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对一名有肌强直性营养不良家族史的疑似个体及其流产胎儿进行DNA分析。

DNA analysis in a suspected individual with myotonic dystrophy family history and her abortus.

作者信息

Bi Xiaoying, Xie Huijun, Zheng Huimin, Ding Suju, Zhang Sheqing, Wang Ye, Xu Zhun, Ren Daming

机构信息

Department of Neurology, Changhai Hospital, The Second Military Medical University, Shanghai 200433, China.

出版信息

Chin Med J (Engl). 2002 Nov;115(11):1628-31.

Abstract

OBJECTIVE

To observe trinucleotide repeat number, (CTG)n in the 3'-untranslated region of the myotonic protein kinase (MTPK) gene in a clinically suspected woman with myotonic dystrophy (DM) family history and her abortus, in order to confirm the necessity of exerting antenatal examination in patients or suspected individuals with DM family history.

METHODS

Long Expand Template polymerase chain reaction (PCR) system was used to analyze CTG trinucleotide repeat numbers located in the 3' untranslated region of MTPK on chromosome 19q13.2-3 in both peripheral white cells and muscles of the suspected mother and the other two DM patients in the family. The tissues of her abortus and blood of a health woman were detected, too.

RESULTS

CTG repeats in both peripheral white cells and muscles of the suspected mother and the tissue of abortus were higher than normal range of CTG repeat number. There is no significant difference between blood and muscle samples. High CTG repeats were detected in blood and muscles of the typical DM members in the family, but in the blood sample of control, CTG repeats is normal.

CONCLUSION

CTG trinucleotide analyses and antenatal examination should be done in pregnant with a DM family history, in order to reduce the birth rate of DM offspring.

摘要

目的

观察一位临床疑似有强直性肌营养不良(DM)家族史的女性及其流产胎儿的强直性肌营养不良蛋白激酶(MTPK)基因3'-非翻译区三核苷酸重复序列(CTG)n,以确定对有DM家族史的患者或疑似个体进行产前检查的必要性。

方法

采用长片段模板聚合酶链反应(PCR)系统分析疑似母亲及其家族中另外两名DM患者外周血白细胞和肌肉中位于19q13.2 - 3染色体上MTPK基因3'非翻译区的CTG三核苷酸重复序列数。同时检测其流产胎儿的组织和一名健康女性的血液。

结果

疑似母亲外周血白细胞和肌肉以及流产胎儿组织中的CTG重复序列高于CTG重复数的正常范围。血液和肌肉样本之间无显著差异。在该家族典型DM成员的血液和肌肉中检测到高CTG重复序列,但在对照血液样本中,CTG重复序列正常。

结论

对有DM家族史的孕妇应进行CTG三核苷酸分析和产前检查,以降低DM患儿的出生率。

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