Assessing the morphology and ovarian reserve of the ovaries from Mayer-Rokitansky-Küster-Hauser syndrome patients |
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作者姓名: | Ze Liang Jiali Duan Duoduo Zhang Yan You Lan Zhu |
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作者单位: | 1. Department of Obstetrics and Gynecology,National Clinical Research Center for Obstetric & Gynecologic Diseases,State Key Laboratory of Complex Severe and Rare Diseases,Peking Union Medical College Hospital,Chinese Academy of Medical Sciences & Peking Union Medical College;2. 4+4 Medical Doctor Program,Chinese Academy of Medical Sciences & Peking Union Medical College;3. Department of Pathology,Peking Union Medical College Hospital,Chinese Academy of Medical Sciences & Peking Union Medical College |
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基金项目: | the National Natural Science Foundation of China (81830043); |
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摘 要: | <正>Dear Editor,Mayer-Rokitansky-Küster-Hauser(MRKH) syndrome is a rare congenital disease characterized by the hypoplastic uterus and vagina in women with a normal female karyotype(46, XX) and phenotype. Although some genes and mutations, such as WNT4, have been reported in a small portion of MRKH syndrome patients(Biason-Lauber et al.,
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