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Constitutional Chromoanagenesis of Distal 13q in a Young Adult with Recurrent Strokes

机译:年轻人中风复发的远端13q的体质性彩色化。

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Constitutional chromoanagenesis events, which include chromoanasynthesis and chromothripsis and result in highly complex rearrangements, have been reported for only a few individuals. While rare, these phenomena have likely been underestimated in a constitutional setting as technologies that can accurately detect such complexity are relatively new to the mature field of clinical cytogenetics. G-banding is not likely to accurately identify chromoanasynthesis or chromothripsis, since the banding patterns of chromosomes are likely to be misidentified or oversimplified due to a much lower resolution. We describe a patient who was initially referred for cytogenetic testing as a child for speech delay. As a young adult, he was referred again for recurrent strokes. Chromosome analysis was performed, and the rearrangement resembled a simple duplication of 13q32q34. However, SNP microarray analysis showed a complex pattern of copy number gains and a loss consistent with chromoanasynthesis involving distal 13q (13q32.1q34). This report emphasizes the value of performing microarray analysis for individuals with abnormal or complex chromosome rear-rangements. (C) 2016 S. Karger AG, Basel
机译:仅有少数几个人报道了体质性显色事件,包括色合成和色杆菌病,并导致高度复杂的重排。这些现象虽然很少见,但在结构上可能已被低估了,因为能够精确检测这种复杂性的技术对于临床细胞遗传学的成熟领域来说是相对较新的。 G谱带不太可能准确地识别染色体合成或染色质增生,因为由于较低的分辨率,染色体的谱带模式可能会被错误地识别或简化。我们描述了一个最初被接受细胞遗传学检查的儿童为语言障碍的患者。作为一个年轻的成年人,他因中风复发而再次被转诊。进行了染色体分析,并且重排类似于13q32q34的简单重复。但是,SNP微阵列分析显示出复杂的拷贝数增加和减少模式,与涉及远端13q(13q32.1q34)的色合成相一致。该报告强调了对异常或复杂染色体重排的个体进行微阵列分析的价值。 (C)2016 S.Karger AG,巴塞尔

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