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一例阿姆布拉斯综合征患者8号染色体长臂的复杂细胞遗传学重排

Complex cytogenetic rearrangement of chromosome 8q in a case of Ambras syndrome.

作者信息

Tadin M, Braverman E, Cianfarani S, Sobrino A J, Levy B, Christiano A M, Warburton D

机构信息

Department of Genetics and Development, Columbia University, New York, New York 10032, USA.

出版信息

Am J Med Genet. 2001 Jul 22;102(1):100-4. doi: 10.1002/1096-8628(20010722)102:1<100::aid-ajmg1396>3.0.co;2-o.

Abstract

Ambras syndrome (AMS) is a unique form of congenital universal hypertrichosis. The syndrome has been found in association with rearrangements of chromosome 8 in two isolated cases. One of these patients was reported to have an apparently balanced paracentric inversion of chromosome 8, inv(8)(q12q22). Our cytogenetic analysis on this patient showed that the rearrangement of chromosome 8 is more complex than initially reported. We detected an insertion of the q23-q24 region into a more proximal region of the long arm of chromosome 8 as well as a large deletion in 8q23:46,XX, rea(8)(8pter-->8q13::8q23.2-->8q24.1::8q13-->8q23.1::8q24.1-->8qter). Given the large number of breakpoints and the presence of a substantial deletion, it is surprising that the proposita did not show anomalies other than these characteristic of Ambras syndrome.

摘要

阿姆布拉斯综合征(AMS)是先天性全身性多毛症的一种独特形式。在两例孤立病例中发现该综合征与8号染色体重排有关。据报道,其中一名患者有明显平衡的8号染色体臂内倒位,inv(8)(q12q22)。我们对该患者的细胞遗传学分析表明,8号染色体的重排比最初报道的更为复杂。我们检测到8号染色体长臂更靠近近端的区域插入了q23 - q24区域,以及8q23存在大片段缺失:46,XX, rea(8)(8pter-->8q13::8q23.2-->8q24.1::8q13-->8q23.1::8q24.1-->8qter)。鉴于断点数量众多且存在大量缺失,先证者除了具有阿姆布拉斯综合征的这些特征外未表现出其他异常,这令人惊讶。

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