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Cytogenetic Characterization of an Extra Structurally Abnormal Chromosome Associated with Severe Mental Retardation: Inv Dup (15) (q13)

机译:与严重智力发育迟缓相关的异常结构异常染色体的细胞遗传学表征:Inv Dup(15)(q13)

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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.
机译:我们已经研究了一个13岁男孩的额外结构异常染色体(ESAC),该男孩患有严重的智力,心理运动和言语障碍,行为问题,癫痫发作和脑电图异常。对带有染色体条带的双卫星ESAC的检查表明,核型为:47,XY,+ in dup(15)(pter→q13 :: q13→pter)。报道了ind dup(15)的细胞遗传学特征,特别强调了当顺序进行G带以丢弃DA / DAPI阳性染色体中可能的异质性时DA / DAPI染色的有用性,以及Ag-NOR异质性对确定inv dup(15)的母体来源。提出了两个非姐妹染色单体之间的U型交换作为其形成机理。该病例的临床特征与先前在类似病例中报道的一致。

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