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机构地区:[1]新疆维吾尔自治区黄河路中医院检验科,乌鲁木齐830000 [2]新疆医科大学第一附属医院医学检验中心,830054
出 处:《中国优生与遗传杂志》2014年第8期53-54,64,共3页Chinese Journal of Birth Health & Heredity
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。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% (29./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.
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