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作 者:石玉华[1] 陈子江[1] 张鹏[1] 盛燕[1] 高芹[1]
机构地区:[1]山东大学省立医院生殖医学中心,济南250021
出 处:《现代妇产科进展》2007年第3期199-201,共3页Progress in Obstetrics and Gynecology
摘 要:目的:探讨不孕症患者卵巢功能早衰(POF)的病因特点。方法:回顾分析符合卵巢功能早衰诊断标准的不孕症121例的病因,其中有染色体结果者45例,对其进行详细分析。结果:(1)121例不孕的卵巢功能早衰患者中,有明确发病原因者14例(11.57%),其中行卵巢手术2例,服用卵巢毒性药物或有毒物接触史3例,染色体核型异常9例;(2)原发闭经6例,继发闭经115例,原发不孕95例(78.51%),继发不孕26例(21.49%),父母系近亲结婚3例。结论:卵巢功能早衰病因中染色体异常比例较高,对卵巢功能早衰患者行染色体检查很有必要;对不孕的POF患者开展遗传学研究具有重要的意义。Objective:To explore the etiology of premature ovarian failure (POF) in infertility. Methods:One hundred and twenty one infertility cases with POF were retrospectively analyzed. There were 45 cases whose chromosome were examined. Results: ( 1 ) Fourteen POF patients had specific reasons :2 had ovarian operation;3 had taken toxico-ovary medicines and there were 9 cases with abnormal karyotype ; (2) Among the POF patients, there were 6 primary amenorrhea, 115 secondary amenorrhea ;95 primary infertility (78.51% ) ,26 secondary infertility (21.49%). Meanwhile, there were 3 patients whose parents were intermarried. Conclusions:It is necessary to examine the karyotype of POF;Genetic research on POF patients with infertility is very important.
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