)是acrocentric染色体13-15和21-22的重排。从细胞学上讲,同源染色体之间的ROB不能与通过复制单个同源物而产生的同染色体区分开。两种类型的重排均可参与非整倍性。具有三体性或单体性的概念可以挽救,在某些情况下,会导致单亲二体性(UPD)。如果在单亲染色体对上有基因组印记区域,则会导致表型后果。染色体14和15上有印迹,已知其中的UPD会导致异常。因此,当所有父母中有一个父母是非平衡倍体的风险时,应在所有妊娠中考虑进行产前检查,发现携带平衡性ROB或涉及14号或16号染色体的同染色体的胎儿,应考虑进行UPD检查。 15.另外,携带ROB的先天异常婴儿或儿童也应考虑进行UPD测试。

著录项

  • 来源
    《Genetic Tsting》 |2002年第3期|p.163-168|共6页
  • 作者

    SUNG-RYUL KIM; LISA G. SHAFFER;

  • 作者单位

    Department of Clinical Pathology, Ulsan University Hospital and University of Ulsan College of Medicine, Ulsan, Korea;

  • 收录信息 美国《科学引文索引》(SCI);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 普通生物学;
  • 关键词

  • 入库时间 2022-08-17 13:27:56

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