[家族性部分Xp重复引起的男性核型儿童的多重异常]。

Kinderarztliche Praxis Pub Date : 1993-10-01
H Reichenbach, H Holland, B Thamm, T Theile
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引用次数: 0

摘要

一个患有多种异常和雌雄间性外生殖器的儿童。孩子的核型为男性,部分重复Xp。另外利用分子遗传学方法对sry区进行检测。我们回顾了文献中仅有的几个男性核型和部分重复Xp的人。如果复制定位于Xp 21- >Xp 22区域,则在表型上存在相似之处,包括性反转或两性间生殖器。这些受影响的患者是否代表一种新的综合征尚无定论。我们还在孩子的母亲身上发现了异常的x染色体。因此,在母亲目前的怀孕中,有复发的危险。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Multiple abnormalities in a child with male karyotype due to familial partial Xp duplication].

A child with multiple abnormalities and intersexual external genitals is presented. The child has a male karyotype with a partial duplication Xp. Using additionally methods of molecular genetics the SRY-region was detected. We reviewed the only few persons described in the literature with male karyotype and partial duplications Xp. There are similarities in phenotype including sex inversion or intersexual genitals if the duplication is localised in the region Xp 21-->Xp 22. Whether these affected patients represent a new syndrome is a moot point. We also found the aberrant X-chromosome in the mother of the child. In the present pregnancy of the mother there is, therefore, a risk of recurrence.

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