Assessing the morphology and ovarian reserve of the ovaries from Mayer-Rokitansky-Küster-Hauser syndrome patients  

作　　者：Ze Liang Jiali Duan Duoduo Zhang Yan You Lan Zhu 

机构地区：[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,Beijing 100730,China [2]4+4 Medical Doctor Program,Chinese Academy of Medical Sciences&Peking Union Medical College,Beijing 100730,China [3]Department of Pathology,Peking Union Medical College Hospital,Chinese Academy of Medical Sciences&Peking Union Medical College,Beijing 100730,China

出　　处：《Science China(Life Sciences)》2023年第5期1204-1207,共4页中国科学（生命科学英文版）

基　　金：supported by the Non-profit Central Research Institute Fund of Chinese Academy of Medical Sciences(2020PT320-003,2021-PT320-001);the National Natural Science Foundation of China(81830043)。

摘　　要：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.

关 键 词：Hauser UTERUS CONGENITAL 

分 类 号：R711.1[医药卫生—妇产科学]