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698例性发育异常患者染色体核型分析 被引量:1

Chromosome analysis of 698 disorders of sex development
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摘要 目的从染色体异常的角度来分析性发育异常的发病原因。方法对在湖南省计划生育研究所和长沙市妇幼保健院就诊的698例性发育异常患者采集其外周血进行染色体核型分析。结果 698例性发育异常患者中检出异常核型80例,其中染色体数目异常55例占7.88%,染色体结构异常17例占2.44%,性反转8例占1.15%。结论 698例性发育异常患者的染色体异常检出率11.46%,染色体检查可作为性发育异常的遗传学诊断方法,为治疗提供重要依据。 Objective: To investigate the causes of disorders of sex development by using statistical analysis of chromosome abnormalities.Methods: The karyotype analysis was performed on blood specimens of patients with disorders of sex development selected from The Family Planning Institue of Hunan Province and Changsha Hospital for Maternal & Child Health Care. Result: 55 cases of 698 patients showed chromosome number abnormality (7.88%) ; 17 cases showed chromosome structure aberration (2.44%) ;8 cases showed sex reversal (1.15%) . Conclusion: The detection rate of chromosome abnormalities in 698 disorders of sex development reaches 11.46%. Chromosome examination can be used for the genetic diagnosis of disorders of sex development and provide important basis for the treatment.
出处 《中国优生与遗传杂志》 2015年第6期52-53,65,共3页 Chinese Journal of Birth Health & Heredity
基金 湖南省科技厅资助项目(2011TF1011)
关键词 性发育异常 染色体 核型分析 Disorders of sex development Chromosome Karyotype
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