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一名继发性闭经患者的新发X/X易位

De novo X/X translocation in a patient with secondary amenorrhea.

作者信息

Tarkan Y, Hacihanefioğlu S, Silahtaroğlu A N, Deviren A, Topçuoğlu D, Cenani A

机构信息

Genetic and Teratology Research Centre (GETAM), Cerrahpaşa Medical Faculty, Istanbul University, Turkey.

出版信息

Hereditas. 1995;122(1):19-23. doi: 10.1111/j.1601-5223.1995.00019.x.

Abstract

A 46,X,t(X;X) (qter-->p22;;p22-->qter) karyotype was found in the chromosome analysis of a 22 years old female patient with secondary amenorrhea. Further analysis with fluorescence in situ hybridization indicated that the marker chromosome had one active and one inactive centromere originating from the X chromosome. RBG-banding showed that the derivative X chromosome was preferentially inactivated in cultured lymphocytes.

摘要

在一名22岁继发性闭经女性患者的染色体分析中发现了46,X,t(X;X) (qter→p22;;p22→qter)核型。荧光原位杂交进一步分析表明,标记染色体有一个源自X染色体的活性着丝粒和一个失活着丝粒。RBG显带显示,衍生X染色体在培养的淋巴细胞中优先失活。

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