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17种世界首报染色体异常核型遗传分析及与脆性部位关系分析 被引量:1

Genetic analysis of 17 abnormal karyotypes of the first reported in the world and the relationship between abnormal karyotypes and fragile Sites
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摘要 目的探讨不育患者中世界首报染色体异常核型与不孕不育及脆性部位的关系。方法采用外周血淋巴细胞染色体培养技术,常规G显带核型分析。结果在2911例不育患者中,共检出异常染色体核型353例,其中世界首次发现染色体异常核型17例,其中平衡易位16例,染色体臂间倒位1例。17例世界首报核型中有15个断裂位点为染色体的脆性部位,所占比例高达44.1%(15/34)。结论染色体异常是导致不良孕产、不孕不育的重要原因之一。染色体断裂位点与脆性部位有紧密的关系。 Objective To investigate the relationship between novel abnormal karyotypes and infertility in infertile patients and the relationship between abnormal karyotypes and fragile sites.Methods Chromosome specimens were made using routine culture of peripheral blood lymphocytes.Karyotyping was conducted mainly by G banding.Results 353 cases abnormal chromosomes were observed in 2911 cases of infertile patients.And 17 cases of novel abnormal karyotypes were observed,including 16 cases of balanced translocation and 1 case of pericentric inversion.15 fracture locus from 17 cases of abnormal karyotypes were chromosome fragile sites,the proportion is as high as 44.1 % (15/34).Conclusion Chromosome abnormality is one of main factors for abnormal pregnancy and infertility.There is a close relationship between chromosomal breakpoints and fragile sites.
出处 《中国实验诊断学》 2014年第2期203-205,共3页 Chinese Journal of Laboratory Diagnosis
基金 广东省计生委项目(编号:2008009)
关键词 世界首报 核型分析 脆性部位 first reported in the world karyotype fragile sites
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参考文献4

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  • 2LG Shaffer, J McGowan-Jordan, M Schmid. ISCN (2013) : an inter- national system for human cytogenetic nomenclature [ M ]. S Karger Publishers, Basel, 2013.
  • 3Speevak MD, Mc Gowan-Jordan J, Chun K. The detection of chro- mosome anomalies by QF-PCR and residual risks as compared to G- banded analysis [ J ]. Prenat Diagn ,2011,31 (5) :454-458.
  • 4McClelland LS, Allen SK, Larkins SA, et al. Implementation and experience of an ahemative QF-PCR and MLPA diagnostic strategy to detect chromosomal abnormalities in fetal and neonatal pathology samples [ J ]. Pediatr Dev Pathol,2011,14 (6) :460-468.
  • 5Wright CF, Wei Y, Higgins JP, et al. Non-invasive prenatal diag- nostic test accuracy for fetal sex using cell-free DNA a review and meta-analysis [ J ]. BMC Res Notes, 2012,5 ( 1 ) : 476-477.
  • 6Chiu RW, Akolekar R, Zheng YW, et al. Non-invasive prenatal assessment of trisomy 21 by multiplexed maternal plasma DNA se- quencing: large scale validity study [ J ]. BMJ, 2011, 6 ( 3 ) : 342-345.
  • 7Martin A, Krishna I, Martina B, et al. Can the quantity of cell-free fetal DNA predict preeclampsia:a systematic review [ J]. Prenat Di- agn,2014,34(7) :685-691.
  • 8Chiu RW. Noninvasive prenatal testing by maternal plasma DNA a- nalysis : current practice and future applications [ J ]. Scand J Clin Lab Invest Suppl,2014,74(s244) :48-53.
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