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与严重智力障碍相关的一条额外结构异常染色体的细胞遗传学特征:inv dup(15)(q13)

Cytogenetic characterization of an extra structurally abnormal chromosome associated with severe mental retardation: inv dup (15) (q13).

作者信息

Gorla N, Slavutsky I, Lisanti J, Pedrazzini E, Vanella L, Larripa I

机构信息

Universidad Nacional de Río Cuarto (UNRC), Argentina.

出版信息

Hereditas. 1998;129(1):1-5. doi: 10.1111/j.1601-5223.1998.t01-1-00001.x.

Abstract

We have studied an extra structually abnormal chromosome (ESAC) in a 13 years old boy with profound mental, psychomotor and speech retardation, behavioral problems, seizures and abnormal electroencephalogram. The examination of the bisatellited ESAC with chromosome banding demonstrated that the karyotype was: 47, XY, +inv dup (15) (pter-->q13::q13-->pter). The cytogenetic characterization of the inv dup (15) is reported with special emphasis on the usefulness of DA/DAPI staining when G-banding is sequentially performed to discard possible heteromorphisms in DA/DAPI positive chromosomes, and the importance of Ag-NOR heteromorphisms to ascertain the maternal origin of the inv dup (15). A U-type exchange between two non-sister chromatids is proposed as its mechanism of formation. The clinical features of the case were consistent with those previously reported in similar cases.

摘要

我们对一名13岁男孩的一条结构异常额外染色体(ESAC)进行了研究,该男孩存在严重的智力、精神运动和语言发育迟缓、行为问题、癫痫发作以及脑电图异常。通过染色体显带对这条双随体ESAC进行检查,结果显示核型为:47, XY, +inv dup (15) (pter-->q13::q13-->pter)。本文报告了inv dup (15)的细胞遗传学特征,特别强调了在依次进行G显带以排除DA/DAPI阳性染色体中可能的异态性时,DA/DAPI染色的作用,以及Ag-NOR异态性对于确定inv dup (15)母源起源的重要性。本文提出其形成机制为两条非姐妹染色单体之间的U型交换。该病例的临床特征与之前类似病例报告的特征相符。

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