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猫眼综合征伴异常标记染色体,可能并非22号染色体。

Cat-eye syndrome with unusual marker chromosome probably not chromosome 22.

作者信息

Rosenfeld W, Verma R S, Jhaveri R C

出版信息

Am J Med Genet. 1984 May;18(1):19-24. doi: 10.1002/ajmg.1320180105.

Abstract

An unusual supernumerary chromosome with a single satellite on the long arm was found in a child with manifestations of the cat-eye syndrome including apparently low-set and malformed ears, preauricular tags, micrognathia, and imperforate anus. Although G-banding suggested that this extra material was chromosome 22, this was not confirmed by several other banding techniques. After examination of the parents' chromosomes, the nature and origin of this extra chromosome remains obscure. We conclude that patients previously diagnosed as having "partial trisomy 22" with incomplete cat-eye syndrome may have a different chromosome constitution when studied by various banding techniques.

摘要

在一名患有猫眼综合征表现的儿童中发现了一条不寻常的超数染色体,其长臂上有一个卫星。该儿童表现为耳朵明显低位且畸形、耳前赘生物、小颌畸形和肛门闭锁。尽管G显带提示这条额外的物质是22号染色体,但其他几种显带技术并未证实这一点。检查父母的染色体后,这条额外染色体的性质和来源仍不清楚。我们得出结论,以前被诊断为患有不完全猫眼综合征的“部分22三体”患者,在通过各种显带技术研究时,可能具有不同的染色体组成。

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