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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 relationship between Uygur primary amenorrhea and chromosomal abnormalities and to provide evidence for the diagnosis and treatment of Uygur primary amenorrhea. Methods 40 cases of Uygur primary amenorrhea patients with peripheral blood chromosome karyotype analysis. Results 40 cases of normal (46, XX) accounted for 55% (22/40); karyotype abnormalities accounted for 45% (18/40); Turner syndrome accounted for 30% (12/40), testicular feminization Expropriation accounted for 12.5% (5/40). Conclusion Chromosome karyotype is one of the causes of Uygur primary amenorrhea, so these patients should routinely make chromosome karyotype analysis.