节点文献
40例维吾尔族原发性闭经患者细胞遗传学分析
Cytogenefi c analysis of with Premary amenorrhes of the Uygur Patients in 40 cases
【摘要】 目的探讨维吾尔族原发性闭经与染色体核型异常的关系,为维吾尔族原发性闭经的诊治提供依据。方法对40例维吾尔族原发性闭经患者进行外周血染色体核型分析。结果 40例患者中核型正常(46,XX)占55%(22/40);核型异常占45%(18/40);其中Turner综合征占30%(12/40),睾丸女性化综合征占12.5%(5/40)。结论染色体核型异常是维吾尔族原发性闭经的原因之一,因此对此类患者应常规作染色体核型分析。
【Abstract】 Objective:To investigate the relation of primary amenorrhea of the Uygur and abnormal karyotype,attrempting to abtain the evidence for diagnoses and treatment of primary amenorrhea of the Uygur.Methods: Analyze the forty karyotype of primary amenorrhea of the Uygur patients.Rusults: The nomal karyotype(46,XX)of all the cases was 55%(22/40);the abnormal karyotype was 45%(18/40);30%(12/40)was the Turner syndrome,12.5%(5/40)was the testiculorr feminization syndrome.Conclusion:Abnormal karyotype may be one of the causes of Primary amenorrhea of the Uygur,so the analysis of karyotype should be a regulation to diagnose this diease.
- 【文献出处】 中国优生与遗传杂志 ,Chinese Journal of Birth Health & Heredity , 编辑部邮箱 ,2014年08期
- 【分类号】R711.5
- 【被引频次】1
- 【下载频次】40