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[一名父亲为9号染色体臂间倒位携带者的新生儿发生3号染色体长臂重复(dup 3q)]

[Duplication of the long arm of chromosome 3 (dup 3q) in a newborn infant whose the father is carrier of pericentric inversion of chromosome 9].

作者信息

Ayral D, Raudrant D, Charleux J P, Noel B

出版信息

Pediatrie. 1984 Dec;39(8):681-90.

PMID:6598632
Abstract

The authors report a case of a partial trisomy for the long arm of chromosome 3. The associated morphotypic anomalies are compared with the 31 cases already reported, and allow to further outline a well recognizable morphotype which has similarities with the Brachmann Cornelia de Lange Syndrome. The chromosomal mechanisms which may result in this unbalanced caryotype dup 3 q are discussed, and among them the possible role of a paternal chromosome 9 pericentric inversion, most commonly termed as a normal variant.

摘要

作者报告了一例3号染色体长臂部分三体的病例。将相关的形态学异常与已报道的31例病例进行了比较,进一步勾勒出一种易于识别的形态类型,它与布-科二氏综合征有相似之处。讨论了可能导致这种不平衡核型dup 3 q的染色体机制,其中包括父源9号染色体臂间倒位(最常被视为正常变异)可能发挥的作用。

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